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  • Articles  (109)
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  • Springer  (109)
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  • 1
    ISSN: 1572-879X
    Keywords: nitric oxide ; carbon monoxide ; hydrogen ; Pt/Al2O3 ; Rh/Al2O3
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The effect of adding 330–4930 ppm hydrogen to a reaction mixture of NO and CO (2000 ppm each) over platinum and rhodium catalysts has been investigated at temperatures around 200–250°C. Hydrogen causes large increases in the conversion of NO and, surprisingly, also of CO. Oxygen atoms from the additional NO converted are eventually combined with CO to give CO2 rather than react with hydrogen to form water. This reaction is described by CO + NO +3/2H2 → CO2 + NH3 and accounts for 50–100% of the CO2 formed with Pt/Al2O3 and 20–50% with Rh/Al2O3. With the latter catalyst a substantial amount of NO converted produces nitrous oxide. Comparison with a known study of unsupported noble metals suggests that isocyanic acid (HNCO) might be an important intermediate in a reaction system with NO, CO and H2 present.
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  • 2
    ISSN: 1572-879X
    Keywords: nitric oxide ; selective reduction ; Cu/ZrO2 ; sulfated-zirconia
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The selective catalytic reduction (SCR) of NO by decane under an oxidising atmosphere has been carried out on Cu/ZrO2 and Cu/ZrO2(SO 4 2− ). Zirconia-supported Cu catalysts were prepared by ligand exchange with Cu acetylacetonate followed by calcination at 773 K. The solids obtained were characterised by temperature programmed reduction (TPR) by hydrogen and temperature programmed desorption (TPD) of NO. Cu/ZrO2 is active and selective in the reduction of NO by decane at low temperature (〈 600 K) but oxidises NO to NO2 between 640 and 770 K. By contrast, whatever the temperature, a total selectivity to nitrogen is obtained with Cu/ZrO2(SO 4 2− ). About 40% NO conversion to N2 is observed with GHSV of 70 000 h−1. The promoting effect of sulfate is attributed to the large increase of acidity and the strong interaction between copper and sulfur species which is evidenced by TPD of NO and TPR by H2.
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  • 3
    ISSN: 1572-879X
    Keywords: selective catalytic reduction ; nitric oxide ; copper exchanged mordenite ; electron spin resonance (ESR)
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The effect of oxygen on the selective catalytic reduction of NO by NH3 was examined over a copper exchanged mordenite type zeolite catalyst. The catalytic activity for NO reduction by NH3 in the presence of oxygen was at least one order of magnitude higher than that in the absence of oxygen and it was fully reversible with respect to the presence of oxygen in the feed gas stream. Based upon ESR, TPD, TPO and TPSR studies, the redox behavior of copper ions was closely related to the enhancement of NO removal activity by the introduction of oxygen to the feed gases.
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  • 4
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    Catalysis letters 35 (1995), S. 165-174 
    ISSN: 1572-879X
    Keywords: nitric oxide ; rhodium ; dissociation kinetics ; static secondary ion mass spectrometry ; temperature-programmed desorption
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The desorption and dissociation of nitric oxide on a polycrystalline Rh foil were studied by means of combined temperature-programmed desorption (TPD) and static secondary ion mass spectrometry (SSIMS). The latter method was employed either under isothermal conditions or in a temperature-programmed mode (TPSSIMS). After carefully calibrating the secondary ion intensities by means of TPD, the NO dissociation kinetics were quantitatively evaluated for low NO coverages. Fitting the SSIMS data with a Polanyi-Wigner ansatz and assuming first-order kinetics, we found an activation energy,E=8±2 kJ/mol, and a preexponential,v=100.2±0.4s−1. The data were confirmed by independent isothermal SSIMS measurements at several temperatures between 80 and 330 K. The fairly unusual rate parameters are discussed in relation to similar results obtained recently from measurements on Rh single crystal surfaces.
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  • 5
    ISSN: 1572-879X
    Keywords: nitric oxide ; selective reduction ; Cu/mordenite
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract A Cu/mordenite catalyst was prepared by ion exchange and characterized by N2 Sorption, XRD, TPR by H2 and TPD by NO. The catalyst was evaluated in the selective catalytic reduction of NO by decane in O2-rich atmosphere under temperature-programmed reaction from 293 to 773 K. Two NO reduction profiles at 590 and 650 K occur under these conditions. By testing different operating protocols and different alkanes as reductants, it was concluded that the low temperature peak (590 K) is due to alkane condensed in the porosity of mordenite.
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  • 6
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    Catalysis letters 62 (1999), S. 127-130 
    ISSN: 1572-879X
    Keywords: simultaneous reduction ; sulfur dioxide ; nitric oxide ; carbon monoxide ; carbonyl sulfide ; lanthanum oxysulfide ; cobalt disulfide
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The present work reports a catalytic system for the simultaneous reduction of SO2 and NO using CO as a reducing agent. The catalyst contains lanthanum oxysulfide and cobalt sulfides. Experimental results showed that at temperature above 450°C, SO2 and NO conversions are greater than 98 and 99%, respectively.
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  • 7
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    Catalysis letters 34 (1995), S. 151-161 
    ISSN: 1572-879X
    Keywords: nitric oxide ; oxidation of nitric oxide ; H-ZSM5 catalyst ; selective catalytic reduction of nitric oxide ; pollution abatement ; automotive emissions ; active sites of H-ZSM5 catalyst
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The catalytic activities of H-ZSM5-18, H-ZSM5-150, Li-ZSM5-18, and H-Mag (numerical suffixes mark the Si/Al ratios of zeolites, H-Mag is the proton exchanged form of the layered sodium silicate, magadiite) were compared for the oxidation of NO by O2 at different ratios of reactants at reaction temperatures from 25 to 600°C. H-ZSM5-18 typically has activity maxima near 25 and 400°C at most O2/NO reactant ratios. Regardless of the partial pressures of reactants, NO±1/2O2 ⇋ NO2 equilibria are attained at 400°C and above. The H-ZSM5-150 and Li-ZSM5-18 zeolites are only active at temperatures near 25°C. H-Mag is practically inactive at the reaction conditions used. Results indicate that Lewis acidic lattice aluminium ions and silanol hydroxyls are not active in the oxidation of NO to NO2 over H-ZSM5 zeolites. Brønsted acidic bridging hydroxyls are probably active sites for this reaction at temperatures above 200°C.
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  • 8
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    Cellular and molecular life sciences 52 (1996), S. 136-140 
    ISSN: 1420-9071
    Keywords: Blood-brain barrier ; nitric oxide ; arginine ; sodium fluorescein ; N-nitro L-arginine methyl ester
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract The role of nitric oxide (NO), a well known vasodilator, in the regulation of blood-brain barrier (BBB) permeability is not clear. Therefore, the present study was planned to assess the role of NO-releasing compounds like sodium nitroprusside (SNP) and the active metabolite of molsidomine, SIN-1, as well as a precursor of NO, L-arginine, on this physiological barrier. The permeability was assessed by using several tracers. All three agents increased the permeability of BBB to the tracer. The increase in permeability caused by L-arginine was not blocked by N-nitro-L-arginine methyl ester (L-NAME). L-Arginine-treated brains did not show an elevation of nitrite content, thus ruling out the possibility of NO generation and its involvement in BBB permeability alteration. It is concluded that NO itself causes an increase in the permeability of BBB. However arginine-induced opening is not NO mediated.
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  • 9
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    Cellular and molecular life sciences 52 (1996), S. 344-347 
    ISSN: 1420-9071
    Keywords: Pancreatic islets ; DNA degradation ; streptozotocin ; nicotinamide ; nitric oxide
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract The impact of short term in vitro exposure to the diabetogenic drug streptozotocin on pancreatic islet glucose metabolism, insulin secretion, DNA fragmentation and cell viability, was studied. Streptozotocin impaired cell viability as well as insulin secretion and the oxidation of glucose. These effects were partially counteracted by inhibition of the inducible form of nitric oxide synthase with N-monomethyl-arginine and by scavenging oxygen free radicals with nicotinamide. Isolated islets underwent double strand DNA fragmentation after 24 h in culture. The degree of DNA breakdown was strongly enhanced by exposure of the islet DNA was obtained with N-monomethyl-arginine and nicotinamide. These data suggest that the generation of reactive oxygen and nitrogen species is involved in the deleterious action of streptozotocin on pancreatic islet tissue. A role for oxygen radicals generated during streptozotocin-induced islet cell damage as possible mediators of the expression of the inducible form of nitric oxide synthase and the scavenging action of nicotinamide on these radicals, is then proposed.
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  • 10
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    Cellular and molecular life sciences 51 (1995), S. 99-105 
    ISSN: 1420-9071
    Keywords: Alzheimer's disease ; chromosomes 14, 19, 21 ; amyloid β-protein ; spirochetes ; tau protein ; choline transporter ; cholinergic neurons ; acetylcholinesterase inhibitors ; tacrine ; antioxidants ; free radicals ; nerve growth factor (NGF) ; indomethacin ; apoptosis ; nitric oxide
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract Alzheimer's disease is the most common type of progressive and debilitating dementia affecting aged people. In some early — as well as late-onset familial cases, a genetic linkage with chromosomes 14, 21 (early-onset) or 19 (late-onset) has been indicated. Furthermore, a direct or indirect role has been attributed to normal or structurally altered amyloid β-protein (concentrated in senile plaques) and/or excessively phosphorylated tau protein (located in neurofibrillary tangles). Degeneration of cholinergic neurons and concomitant impairment of cortical and hippocampal neurotransmission lead to cognitive and memory deficits. Several compounds are being tested in attempts to prevent and/or cure Alzheimer's disease, including tacrine, which has very modest efficacy in a sub-group of patients, and new acetylcholinesterase inhibitors. Pilot experiments have also been launched using nerve growth factor (NGF) to prevent or stabilize the processes of cholinergic pathway degeneration. Alternatively, antioxidants, free radical scavengers and/or non steroidal anti-inflammatory agents may be screened as potential therapies for neurodegenerative diseases induced by multiple endogenous and/or exogenous factors. The recent use of transgenic mice, in parallel with other genetic, biochemical and neurobiological systems, in vivo and/or in vitro (cell cultures), should accelerate the discovery and development of specific drugs for the treatment of Alzheimer's disease.
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  • 11
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    BioMetals 9 (1996), S. 10-14 
    ISSN: 1572-8773
    Keywords: ferritin ; iron release ; nitric oxide ; S-nitrosothiol
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Abstract It has been previously reported that iron release from ferritin could be promoted by nitric oxide (NO) generated from sodium nitroprusside. It was thus proposed that some of the toxic effects of NO could be related to its ability to increase intracellular free iron concentrations and generate an oxidative stress. On the contrary, the iron exchange experiments reported here show that NO from S-nitrosothiols is unable to promote iron release from ferritin. The discrepancy may be explained by the disregarded ability of ferrozine, the ferrous trap used in the previous report, to mobilize iron both from ferritin and from sodium nitroprusside spontaneously.
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  • 12
    ISSN: 1572-8773
    Keywords: nitric oxide ; cisplatin ; NOS ; renal toxicity
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Abstract Cisplatin treatment of rats results into a significant increase in the activity of Ca2+-independent nitric oxide synthase (NOS) in kidneys and liver. Significant enhancement of lipid peroxidation in gastric mucosa, kidneys and liver was also observed. The administration of N G-nitro-l-arginine methyl ester, an inhibitor of NOS, markedly reduced renal and gastrointestinal toxicity, and also decreased the content of blood urea nitrogen, serum creatinine, and incidence of diarrhoea along with a significant inhibition in lipid peroxidation in the target organs. The present report, while demonstrating the beneficial effect of the blockade of NO pathways during cisplatin chemotherapy, may be helpful in developing strategies for combating some of the toxic side-effects of the drug.
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  • 13
    ISSN: 1572-879X
    Keywords: silver ; silver sulfate ; alumina ; nitric oxide ; catalytic reduction
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract A new Ag/Al2O3 catalyst for removing NOx in diesel engine exhaust gas was developed. The influence of SO2 on the reduction of lean NOx by ethanol over the Ag/Al2O3 catalyst was evaluated in simulated diesel exhaust and characterized using TPD, XRD, XPS, SEM and BET measurements. The Ag/Al2O3 catalyst was highly active for the reduction of NOx with ethanol in the presence of SO2 although the reduction of NOx is suppressed at lower temperatures. The activity for NOx reduction is high even on the Ag/Al2O3 catalyst exposed to a SO2 (200 ppm)/O2 (10%)/H2O (10%) flow for 20 h at 723 K and comparable to that on the fresh Ag/Al2O3 catalyst. No crystallized Ag metal and Ag compounds were formed by the SO2/O2/H2O exposure. On the other hand, crystallized Ag2SO4 was easily formed when the Ag/Al2O3 catalyst was exposed to a SO2 (200 ppm)/O2 (10%)/NO (800 ppm)/H2O (10%) flow for 10 h at 723 K. XRD, SEM and XPS studies showed that the formation of crystallized Ag2SO4 results in growing of Ag particles in larger size and lowering the surface content of Ag particles. In addition, the specific surface area of the Ag/Al2O3 catalyst decreases from 221 to 193 m2/g. Although the dispersion of Ag particles was decreased by the formation of Ag2SO4, the activity for the reduction of lean NOx was, remarkably, not affected. This suggests that the Ag–alumina sites created by the Ag2SO4 formation are still active for the lean catalytic reduction of NOx.
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  • 14
    ISSN: 1572-879X
    Keywords: nitrous oxide ; nitric oxide ; reduction ; propane ; Fe-MFI ; platinum
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Solid-state ion exchange in the presence of air has been used to prepare Fe-MFI catalysts that exhibit activities comparable to preparations obtained under anaerobic conditions. Preliminary results obtained during the simultaneous catalytic reduction of NO and N2O with propane in the temperature range from 473 to 773 K show that Fe-MFI might be of interest for the treatment of exhaust gases containing NOx and nitrous oxide. Undesirable CO formed in a side-reaction can be oxidized to CO2 by promotion of Fe-MFI with small amounts of Pt.
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  • 15
    ISSN: 1572-879X
    Keywords: selective catalytic reduction ; nitric oxide ; ammonia ; Mn‐promoted silica–alumina
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Deactivated (waste) silica–alumina sorbents were carbonized and used as supports. The introduction of manganese led to active and selective SCR catalysts at low temperatures. Two methods of Mn promoting were compared: wet impregnation and adsorption. They influenced the distribution of Mn and N2O production. The catalysts behaved similarly to Mn‐promoted active carbon.
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  • 16
    ISSN: 1572-8773
    Keywords: Cu-PuPy ; Cu2Zn2 superoxide dismutase ; diSchiff base Cu SOD mimetic copper complex ; nitric oxide
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Abstract In addition to the well known catalytically accelerated O2 dismutation, Cu2Zn2 Superoxide dismutase (SOD) reversibly reduces NO to NO− with the consequence of a prolonged half-life of NO. This alternative reactivity was examined in the presence of the intact CuZn enzyme and a diSchiff base copper complex prepared from putrescine and pyridine-2-aldehyde (Cu-PuPy) which is known as a convenient active center analog of the former copper protein. The reaction of this SOD mimick with NO and NO− was monitored by electronic absorption and electron paramagnetic resonance (EPR) spectroscopy via the formation of nitrosylmyoglobin. Cu-PuPy reacted up to three times faster with NO compared with Cu2Zn2 SOD and 15 times faster in comparison with CuSO4 and copper EDTA. The oxidation rate of NO− by Cu-PuPy was up to 300% higher compared with the reactivities of CuSO4 and Cu EDTA. Cu2Zn2SOD reacted with NO− to a neglible extent only. Catalytic characteristics could be observed in the course of the oxidation of NO− in concentrations between 1 and 20 μM copper. Disturbances of the EPR properties suggested a modification of the chemical environment at the copper sites in both the copper complex and the enzyme. As a consequence, no further reactions of the nitrogen monoxides with the respective active centers were seen. In conclusion, Cu-PuPy appears to be an efficient moderator of the biochemical reactivity of nitrogen monoxides attributable to the observed increased half-life of NO.
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  • 17
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    European journal of clinical pharmacology 49 (1996), S. 335-339 
    ISSN: 1432-1041
    Keywords: Migraine ; Histamine ; nitric oxide ; glyceryl trinitrate ; cerebral arteries ; transcranial Doppler
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Medicine
    Notes: Abstract It has previously been shown that in migraine sufferers infusion of glyceryl trinitrate (GTN) and histamine causes an immediate headache during the infusion and a genuine migraine attack one to several hours after the infusion. This identical time profile indicates a common mechanism of action. To evaluate whether GTN causes headache via liberation of histamine, we studied the effect of GTN 0.5 ώg · kg−1·min−1 for 20 min in seven migraine sufferers, once after pretreatment with the histamine-1(H1)-receptor blocker mepyramine (0.5 mg · kg−1) and once without pretreatment. This mepyramine dose is known to completely abolish histamine-induced headache. After pretreatment with mepyramine five patients experienced migraine, and without pretreatment six patients did so. The median peak headache score was 7 on a 0–10 scale with and without mepyramine pretreatment. The arterial responses, evaluated with transcranial Doppler, were also unaffected by the mepyramine pretreatment. Our results demonstrate that neither headache nor arterial dilatation due to GTN infusion is caused by histamine release. In all likelihood the common mediator of migraine induction by GTN and histamine is nitric oxide.
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  • 18
    ISSN: 1573-4919
    Keywords: nitric oxide ; carbon monoxide ; ischemia ; heart ; intracellular signaling ; cGMP ; SOD
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Abstract To examine the intracellular signaling mechanism of NO in ischemic myocardium, isolated working rat hearts were made ischemic for 30 min followed by 30 min of reperfusion. A separate group of hearts were pre-perfused with 3 mM L-arginine in the presence or absence of 650 μM of protoporphyrin, a heme oxygenase inhibitor for 10 min prior to ischemia. The release of NO was monitored using an on-line amperometric sensor placed into the right atrium. The aortic flow and developed pressure were examined to determine the effects of L-arginine on ischemic/reperfusion injury. Induction for the expression of heme oxygenase was studied by Northern hybridization. For signal transduction experiments, sarcolemmal membranes were radiolabeled by perfusing the isolated hearts with [3H] myoinositol and [14C] arachidonic acid. Biopsies were processed to determine the isotopic incorporation into various phosphoinositols as well as phosphatidic acid and diacylglycerol. cGMP was assayed by radioimmunoassay and SOD content was determined by enzymatic analysis. The release of NO was diminished following ischemia and reperfusion and was augmented by L-arginine. L-arginine reduced ischemic/reperfusion injury as evidenced by the enhanced myocardial functional recovery. Protoporphyrin modulated the effects of L-arginine. cGMP, which was remained unaffected by ischemia and reperfusion, was stimulated significantly after L-arginine treatment. The NO-mediated augmentation of cGMP was reduced by protoporphyrin suggesting that part of the effects may be mediated by CO generated through the heme oxygenase pathway. Reperfusion of ischemic myocardium resulted in significant accumulation of radiolabeled inositol phosphate, inositol bisphosphate, and inositol triphosphate. Isotopic incorporation of [3H] inositol into phosphatidylinositol, phosphatidylinositol-4-phosphate, and phosphatidylinositol-4,5-bisphosphate was increased significantly during reperfusion. Reperfusion of the ischemic heart prelabeled with [14C] arachidonic acid resulted in modest increases in [14C] diacylglycerol and [14C] phosphatidic acid. Pretreatment of the heart with L-arginine significantly reversed this enhanced phosphodiesteratic breakdown during ischemia and early reperfusion. However, at the end of the reperfision the inhibitory effect of L-arginine on the phosphodiesterases seems to be reduced. In L-arginine treated hearts, SOD activity was progressively decreased with the duration of reperfusion time. The results suggests for the first time that NO plays a significant role in transmembrane signaling in the ischemic myocardium. This signaling appears to be on- and off- nature, and linked with SOD content of the tissue. The signaling is transmitted via cGMP and opposes the effects of phosphodiesterases by inhibiting the ischemia/reperfusion-induced phosphodiesteratic breakdown. Our results also suggest that NO activates heme oxygenase which further stimulates the production of cGMP presumably by CO signaling. Thus, NO not only potentiates cGMP mediated intracellular signaling, it also functions as a retrograde messenger for CO signaling in heart.
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  • 19
    ISSN: 1573-4919
    Keywords: nitric oxide ; oxygen radicals ; tocopherol ; vasodilation ; aging rat
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Abstract Acetylcholine-induced, endothelium-dependent relaxation of norepinephrine-precontracted aortic strips, was severely impaired after exposure to a hypoxanthine/xanthine oxidase reaction generating oxygen radicals. This effect was more evident in aortic strips of aging rats (24 months old) in comparison to young rats (3 months old). The addition of authentic ·NO (1 μM) completely relaxed aortic strips exposed to oxidative stress both in young and aging rats. In vitro EPR measurements showed that the ·NO signal was reduced by enzymatic O2-generating reaction. The activity of a partial purified preparation of constitutive NO synthase from rat cerebellum was significantly decreased after exposure to exogenous oxygen radicals. Pretreatment of aortic strips with 100 μM alpha-tocopherol-phosphate, produced a significant improvement of acetylcholine-dependent relaxation in the aortic strips exposed to oxidative stress, particularly in the aged vessel. The content of malondialdehyde in aortic tissue did not change after oxidative stress or alpha-tocopherol pretreatment. Alpha-tocopherol was unable to recover the NO synthase activity depressed in vitro by hypoxanthine/xanthine oxidase reaction. This study confirms that an oxidative stress impairs the endothelium-mediated vasodilation. Alpha-tocopherol pretreatment protects the vessel against this damage. The mechanism of action of alpha-tocopherol is unknown, but seems unrelated to an antioxidant activity.
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  • 20
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    Molecular and cellular biochemistry 157 (1996), S. 23-30 
    ISSN: 1573-4919
    Keywords: cyclic GMP ; nitric oxide ; natriuretic peptides ; guanylyl cyclase ; cardiomyocytes ; endothelium
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Abstract The second messenger cGMP is a major intracellular mediator of the vaso-active agents nitric oxide and natriuretic peptides. The principal targets of cGMP are (i) phosphodiesterases, resulting in interference with the CAMP-signalling pathway, (ii) cGMPgated cation channels, and (iii) cGMP-dependent protein kinases (cGKs). Only two mammalian isotypes of cGK have been described so far: type I cGK, consisting of an α and a β isoform, presumably splice variants of a single gene, and identified as the most prominent cGK isotype in the cardio-vascular system; and type II cGK, expressed mainly in the intestine, the kidney and the brain. High levels of cGK I are found in vascular smooth muscle cells, endothelial cells and platelets. In these cells, cGK I is thought to counteract the increase in contraction provoked by Ca-mobilizing agonists, to reduce endothelial permeability and to inhibit platelet aggregation, respectively. Relatively low levels of cGK I are found in cardiomyocytes. In this cell type, cGK is implicated in the negative inotropic effect of cGMP, presumably through modulation of Ca channels and by diminishing the Ca-sensitivity of contractile proteins.
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  • 21
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    Molecular and cellular biochemistry 163-164 (1996), S. 291-303 
    ISSN: 1573-4919
    Keywords: septic cardiomyopathy ; cardiomyocyte ; endotoxin ; nitric oxide ; tumor necrosis factor α ; cardiodepressant factor (CDF)
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Abstract In the multiple organ dysfunction syndrome of sepsis and septic shock the heart is one of the organs subject to failure. Many new insights into the mechanisms underlying septic cardiomyopathy were gained in the last years. Experimental work with neonatal and adult cardiomyocytes considerably contributed to this progress, facilitating the documentation of direct attenuation of the contractions of the heart muscle cell by toxins and mediators, as well as investigating the underlying cellular mechanisms. With this respect, contractile-depressant effects have been found in cardiomyocytes for many toxins and sepsis mediators, with endotoxin, Pseudomonas exotoxin A, tumor necrosis factor a, interleukin-1 and nitric oxide being the most relevant ones identified. These substances interfere at clinically relevant concentrations with several main inotropic axes, not only with the β-adrenoceptor/adenylyl cyclase and with the NO-cGMP-system — on which most of the interest is focused at present — but also with the α1-adrenoceptor/phosphoinositide pathway and the Ca2+ homeostasis of the cardiomyocyte, the latter representing the common final inotropic pathway. Not a single cardiodepressant factor, but more likely a total bunch of toxins and mediators with different attack mechanisms seem to contribute to the picture of septic cardiomyopathy.
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  • 22
    ISSN: 1573-4919
    Keywords: nitric oxide ; human lymphocyte ; immunoglobulins ; oxygen free radical scavenger
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Abstract We investigated the role of endogenous or exogenous nitric oxide (NO) on human lymphocyte function. We used sodium nitroprusside, nitroglycerine, S-nitroso-N-acetylpenicillamine, sodium nitrite and S-nitroso-L-glutathione as NO-generating compounds. All agents were used at doses that do not produce direct cytotoxicity as measured by trypan blue exclusion as well as chromium-51 release assay. The immune responses examined were peripheral blood lymphocytes (PBL) proliferation and IL-2 production after activation with OKT3 and PHA; allogeneic mediated proliferation and cell mediated cytotoxicity (CML) in MLR; IgG and IgM production after PBL activation with Con-A; proliferation and expression of IFN-γ and IL-4 mRNA after activation of allogeneic CD4+T cell clones. Cytokine mRNA expression was measured by reverse transcriptase PCR. Our results show that proliferating lymphocytes do not produce a detectable amount of NO as measured by the Griess reaction. In separate experiments, on of NG-monomethyl-L-arginine (L-NMMA) did not affect lymphocyte proliferation. Sodium nitroprusside and nitroglycerine exerted a dose dependent antimitogenic effect, inhibited cytokine production and expression, CML generation and antibody production. DNA gel electrophoresis showed no evidence for enhanced programmed cell death. The antimitogenic effect could not be blocked by the NO scavengers, hemoglobin or methylene blue. In contrast, the other nitric oxide generating compounds did not inhibit lymphocyte mitogenesis. The results suggest that human lymphocytes do not produce appreciable amounts of NO to affect lymphocyte mitogenesis. Sodium nitroprusside and nitroglycerine have a potent but nonspecific immunoinhibitory effect on human lymphocyte function by a mechanism other than NO production. In addition, pharmacological levels of NO do not inhibit human lymphocyte mitogenesis.
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  • 23
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    Molecular and cellular biochemistry 159 (1996), S. 7-14 
    ISSN: 1573-4919
    Keywords: coronary circulation ; heart ; hydrogen peroxide ; nitric oxide ; oxidative stress ; vasodilation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Abstract Oxidative stress mediated by hydrogen peroxide (H2O2) increases coronary flow (CF) in Langendorff-perfused rat hearts. We investigated the possible role of nitric oxide (NO) in H2O2-induced vasolidation. A dose-response study was conducted to find a concentration of H2O2 which increased CF without influencing left ventricular developed (LVDP) or end-diastolic (LVEDP) pressures. 80 (n = 10),100 (n = 7), 120 (n = 7),140 (n = 7),160 (n = 7), and 180 (n = 10) μM H2O2 was infused for 10 min, followed by recovery for 50 min. 80 μM H2O2 increased CF to a maximum of 143 ± 4 (mean ± S.E.M) percent of initial value after 15 min observation (p 〈 0.001 compared to buffer only), with no effect on LVDP or LVEDP. Another series of hearts were perfused with N-nitro-L-Arginine methylester (L-NAME, 1 μM), methylene blue (MB, 50 μM), or haemoglobin (Hb, 10 μM), without (n = 7 in each) or with (n = 10 in each) 80 μM H2O2 for 10 min. L-NAME, MB, and Hb alone increased CF, but attenuated the H2O2-induced increase of CF. LVDP was depressed when L-NAME, MB, or Hb were given in conjunction with 80 μM H2O2. In summary, H2O2 concentration-dependently increased LVEDP and depressed LVDP. The H2O2-induced increase of CF was independent of concentration. Inhibition of NO synthesis, action, or soluble guanylate cyclase attenuated the H2O2-induced increase of CF, and depressed LVDP when given together with H2O2. H2O2 induces a NO-dependent vasodilation, and inhibition of NO is detrimental to left ventricular function after H2O2-mediated oxidative stress.
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  • 24
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    Molecular and cellular biochemistry 179 (1998), S. 99-110 
    ISSN: 1573-4919
    Keywords: diaphragm ; oxygen-derived free radicals ; respiratory muscle fatigue ; nitric oxide ; sarcoplasmic reticulum ; calcium
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Abstract It is now recognized that respiratory muscle fatigue contributes to the development of respiratory failure in some patients with lung disease. This observation has prompted an examination into the mechanisms of development of muscle fatigue, with the understanding that an elucidation of these processes may lead to new therapeutic approaches to the treatment of these patients. A series of recent studies examining this issue have, moreover, discovered that oxygen-derived free radicals generated during strenuous contraction may modulate respiratory muscle contractile function and contribute to the development of muscle fatigue. The data supporting this concept include: (a) direct (e.g. EPR, ESR studies) and indirect (evidence of lipid peroxidation, protein carbonyl formation, glutathione oxidation) evidence that there is heightened free radical production in contracting muscle, (b) evidence that pharmacologic depletion of muscle antioxidant stores increases degree of muscle fatigue present after a period of exercise, and (c) evidence that administration of agents that act as free radical scavengers retard the development muscle fatigue. Free radicals may produce these changes in muscle force generating capacity by interacting with and altering the function of a number of intracellular-biophysical processes (i.e. sarcolemmal action potential propagation, sarcoplasmic reticulum calcium handling, mitochondrial function, contractile protein interactions).
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  • 25
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    Molecular and cellular biochemistry 179 (1998), S. 125-134 
    ISSN: 1573-4919
    Keywords: diaphragm ; respiratory muscle contraction ; nitric oxide ; sepsis ; endotoxin ; cytokine ; oxygen-derived free radicals
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Abstract It became evident in the past 12 years that venitlatory muscle contractile performance is significantly impaired during the course of septic shock. In animal models of septic shock, depression of ventilatory muscle contractile performance has been shown to cause hypercapneic ventilatory failure and respiratory arrest. Failure of ventilatory muscle contractility in septic shock has never been attributed to a single factor, but two groups of factors are likely to be involved: (a) increased ventilatory muscle metabolic demands due to augmentation of ventilation, hypoxemia and increased pulmonary impedance; and (b) specific cellular, metabolic, immune and hemodynamic defects which interfere with several processes necessary for normal force generation. These defects are mediated by complex interactions between several local and systematic mediator such a bacterial endotoxin, proinflammatory cytokines, prostaglandins, platelet activating factor, reactive oxygen species and nitric oxide. This is a summary of how these interactions are likely to interfere with ventilatory muscle contractile performance in septic shock with particular emphasis on the newly described role of nitric oxide.
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  • 26
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    Keywords: pacing ; preconditioning ; farnesol ; high-cholesterol diet ; nitric oxide ; electron spin resonance ; rat heart
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Abstract We have previously shown that hypercholesterolemia leads to the loss of pacing-induced preconditioning (PC), possibly due to the impairment of cardiac nitric oxide (NO) synthesis. It has been shown that excess exogenous cholesterol inhibits formation of several polyprenyl derivatives involved in signal transduction. In the present study, we examined whether PC and cardiac NO synthesis are restored by treatment with the key polyprenyl product, farnesol, in cholesterol-fed rats. Rats fed 2% cholesterol-enriched/control diet for 24 weeks were given i.p. 5 μM/kg farnesol/vehicle, respectively. An hour later, hearts were isolated and prepared for ‘working’ perfusion, then subjected to PC/non-PC protocols of 3 intermittent periods of pacing of 5 min duration at 10 Hz, followed by a 10 min coronary occlusion to test the effect of PC. PC increased ischemic aortic flow (AF) from its control value of 15.6 ± 1.5 to 27.3 ± 1.7 mL/min (p 〈 0.05). PC was not observed in hearts obtained from hypercholesterolemic rats (AF: 15.7 ± 1.2 mL/min), however, it reappeared in the farnesol-treated hypercholesterolemic group (AF: 31.8 ± 3.4 mL/min, p 〈 0.05). In tissue samples from the left ventricle, cholesterol-diet markedly decreased the intensity of the electron spin resonance spectra of NO obtained after in vivo spin trapping with Fe2+-diethyl-dithio-carbamate complex. Farnesol-treatment did not influence cardiac NO content in the cholesterol-fed or in the control group. These results show that the lost PC can be recaptured by farnesol-treatment in hypercholesterolemia, however, farnesol-treatment does not restore cardiac NO synthesis.
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  • 27
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    Molecular and cellular biochemistry 188 (1998), S. 103-111 
    ISSN: 1573-4919
    Keywords: diabetes ; myocardium ; oxygen derived radicals ; vitamin E ; transcription factor NF-κB ; endothelium ; nitric oxide ; lipid peroxidation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Abstract The evidence that the generation of reactive oxygen intermediates (ROI) plays an important role for the increased cardiovascular risk in diabetes is summarised. In addition to the well known parameters of oxidative stress as lipid hydroperoxides and thiobarbituric acid substances (TBARS), recent observations indicate that isoprostanes which can be taken as a more specific parameter of oxidative, are generated in higher amounts by diabetic patients. This increased formation of isoprostanes can be inhibited by an instalment of a close metabolic control or the supplementation with tocopherol. The cause for the elevated oxidative stress is not yet fully understood, however the autoxidation of glucose, the formation of advanced glycation endproducts and the activation of NADPH-oxidase seem to be relevant processes. Since ROI are able to quench nitric oxide and to inhibit the synthesis of prostacyclin, the antithrombotic, vasodilating and antiatherosclerotic properties of endothelium are impaired in diabetes. Additionally, the balance of endothelial mediators released by endothelium is shifted to angiotensin II and endothelin, compounds which enhance the proliferation of smooth muscle cells and may limit the coronary reserve of myocardium. The activation of the transcription factor NF-κB by glucose and its autoxidative products is regarded as a key event in the transformation of the vasculature in diabetes. Epidemiological observations and very recent clinical studies underlie the impact of ROI for the development of cardiovascular complications in diabetes and suggest that an antioxidative treatment might be helpful to reduce the cardiac risk in diabetes.
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  • 28
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    Molecular and cellular biochemistry 160-161 (1996), S. 159-166 
    ISSN: 1573-4919
    Keywords: reactive oxygen species ; 8-hydroxy-2′-deoxyguanosine ; heart ; nitric oxide ; aging ; rat
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Abstract Biochemical and structural changes occurring in the myocardium with aging are mainly resulting from the association of a general tissue atrophy with the hypertrophy of the remaining myocytes. Whilst hypertrophy seems to be a compensatory process to the loss of cardiomyocytes and to a mild systolic hypertensive condition that accompanies elderly people, atrophy should be the modification more closely related to aging ‘per se.’ In support to the free radical theory of aging, several signs of oxidative damage have been shown in the aged heart, such as lipofuscin accumulation, decreased phospholipid unsaturation index, greater formation of both hydrogen peroxide and 8-hydroxy-2′deoxyguanosine. As a compensatory reaction, the activities of the main oxygen-radical scavenger enzymes are stimulated in the mitochondria of aged rat heart. Endothelium-mediated vasoregulation is more susceptible to oxidative stress in aged with respect to young rats, suggesting that also the vasculature can be negatively influenced by the oxygen free radicals generated during aging. The possible primary role of oxygen free radicals in the development of myocardial atrophy is also discussed.
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  • 29
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    Keywords: atria contractility ; protein kinase C ; nitric oxide ; muscarinic cholinergic receptors ; chagasic IgG
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    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Abstract We have already demonstrated the presence of antibodies in the sera of chagasic patients with the ability to interact with neurotransmitter receptors triggering several intracellular pathways of transduction signals. Here we show that, chagasic IgG induced protein kinase C (PKC) translocation to rat cardiac membranes and this effect was inhibited by muscarinic cholinergic blockers atropine and AF-DX 116 pointing to the participation of M2 receptors in this effect. It was also able to stimulate nitric oxide synthase (NOS) activity and this action was blunted by phospholipase C (PLC) and PKC inhibitors indicating that the production of nitric oxide (NO) would be the consequence of the cascade of enzymatic pathways triggered by mAChR activation. PKC and NOS activities were involved in chagasic IgG negative inotropic actions on rat isolated myocardium as its effects were blunted by staurosporine and L-N-monomethyl arginine. Furthermore, low concentrations of chagasic IgG inhibited the cardiac mechanical action of carbachol in a non-competitive manner. These data suggested that PKC activation in myocardium by chagasic IgG would be involved in its physiological actions by modulating NOS activity. The participation of PKC-mediated phosphorylation of mAChR leading to receptor desensitization as one of the causes of dysautonomia is also discussed.
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  • 30
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    Molecular and cellular biochemistry 168 (1997), S. 87-93 
    ISSN: 1573-4919
    Keywords: nitric oxide ; superoxide dismutase ; macrophages
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    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Abstract Rat peritoneal macrophages stimulated with lipopolysaccharide (LPS) and Phorbol myristate acetate (PMA) generated increased levels of superoxide anions (O2ú-) by 122% as compared to those stimulated with PMA alone. However, Nitric oxide (NO) synthase inhibitors-n-monomethyl arginine (nMMA) or spermine-HCI lowered the enhanced levels of O2ú- released by LPS treated macrophages. The Superoxide dismutase (SOD) activity in LPS treated macrophages was 51% lower than that observed in resident cells. NO synthase inhibitors prevented the loss of SOD activity in LPS treated cells. Exogenously added SOD during sensitization of cells with LPS also inactivated the enzyme. This inactivation of SOD is inhibited by Nitric oxide synthase inhibitors. PMA alone did not affect SOD activity. NO synthase inhibitors also did not affect PMA activated superoxide anion generation in macrophages. These studies indicate that nitric oxide generated by LPS treated macrophages can inactivate SOD activity.
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  • 31
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    Keywords: nitric oxide ; endotoxin ; cardiomyocytes ; guanosine 3′, 5′-cyclic monophosphate ; calcium ; ADP-ribosylation ; phosphorylation
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    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Abstract To evaluate the effects of the in vivo endotoxin treatment of the rat on (1) the contractile responses in the subsequently isolated papillary muscle to adrenergic and cholinergic agonists and (2) the biochemical parameters (cyclic GMP, nitric oxide synthesis, protein phosphorylation and ADP-ribosyslation) in the subsequently isolated cardiomyocytes. Following the in vivo endotoxin treatment (4 mg/kg i.p., 18 h), contractile responses to increasing amounts of isoprenaline or to increasing amounts of oxotremorine in the presence of a fixed amount of isoprenaline were determined in isolated papillary strips. Activities of nitric oxide synthase, guanylyl cyclase, as well as phosphorylation of phospholamban and troponin-inhibitory subunit, and pertussis toxin-catalyzed and endogenous ADP-ribosylations were determined in the intact cardiomyocytes and subcellular fractions. The increase in the force of contraction by isoprenaline was reduced, while its inhibition by oxotremorine was greater in the endotoxin-treated papillary strips. The activities of both nitric oxide synthase, primarily of the inducible form of the enzyme, and cytosolic guanylyl cyclase were higher while the phosphorylations of both phospholamban and troponin-inhibitory subunit were of lesser magnitude in the cardiomyocytes following the in vivo endotoxin treatment. Pertussis toxin-catalyzed ADP-ribosylation of the 41 kDa polypeptide, which is the alpha subunit of Gi, was also decreased. The results of the present study support the postulate that alterations in both the cyclic AMP and cyclic GMP signalling cascade contribute to the myocardial dysfunction caused by endotoxin and cytokines.
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  • 32
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    Keywords: nitric oxide ; MPTP ; 3-nitropropionic acid ; malonate ; 3-nitrotyrosine ; free radicals
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    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Abstract Excitotoxicity, mitochondrial dysfunction and free radical induced oxidative damage have been implicated in the pathogenesis of several different neurodegenerative diseases, such as amyotrophic lateral sclerosis, Parkinson's disease (PD), Alzheimer's disease (AD), and Huntington's disease. Much of the interest in the association of neurodegeneration with mitochondrial dysfunction and oxidative damage emerged from animal studies using mitochondrial toxins. Within mitochondria 1-methyl-4-phenylpyridinium (MPP+), the active metabolite of 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP), acts to inhibit NADH-coenzyme Q reductase (complex I) of the electron transport chain. MPTP produces Parkinsonism in humans, primates, and mice. Similarly, lesions produced by the reversible inhibitor of succinate dehydrogenase (complex II), malonate, and the irreversible inhibitor, 3-nitropropionic acid (3-NP), closely resemble the histologic, neurochemical and clinical features of HD in both rats and non-human primates. The interruption of oxidative phosphorylation results in decreased levels of ATP. A consequence is partial neuronal depolarization and secondary activation of voltage-dependent NMDA receptors, which may result in excitotoxic neuronal cell death (secondary excitotoxicity). The increase in intracellular Ca2+ concentration leads to an actiation of Ca2+ dependent enzymes, including the constitutive neuronal nitric oxide synthase (cnNOS) which produces NO·. NO· may react with the superoxide anion to form peroxynitrite. We show that systemic administration of 7-nitroindazole (7-NI), a relatively specific inhibitor of cnNOS in vivo. attenuates lesions produced by striatal malonate injections or systemic treatment with 3-NP or MPTP. Furthermore 7-NI attenuated increases in lactate production and hydroxyl radical and 3-nitrotyrosine generation in vivo, which may be a consequence of peroxynitrite formation. Our results suggest that neuronal nitric oxide synthase inhibitors may be useful in the treatment of neurologic diseases in which excitotoxic mechanisms play a role. (Mol Cell Biochem 174: 193–197, 1997)
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  • 33
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    Keywords: ischemia-reperfusion ; nitric oxide ; spin trapping ; EPR ; nitrosyl iron complex ; dithiocarbamates
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    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Abstract Spin-trapping techniques combined with electron paramagnetic resonance (EPR) spectroscopy to measure nitric oxide (·NO) production were compared in the ischemic-reperfused myocardium for the first time, using both aqueous-soluble and lipophilic complexes of reduced iron (Fe) with dithiocarbamate derivatives. The aqueous-soluble complex of Fe and N-methyl-D-glucamine dithiocarbamate (MGD) formed MGD2-Fe-NO complex with a characteristic triplet EPR signal (aN12.5 G and giso = 2.04) at room temperature, in native isolated rat hearts following 40 min global ischemia and 15 min reperfusion. Diethyldithiocarbamate (DETC) and Fe formed in ischemic-reperfused myocardium the lipophilic DETC2-Fe-NO complex exhibiting an EPR signal (g⊥ = 2.04 and g∥ = 2.02 at 77K) with a triplet hyperfine structure at g⊥. Dithiocarbamate-Fe-NO complexes detected by both trapping agents were abolished by the ·NO synthase inhibitor, NG-nitro-L-arginine methyl ester. Quantitatively, both trapping procedures provi ded similar values for tissue ·NO production, which were observed primarily during ischemia. Postischemic hemodynamic recovery of the heart was not affected by the trapping procedure. (Mol Cell Biochem 175: 91–97, 1997)
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  • 34
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    Keywords: endothelium ; polymorphonuclear leukocyte ; nitric oxide ; intimal hyperplasia ; P-selectin
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    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Abstract The effects of an anti-P-selectin monoclonal antibody (MAb, PB1.3; Cytel Corporation) on neoendothelialization; neoendothelial function, as evidenced by acetylcholine-induced relaxation (nitric oxide formation); and intimal hyperplasia following embolectomy catheter-induced injury to the rabbit thoracic aorta were investigated. Catheter injury was induced in two groups of New Zealand White rabbits. One group received no treatment, while the second group received short-term treatment with the MAb (i.p., immediately before and 12 h after induction of catheter injury). A third group underwent a sham operation and served as uninjured controls. Following sacrifice at 2 weeks after injury, aortic rings were assessed for degree of intimal hyperplasia, neoendothelial morphology (scanning electron microscopy), and acetylcholine-induced relaxation. Aortic tissue from catheter-injured animals that received treatment exhibited improved neoendothelial morphology, as compared with tissue from untreated but catheterized animals; however, no statistically significant attenuation of the hyperplastic response or improvement in the attenuated neoendothelial-dependent acetylcholine-induced relaxant response that is characteristic of neoendothelium that forms after catheter denudation was observed. These data suggest that short-term attenuation of P-selectin-mediated polymorphonuclear leukocyte (PMN)/endothelium, PMN/platelet interactions, and/or thrombin formation beneficially affects neoendothelialization of the vascular wall following balloon catheter-induced injury.
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  • 35
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    Molecular and cellular biochemistry 157 (1996), S. 137-145 
    ISSN: 1573-4919
    Keywords: endothelium ; nitric oxide ; endothelium-derived hyperpolarising factor ; feedback inhibition ; intracellular pH ; tyrosine kinases ; tyrosine phosphatases ; shear stress ; monocyte chemoattractant protein-1
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Abstract Coronary vascular endothelial cells control vascular tone by modulating the local concentration of circulating vasoactive substances (e.g. adenine nucleotides, biogenic amines and bradykinin) and by synthesising and releasing the vasoactive autacoids nitric oxide (NO) and prostacyclin (PGI2). The fluid shear stress exerted by the streaming blood is the physiologically most important stimulus for a continuous endothelial NO production, which counteracts neuro- and myogenic constriction. This shear stress-dependent NO release represents a highly effective local system for maintaining adequate blood flow to the myocardial tissue. At the transcriptional level endothelium-derived NO modulates the regulation of a number of genes (e.g. monocyte chemoattractant protein-1, P-selectin and vascular cell adhesion molecule-1) most probably by direct and/or indirect interaction with transcription factors. In addition to NO and PGI2, the coronary vascular endothelium is also able to release a factor which causes hyperpolarisation of the underlying smooth muscle. This so-called endothelium-derived hyperpolarising factor (EDHF) displays the characteristics of a cytochrome P450-derived arachidonic acid metabolite. However, since NO is able to attenuate production of this factor, EDHF may contribute to the regulation of vascular tone essentially in situations associated with an apparent dysfunction of the endothelium.
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  • 36
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    Keywords: nitric oxide ; preconditioning ; reperfusion arrhythmias ; isolated rat heart ; SIN-1 ; glyceryl trinitrate ; adenosine ; nitric oxide toxicity
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Abstract NO has been implicated in the mechanism of ischaemic preconditioning. To verify this hypothesis further we have attempted to reproduce effects of ischaemic preconditioning by nitric oxide donors administration prior to the ischaemia. The effect of glyceryl trinitrate (GTN) and 3-morpholino-sydnonimine-hydrochloride (SIN- 1), NO donors, on reperfusion induced ventricular tachycardia (VT) and ventricular fibrillation (VF) in Langendorff perfused rat hearts subjected to 10 min regional ischaemia followed by 10 min reperfusion were examined. Results: GTN, 500 μM and SIN-1, 10 μM, administered for 5 min and washed for another 5 min prior to ischaemia (to mimic ischaemic preconditioning), almost completely abolished reperfusion induced VF. GTN and SIN-1, administered at the time of reperfusion, increased the incidence of sustained VF and the duration of VT and VF. When given 5 min before the ischaemia and throughout the ischaemia and the reperfusion, SIN-1 abolished VF. Adenosine, 10 μM, applied according to the above three protocols, did not affect reperfusion arrhythmias, although adenosine induced changes in coronary flow and post-ischaemic reflow were similar to those produced by the NO donors. In conclusions: (1) NO is able to mimic the effect of ischaemic preconditioning on reperfusion arrhythmias in rat heart, supporting the view that NO may be one of the endogenous substances triggering ischaemic preconditioning; (2) In crystalloid-perfused heart, NO may be deleterious when its administration is restricted to the reperfusion period.
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  • 37
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    Keywords: nitric oxide ; tetrahydrobiopterin ; lipopolysaccharide ; cytokine ; myocardium
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Abstract Induction of the inducible isoform of nitric oxide (NO) synthase (iNOS) in the myocardium is implicated as a mechanism in the development of cardiac depression in immune activated states associated with an enhanced release of cytokines, such as septic shock. We evaluated the in vivo synthesis of NO and tetrahydrobiopterin (BH4), a cofactor of NOS, in the heart tissue using a model of LPS injection in rats (LPS: 10 mg/kg, i.v.). In control rats, iNOS activity or iNOS mRNA in the heart was negligible. Three hours after LPS administration, a marked induction of iNOS mRNA and activity was observed in the heart. A significant increase in BH4 content and GTP cyclohydrolase mRNA abundance was also observed in the heart from LPS-treated rats. Our results demonstrate induction of NO synthesis and parallel increase in BH4 concentration in the heart of rats after LPS treatment in vivo and may provide molecular evidence responsible for the increased production of BH4 which may up-regulate iNOS activity in the heart in vivo. (Mol Cell Biochem 166: 177-181, 1997)
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  • 38
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    Molecular and cellular biochemistry 174 (1997), S. 189-192 
    ISSN: 1573-4919
    Keywords: nitric oxide ; mitochondria ; inflammation ; respiration ; astrocytes ; cytochrome oxidase
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Abstract Nitric oxide (NO) at high levels is cytotoxic, and may be involved in a range of inflammatory, neurodegenerative, and cardiovascular/ischaemic pathologies. The mechanism of NO-induced cytotoxicity is unclear. Recently we and others have found that low (nanomolar) levels of NO reversibly inhibit mitochondrial respiration by binding to the oxygen binding site of cytochrome oxidase in competition with oxygen. This raises the apparent Km for oxygen of mitochondrial respiration into the physiological range, potentially making respiration sensitive to the oxygen level. The NO inhibition of oxygen consumption was seen in isolated cytochrome oxidase, mitochondria, brain nerve terminals, and cultured cells. Cultured astrocytes activated to express the inducible form of NO synthase produced up to 1 µM NO and strongly inhibited their own cellular respiration rate. This respiratory inhibition was rapidly reversed by removing the NO, and was due to the inhibition of cytochrome oxidase. These results suggest that any cell producing high levels of NO will inhibit its own respiration and that of surrounding cells, and make the respiration rate sensitive to the oxygen level. This inhibition of energy metabolism may contribute to cytotoxity or cytostasis in some pathologies. (Mol Cell Biochem 174: 189–192, 1997)
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  • 39
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    Molecular and cellular biochemistry 149-150 (1995), S. 249-256 
    ISSN: 1573-4919
    Keywords: arginine ; nitric oxide ; uptake ; synaptosomes ; cerebellum ; cortex
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Abstract The characteristics of the high-affinity uptake of [3H]-L-arginine into cerebellar and cortical synaptosomes were investigated. Uptake into cerebellar synaptosomes was often greater than that seen in cortical synaptosomes under similar experimental conditions, and this was reflected by a higher Vmax in synaptosomes from this brain region. Uptake into synaptosomes prepared from both brain regions was markedly enhanced by removing extracellular Na+, and inhibited by high concentrations of extracellular K+. Depolarisation with 4-aminopyridine or veratridine had no effect on uptake. Uptake was also unaffected by hyperpolarisation. The profile of inhibition of arginine uptake by related amino acids was similar to that seen for the y+ carrier, but the other characteristic alluded to above suggest that the carrier is distinct from the classical y+ system. The possible relationship between the carrier and the metabolism of arginine through the nitric oxide [NO] pathway, and the role of NO in the central nervous system is discussed.
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  • 40
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    Molecular and cellular biochemistry 149-150 (1995), S. 257-262 
    ISSN: 1573-4919
    Keywords: cyclic GMP ; hormones ; oxygen-radicals ; nitric oxide ; hemeproteins ; calcium/calmodulin
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    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Abstract The broad objective of these studies was to understand the nature of cyclic GMP system and the mechanism(s) whereby hormone, autacoids and drugs alter this signal in various physiological systems. Studies were undertaken on the modulation of guanylate cyclase activity by oxygen-radicals/nitric oxide and the mechanism(s) of generation of nitric oxide by receptor-selective hormones. We observed that cytosolic guanylate cyclase undergoes significant stimulation in the presence of oxygen-radicals/nitric oxide. This activation by nitric oxide can be reversed by hemeproteins, thus, enabling guanylate cyclase system to cycle between activated and deactivated state. The evidence is presented that oxygen-radicals are required for the synthesis of nitric oxide by NO synthase as demonstrated by inhibition of NO formation by oxygen-radical scavengers. And finally, the data is presented that acetylcholine-induced elevations of intracellular levels of cyclic GMP can be attenuated by muscarinic antagonist, atropine and superoxide anion scavenger, nitroblue tetrazolium. These observations establish a novel concept that activation of hormone receptors on the cell surface, triggers generation of oxygen radicals and hydrogen peroxide which participates in the catalytic conversion of L-arginine to nitric oxide by nitric oxide synthase in the presence of calcium ion. The oxygen-radicals/NO, thus formed, oxidatively activate guanylate cyclase and transduce the message of calcium-dependent hormones.
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  • 41
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    Keywords: human endothelial cells ; erythromycin ; calcium ion ; nitric oxide ; constitutive nitric oxide synthase ; cyclic AMP-dependent protein kinase
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Abstract A 14-membered ring macrolide, erythromycin, acts not only as an antibacterial but also as an anti-inflammatory agent. We have previously reported that erythromycin modulates neutrophil functions and ameliorates neutrophil-induced endothelial cell damage through the action of cyclic AMP-dependent protein kinase (PKA) and nitric oxide (NO). We investigated the effect of erythromycin on human endothelial cell functions. Erythromycin enhanced intracellular calcium ion concentration ([Ca2+]i) of endothelial cells and NO release from endothelial cells. The enhancement of NO release from endothelial cells by erythromycin was abolished by addition of EGTA in the medium and was partially reduced by addition of H-89, an inhibitor of PKA. These results suggest that erythromycin enhances NO release from endothelial cells through the action of PKA and [Ca2+]i. In addition, constitutive NO synthase (cNOS) protein expression of endothelial cells was dose-dependently enhanced by treatment with erythromycin, which might also contribute to the enhancement of NO release from endothelial cells by erythromycin. The effect of erythromycin as an anti-inflammatory agent might be partially mediated through the enhancement of NO release from endothelial cells and the drug might be a useful tool for the investigation of cNOS of endothelial cells.
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  • 42
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    Keywords: HL-60 cells ; differentiation ; cGMP-dependent protein kinase ; nitric oxide ; cGMP
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Abstract We previously described the isolation of a variant subline of HL-60 cells that does not differentiate in response to nitric oxide (NO)-generating agents or to cGMP analogs [7]. The variant cells have normal guanylate cyclase activity and normal NO-induced increases in the intracellular cGMP concentration. We now show that the variant cells have normal cGMP-dependent protein kinase (G-kinase) activity, both by an in vitro and in vivo assay, and using two-dimensional gel electrophoresis we have identified six G-kinase substrates in the parental cells. Of these six proteins, we found considerably less phosphorylation of one of the proteins in the variant cells than in parental cells, both in vitro and in intact cells, and by 35S-methionine/35S-cysteine incorporation we found much less of this protein in the variant cells than in parental cells. The protein is a shared substrate of cAMP-dependent protein kinase (A-kinase); since cAMP analogs still induce differentiation of the variant cells, it appears that the NO/cGMP/G-kinase and cAMP/A-kinase signal transduction pathways share some but not all of the same target proteins in inducing differentiation of HL-60 cells.
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  • 43
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    Molecular and cellular biochemistry 202 (1999), S. 141-147 
    ISSN: 1573-4919
    Keywords: (Na,K)-ATPase ; Na+-binding site ; nitric oxide ; hypertension ; L-NAME ; cardiac sarcolemma
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Abstract In the cardiovascular system, NO is involved in the regulation of a variety of functions. Inhibition of NO synthesis induces sustained hypertension. In several models of hypertension, elevation of intracellular sodium level was documented in cardiac tissue. To assess the molecular basis of disturbances in transmembraneous transport of Na+, we studied the response of cardiac (Na,K)-ATPase to NO-deficient hypertension induced in rats by NO-synthase inhibition with 40 mg/kg/day NG-nitro-L-arginine methyl ester (L-NAME) for 4 four weeks. After 4-week administration of L-NAME, the systolic blood pressure (SBP) increased by 36%. Two weeks after terminating the treatment, the SBP recovered to control value. When activating the (Na,K)-ATPase with its substrate ATP, no changes in Km and Vmax values were observed in NO-deficient rats. During activation with Na+, the Vmax remained unchanged, however the KNa increased by 50%, indicating a profound decrease in the affinity of the Na+-binding site in NO-deficient rats. After recovery from hypertension, the activity of (Na,K)-ATPase increased, due to higher affinity of the ATP-binding site, as revealed from the lowered Km value for ATP. The KNa value for Na+ returned to control value. Inhibition of NO-synthase induced a reversible hypertension accompanied by depressed Na+-extrusion from cardiac cells as a consequence of deteriorated Na+-binding properties of the (Na,K)-ATPase. After recovery of blood pressure to control values, the extrusion of Na+ from cardiac cells was normalized, as revealed by restoration of the (Na,K)-ATPase activity. (Mol Cell Biochem 000: 000-000, 1999)
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    Molecular and cellular biochemistry 200 (1999), S. 51-57 
    ISSN: 1573-4919
    Keywords: smokeless tobacco ; apoptosis ; nitric oxide
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Abstract Smokeless tobacco usage is, a growing public health concern in the United States. Lesions of the oral cavity have been clearly linked to smokeless tobacco use. The objective of this study was to determine the biochemical effects of smokeless tobacco extract (STE) exposure upon hamster cheek pouch cell (HCPC-1) cultures. HCPC-1 cells were exposed to a 5 -fold dose-range of STE (0.5, 1.0 and 2.5%) over a time-course of 24-96 h. Following each exposure we measured various biochemical parameters of cell proliferation and cell death. Cell viability, cell cycle progression and S-phase DNA synthesis were measured as markers of cell proliferation. We measured lactate dehydrogenase leakage as a marker of cell membrane damage and cell death due to necrosis. No significant alterations were observed in cell cycle progression and cell proliferation as a result of exposure to STE. LDH measured colorimetrically indicated no significant effect with the lower doses (0.5, 1.0 and 2.5% STE). Apoptosis measured as the A0 peak and by the TUNEL procedure revealed that STE caused significant rates of apoptosis. Maximal apoptosis was noted between 48-96 h. In order to probe the mechanism further we measured the levels of nitrites as an indicator of nitric oxide (NO) in the media. NO levels were significantly elevated at the doses that caused an induction of apoptosis. The results from this study indicate that STE causes a dose-dependent induction of apoptosis and that this is mediated by nitric oxide.
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  • 45
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    Molecular and cellular biochemistry 200 (1999), S. 27-33 
    ISSN: 1573-4919
    Keywords: skin ; wound ; nitric oxide ; collagen ; rat
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Abstract Nitric oxide (NO) is a messenger molecule which regulates many physiological functions like immunity, vascular tone and serves as a neurotransmitter. Although it is known to participate in healing process, its role in collagen synthesis is not clear. Therefore, the present investigation was done to study the role of NO in wound collagen synthesis. Rats received full thickness, circular (8 mm), transdermal wounds which were treated with NO releaser, sodium nitroprusside (SNP, 0.001 100 μM) topically for 5 days. Wound collagen content estimated in terms of hydroxyproline (HP) and confirmed histochemically was decreased significantly by all SNP doses. L-Arginine, a substrate for nitric oxide synthase (NOS) when applied topically decreased collagen content of the wounded tissues. N-Nitro-L-arginine methyl ester (L-NAME), a competitive inhibitor of NOS, increased wound collagen content significantly as compared to untreated and SNP treated animal wounds when administered intraperitoneally at the doses 3, 10 and 30 mg/kg. Furthermore, histological findings also demonstrated laying down of thick collagen bundles and proliferation of fibroblasts together with prominent angiogenesis in L-NAME treated wound tissues as compared to untreated and SNP treated tissues. N-nitro-D-arginine methyl ester, an inactive isomer, was found to have no effect on wound collagen levels. When L-arginine was administered in L-NAME pretreated rats, it significantly elevated wound HP content. The results indicate that NO plays an important role in regulating the collagen biosynthesis in skin model of a healing wound.
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  • 46
    ISSN: 1573-4919
    Keywords: adrenomedullin (ADM) ; calcitonin gene-related peptide (CGRP) ; vasodilation ; nitric oxide
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Abstract Vasodilator responses to human adrenomedullin (hADM), a newly discovered hypotensive peptide, human calcitonin gene-related peptide-α (hCGRP-α) and hCGRP-β, which share structural homology with hADM, were compared in the hindlimb vascular bed of the cat under constant flow conditions. Injections of hADM (0.003-1 nmol), hCGRP-α, and hCGRP-β (0.003-0.3 nmol) into the perfusion circuit caused dose-related decreases in hindlimb perfusion pressure. Vasodilator responses to hCGRP-α and hCGRP-β were similar in potency and duration, and the doses of hCGRP-α and hCGRP-β required to reduce hindlimb perfusion pressure 40 mm Hg (ED40 mm Hg) were significantly lower than the ED40 mm Hg for hADM. The duration of the hindlimb vasodilator responses to hCGRP-α and hCGRP-β were significantly longer than the duration of the response to hADM. Amylin, a peptide that shares structural homology with ADM and with CGRP, had no significant effect on hindlimb perfusion pressure when injected in doses up to 1 nmol. Decreases in hindlimb perfusion pressure in response to hADM, hCGRP-α, and hCGRP-β were not altered by L-N5-(1-iminoethyl)-ornithine (L-NIO) in a dose of the nitric oxide synthase inhibitor that decreased the vasodilator response to acetylcholine or by the cyclooxygenase inhibitor, meclofenamate, in a dose that decreased the vasodilator response to archidonic acid. The present data demonstrate that hADM, hCGRP-α, and hCGRP-β have potent, but relatively short-lasting, vasodilator activity, and that vasodilator responses are not dependent on the release of nitric oxide or vasodilator prostaglandins in the hindlimb vascular bed of the cat.
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  • 47
    ISSN: 1573-4919
    Keywords: nitric oxide ; superoxide ; hydroxyl radical ; free radicals ; SIN 1 ; sodium nitroprusside
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Abstract Nitric oxide (NO·) is a free radical characterized by a high spontaneous chemical reactivity with many other molecules including the superoxide radical (O2·−). This complex interaction may generate a peroxynitrite anion (ONOO−), which behaves as an important mediator of oxidative stress in many pathological states. In the present study, in vitro experiments were performed to assess directly the O2·− and hydroxyl (·OH) radical scavenging effects of various NO· donor drugs, i.e. sodium nitroprusside (SNP), sodium nitrite (NaNO2), molsidomine and SIN 1, at pH 7.4, 7 or 6. Concentrations of NO· in the incubation medium containing the different NO· donor drugs were measured by the assay based on the reaction of Fe-N-methyl-D-glucamine dithiocarbamate (MGD) with NO· that yields a stable spin-adduct measured by electron paramagnetic resonance (EPR). O2·− and ·OH generation was characterized by EPR spin trapping techniques, using the spin trap 5,5-dimethyl-1-pyrroline-1-oxide (DMPO). These free radicals were generated from the enzymatic system xanthine-xanthine oxidase, in phosphate buffer adjusted at pH 7.4, 7 and 6. Under these experimental conditions, SNP exhibited the strongest superoxide scavenging properties, characterized by IC50 values expressed in the µmolar range, which decreased at low pH. Addition of SNP (800 µM) to solution containing MGD and Fe2+ (5:1) at pH 7 4 produced a three line EPR spectrum which is identified to [(MGD)2-Fe2+-NO]. In control experiments no EPR signal was observed. We obtained the same results with NaNO2 and an augmentation of the spin-adduct level was noted with the prolongation of the incubation period. In return, molsidomine (2 mM) did not produce, in our conditions, a detectable production of NO·. NaNO2 displayed a significant superoxide scavenging effect only at pH 6, whilst neither molsidomine nor SIN 1 had any effect. Therefore, the superoxide scavenging properties of SNP, NaNO2, and molsidomine appeared to be closely related to their potential for NO· release, which partially depends on the pH conditions. The behaviour of SIN 1 is more complicated, the speed of oxygen diffusion probably acting as a limiting factor in NO· formation in our conditions. The production of NO· was detected in presence of SIN 1. The intensity of the complex is comparable with the signal founded with NaNO2. By contrast, all molecules exhibited hydroxyl radical scavenging properties, highlighting the capacity of ·OH to react with a wide range of molecules. In conclusion, considering the poor chemical reactivity of O2·−, the NO· donor drugs/O2·− interactions suggest a special relationship between these two radical species, which, in certain pathological states, could lead to the generation of cytotoxic end-products with strong oxidizing properties.
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  • 48
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    Molecular and cellular biochemistry 183 (1998), S. 25-38 
    ISSN: 1573-4919
    Keywords: corticotrophin ; nitric oxide ; metyrapone ; L-arginine ; L-NMMA ; nitric oxide synthase inhibitors ; neurosteroids ; anxiety ; behavior
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Abstract The nitric oxide (NO) synthase inhibitor NG-monomethyl-L-arginine (N-NMMA) and the competitive substrate for NO synthase L-arginine were used to determine the role of endogenous NO on the behavioral and neuroendocrine responsiveness following systemic corticotrophin in dexamethasone-suppressed rats. Corticotrophin (50-200 mU/kg, s.c.) dose-dependently decreased behavioral activity in the actimeter and produced significant anxiolytic and anti-risk activity in the plus-maze behavior test, without affecting systolic blood pressure. Rats given corticotrophin showed significant increased plasma corticosterone and reduced adrenal ascorbic acid level. These behavioral and adrenal responses of corticotrophin were dose dependently blocked by metyrapone (20 and 50 mg/kg, i.p.), an inhibitor of steroid 11β-hydroxylase in adrenal and neural tissues that block steroidogenesis. Intracerebroventricular administration of L-NMMA (20 μg/rat in 10 μl) significantly prevented the behavioral hypoactivity and anxiolytic-like responses of corticotrophin without influencing the adrenal responsiveness. The effect of L-NMMA was completely reversed by preadministration of L-arginine (300 mg/kg, i.p.). These results suggest that neuronal nitric oxide pathway plays an important modulating role in the behavioral effects of corticotrophin by mechanisms other than those involving cardiovascular effects.
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  • 49
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    Molecular and cellular biochemistry 196 (1999), S. 3-12 
    ISSN: 1573-4919
    Keywords: ischemia ; preconditioning ; adenosine ; protein kinase C ; KATP channel ; free radicals ; heat shock proteins ; antioxidants ; nitric oxide
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Abstract Preconditioning is a phenomenon, where brief periods of stress such as ischemia, heat shock or certain pharmacological agents make the heart tolerant to subsequent lethal ischemic injury. Preconditioning seems to involve a variety of stress signals which include activation of membrane receptors and signaling molecules such as protein kinase C, mitogen-activated protein kinases, opening of ATP-sensitive potassium channel and expression of a number of protective proteins. In this review, the potential role of these mechanisms is discussed.
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  • 50
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    Molecular and cellular biochemistry 196 (1999), S. 125-132 
    ISSN: 1573-4919
    Keywords: fever ; E. coli lipopolysaccharide ; dithiothreitol ; methylene blue ; nitric oxide ; malondialdehyde ; biothiols ; glutamate ; NMDA-receptor ; oxidative stress
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Abstract Immediately after bacterial endotoxin (LPS) enters the circulatory system there is increased production of free oxygen radicals by cells of the reticulo-endothelial system, followed by the release of cytokines considered as putative endogenous pyrogens. Fever originates by central nervous system activities, but neither exogenous nor endogenous pyrogens are able to cross the blood-brain barrier and the true signal which is transmitted to structures inside the blood-brain barrier is still unknown. To study the role of oxygen radicals in fever, we pretreated rats with methylene blue, an inhibitor of superoxide and hydroxyl radical production and investigated the febrile response to LPS in conscious rats by measuring malondialdehyde formation as an index of lipid peroxidation by oxygen radicals. Methylene blue lowered resting malondialdehyde levels to near detection level and significantly suppressed its rise which was regularly found following LPS in the untreated state. Pretreatment with methylene blue completely blocked the febrile response. Since fever is a central nervous system-mediated response these results indicate that the brain is able to sense oxidative stress and vicinal thiol groups of the redox-modulatory site of the N-methyl-D-aspartate (NMDA) subtype of glutamate receptor-channel complex could function as a possible receptive structure. To test this hypothesis we injected rabbits with the disulfide reducing agent dithiothreitol (DTT), known to penetrate the blood-brain barrier, and monitored its effect on normal and febrile body temperatures. DTT induced, independently of ambient temperature, within minutes and dose-dependently the full pattern of heat loss responses causing a fall of core temperature, indicative of a lowered thermoregulatory setpoint. Pretreatment with a bolus dose of 5 mg/kg DTT, followed by a continuous infusion of 5 mg/kg/h for 3 h completely prevented LPS-induced fever. A bolus dose of 20 mg/kg DTT, starting 30 min after LPS, immediately reversed the febrile cold defense pattern and lowered body temperature. We conclude that DTT reduces in the central nervous system oxidized vicinal thiol groups of NMDA receptors, thereby augmenting glutamate-induced nitric oxide synthase activation, and, thus, enhanced formation of NO, which, in turn, lowers the thermoregulatory setpoint. Reduction of other disulfide-containing molecules, especially oxidized glutathione and thiol-containing enzymes, by DTT by might additionally contribute to preventing fever.
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  • 51
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    The protein journal 17 (1998), S. 255-260 
    ISSN: 1573-4943
    Keywords: Heme ; hemopexin ; nitric oxide ; hemolysis ; ischemia
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Hemopexin, which acts as an antioxidant by binding heme (K d 〈 1 pM), is synthesized by hepatic parenchymal cells, by neurons of the central and peripheral nervous systems, and by human retinal ganglia. Two key regulatory molecules, nitric oxide (·NO) and carbon monoxide (CO), both bind to heme proteins and since ferroheme–hemopexin binds CO, the possible role of heme–hemopexin in binding ·NO was investigated. ·NO binds rapidly to hemopexin-bound ferroheme as shown by characteristic changes in the Soret and visible-region absorbance spectra. Circular dichroism spectra of ·NO–ferroheme-hemopexin in the Soret region exhibit an unusual bisignate feature with a zero crossover at the absorbance wavelength maximum, showing that exciton coupling is occurring. Notably, the ·NO complex of ferroheme–hemopexin is sufficiently avid and stable to allow hemopexin to bind this molecule in vivo and, thus, hemopexin may protect against NO-mediated toxicity especially in conditions of trauma and hemolysis.
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  • 52
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    Bioscience reports 19 (1999), S. 51-71 
    ISSN: 1573-4935
    Keywords: Cell signaling ; nitric oxide ; vasculation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Abstract The properties of nitric oxide as an endogenous cell signaling molecule in vascular biology are described.
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  • 53
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    Bioscience reports 19 (1999), S. 133-154 
    ISSN: 1573-4935
    Keywords: Cell signalling ; nitric oxide ; vasculature
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Abstract The role of nitric oxide in cellular signaling in the past 22 years has become one of the most rapidly growing areas in biology with more than 20,000 publications to date. Nitric oxide is a gas and free radical with an unshared electron that can regulate an ever-growing list of biological processes. In many instances nitric oxide mediates its biological effects by activating guanylyl cyclase and increasing cyclic GMP synthesis from GTP. However, the list of effects of nitric oxide that are independent of cyclic GMP is also growing at a rapid rate. For example, nitric oxide can interact with transition metals such as iron, thiol groups, other free radicals, oxygen, superoxide anion, unsaturated fatty acids and other molecules. Some of these reactions result in the oxidation of nitric oxide to nitrite and nitrate to terminate its effect, while other reactions can lead to altered protein structure, function, and/or catalytic capacity. These diverse effects of nitric oxide that are either cyclic GMP dependent or independent can alter and regulate important physiological and biochemical events in cell regulation and function. Nitric oxide can function as an intracellular messenger, an autacoid, a paracrine substance, a neurotransmitter, or as a hormone that can be carried to distant sites for effects. Thus, it is a unique simple molecule with an array of signaling functions. However, as with any messenger molecule, there can be too little or too much of the substance and pathological events result. Some of the methods to regulate either nitric oxide formation, metabolism, or function have been in clinical use for more than a century as with the use of organic nitrates and nitroglycerin in angina pectoris that was initiated in the 1870's. Current and future research with nitric oxide and cyclic GMP will undoubtedly expand the clinicians' therapeutic armamentarium to manage a number of important diseases by perturbing nitric oxide and cyclic GMP formation and metabolism. Such promise and expectations have obviously fueled the interests in these signaling molecules for a growing list of potential therapeutic applications.
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  • 54
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    Bioscience reports 19 (1999), S. 235-251 
    ISSN: 1573-4935
    Keywords: Endothelium derived relaxing factor (EDRF) ; nitric oxide
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Abstract The discovery, early studies and identification of endothelium-derived relaxing factor (EDRF) as nitric oxide, are described.
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  • 55
    ISSN: 1573-675X
    Keywords: Apoptosis ; beta cells ; cytokines ; Islets of Langerhans ; nitric oxide ; peroxynitrite ; superoxide
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract We have shown that nitric oxide treatment for 30–90 min causes inhibition of insulin secretion, DNA damage and disturbs sub-cellular organization in rat and human islets of Langerhans and HIT-T15 cells. Here rat islets and beta-cell lines were treated with various free radical generating systems S-nitrosoglutathione (nitric oxide), xanthine oxidase plus hypoxanthine (reactive oxygen species), 3-morpholinosydnonimine (nitric oxide, super-oxide, peroxynitrite, hydrogen peroxide) and peroxynitrite and their effects over 4 h to 3 days compared with those of the cytokine combination interleukin-1β, tumour necrosis factor-α and interferon-γ. End points examined were de novo protein synthesis, cellular reducing capacity, morphological changes and apoptosis by acridine orange cytochemistry, DNA gel electrophoresis and electron microscopy. Treatment (24–72 h) with nitric oxide, superoxide, peroxynitrite or combined cytokines differentially decreased redox function and inhibited protein synthesis in rat islets of Langerhans and in insulin-containing cell lines; cytokine effects were arginine and nitric oxide dependent. Peroxynitrite gave rare apoptosis in HIT-T15 cells and superoxide gave none in any cell type, but caused the most beta cell-specific damage in islets. S-nitroso-glutathione was the most effective agent at causing DNA laddering or chromatin margination characteristic of apoptotic cell death in insulin-containing cells. Cytokine-induced apoptosis was observed specifically in islet beta cells, combined cytokine effects on islet function and death most resembled those of the mixed radical donor SIN-1.
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  • 56
    ISSN: 1573-675X
    Keywords: Apoptosis ; cytokines ; macrophages ; nitric oxide
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract The immunological rejection of the AK-5 histiocytoma in syngeneic hosts involves the participation of NK cells and the upregulation of Th1 type cytokine response. The tumor cells are killed by necrosis and apoptosis. We have studied the role of host peritoneal macrophages in tumor regression. Activated macrophages from tumor- bearing animals produce cytokines like IL-1β, TNF-α, IL-12 and free radicals like nitric oxide during tumor regression. IL-12 and IFN-γ played a crucial role in the induction of NO production by the host macrophages, since administration of anti IL-12 and anti IFN-γ antibodies in AK-5 tumor-bearing animals suppressed NO production by the macrophages. Similarly the cytotoxic activity of the host macrophages which is dependent on NO production was also affected in antibody injected animals. These studies indicate an important role for cytokines in the activation of host macrophages which in turn produce nitric oxide that is involved in the induction of apoptosis in AK-5 cells, leading to the regression of the tumor.
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  • 57
    ISSN: 1573-675X
    Keywords: Apoptosis ; excitotoxicity ; glutamate ; cytoskeleton ; nitric oxide ; NMDA
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract The type of cell death encountered in neuronal cell cultures exposed to excitatory amino acids — such as glutamate, the major excitatory neurotransmitter in the central nervous system, or free radicals, such as nitric oxide (NO.) and superoxide anoin (O2. −), which react to form peroxynitrite (ONOO−) — appears to depend on the intensity of the exposure and may involve two temporarily distinct phases. Following relatively fulminant insults, an initial phase of necrosis — associated with extreme energy depletion — may simply reflect the failure of neurons to carry out the ‘default’ apoptotic death program used to efficiently dispose of aged or otherwise unwanted cells. Neurons recovering mitochondrial energy potential after an initial fulminant insult or following a more subtle inciting injury may subsequently undergo apoptosis, possibly associated with a factor released from mitochondria that triggers this death program. The maintenance of balanced energy production may be a decisive factor in detemining the degree, type, and progression of neuronal injury caused by ‘excitotoxins’ and free radicals. Similar events could possibly occur in vivo after ischemia or other insults.
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  • 58
    ISSN: 1573-515X
    Keywords: acidification ; anthropogenic nitrogen ; cations ; nitrate leaching ; nitric oxide ; nitrous oxide ; nutrient limitation ; phosphorus ; productivity ; tropical ecosystems
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Geosciences
    Notes: Abstract Human activities have more than doubled the inputs of nitrogen (N) into terrestrial systems globally. The sources and distribution of anthropogenic N, including N fertilization and N fixed during fossil fuel combustion, are rapidly shifting from the temperate zone to a more global distribution. The consequences of anthropogenic N deposition for ecosystem processes and N losses have been studied primarily in N-limited ecosystems in the temperate zone; there is reason to expect that tropical ecosystems, where plant growth is most often limited by some other resource, will respond differently to increasing deposition. In this paper, we assess the likely direct and indirect effects of increasing anthropogenic N inputs on tropical ecosytem processes. We conclude that anthropogenic inputs of N into tropical forests are unlikely to increase productivity and may even decrease it due to indirect effects on acidity and the availability of phosphorus and cations. We also suggest that the direct effects of anthropogenic N deposition on N cycling processes will lead to increased fluxes at the soilwater and soil-air interfaces, with little or no lag in response time. Finally, we discuss the uncertainties inherent in this analysis, and outline future research that is needed to address those uncertainties.
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  • 59
    ISSN: 1573-515X
    Keywords: ammonia emissions ; global nitrogen cycle ; nitric oxide ; nitrogen deposition ; nitrogen pollution
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Geosciences
    Notes: Abstract Increases and expansion of anthropogenic emissions of both oxidized nitrogen compounds, NOx, and a reduced nitrogen compound, NH3, have driven an increase in nitrogen deposition. We estimate global NOx and NH3 emissions and use a model of the global troposphere, MOGUNTIA, to examine the pre-industrial and contemporary quantities and spatial patterns of wet and dry NOy and NHx deposition. Pre-industrial wet plus dry NOx and NHx deposition was greatest for tropical ecosystems, related to soil emissions, biomass burning and lightning emissions. Contemporary NOy + NHx wet and dry deposition onto Northern Hemisphere (NH) temperate ecosystems averages more than four times that of pre-industrial N deposition and far exceeds contemporary tropical N deposition. All temperate and tropical biomes receive more N via deposition today than pre-industrially. Comparison of contemporary wet deposition model estimates to measurements of wet deposition reveal that modeled and measured wet deposition for both NO− 3 and NH+ 4 were quite similar over the U.S. Over Western Europe, the model tended to underestimate wet deposition of NO− 3 and NH+ 4 but bulk deposition measurements were comparable to modeled total deposition. For the U.S. and Western Europe, we also estimated N emission and deposition budgets. In the U.S., estimated emissions exceed interpolated total deposition by 3--6 Tg N, suggesting that substantial N is transported offshore and/or the remote and rural location of the sites may fail to capture the deposition of urban emissions. In Europe, by contrast, interpolated total N deposition balances estimated emissions within the uncertainty of each.
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  • 60
    ISSN: 1573-904X
    Keywords: FK409 ; isosorbide dinitrate ; nitric oxide ; L-cysteine ; antiplatelet activity
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Purpose. Recently, we have reported that FK409 spontaneously releases nitric oxide (NO) in solution. In the present study, the influence of L-cysteine (Cys) and glutathione (GSH), which are typical sulfhydryl group-bearing compounds, on NO release from FK409 and biological action of FK409 was examined. Methods. We evaluated the effects of Cys and GSH on NO release from FK409 by nitrite analysis or detection with a chemiiluminesence analyzer. In a biological study, the influence of Cys on inhibition of rat platelet aggregation of FK409 was investigated. In addition, the above mentioned characteristics of FK409 were compared with those of isosorbide dinitrate (ISDN). Results. FK409 decomposed spontaneously with generation of nitrite in solution. Both Cys and GSH accelerated decomposition of FK409 and nitrite generation from FK409 in a concentration-dependent manner. When the NO levels in the headspace of FK409 solutions (0.5 mM) reached equilibrium with and without 25 mM Cys, the constant rate for NO release from FK409 in the presence of Cys was 13 times larger than that in the absence of Cys. In biological study, FK409 (100 µM) showed 56 and 90% inhibition of rat platelet aggregation in the absence and presence of 10 mM Cys, respectively, whereas ISDN (100 µM) showed 10 and 23% inhibition, respectively. Conclusions. Decomposition of FK409 with generation of NO is spontaneous, and is accelerated in the presence of sulfhydryl group-bearing compounds, thereby potentiating the biological action of FK409.
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  • 61
    ISSN: 1573-904X
    Keywords: liposomes ; macrophages ; nitric oxide ; heat-stable macrophage priming factor
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Purpose. The effects of liposomes on nitric oxide (NO) production from mouse peritoneal macrophages following intraperitoneal injection of liposomes were investigated. Methods. Mouse peritoneal macrophages were collected following intraperitoneal injection of liposomes and cultured with and without lipopolysaccharide (LPS). Peritoneal washing fluid was also collected from the mice injected with liposomes. NO production was evaluated by measuring the concentration of nitrite in the macrophage culture supernatant by Griess reagent. Results. NO production stimulated by LPS was observed in peritoneal macrophages obtained from the liposome-treated mice, but liposomes did not activate macrophages directly to induce NO in response to LPS. NO production was higher in the liposomes composed of phospha-tidylcholine than that of negatively charged liposomes composed of phosphatidylserine. Peritoneal washing fluid obtained from mice injected with liposomes has a capacity to induce NO production in the macrophages from naive mice. This capacity was not diminished by heat-treatment at 100°C for 5 min. Conclusions. Peritoneal macrophages were activated to produce NO in response to LPS following intraperitoneal injection of liposomes. They did not activate macrophages directly, and the induction of heat-stable macrophage priming factor, but not cytokines, is suggested.
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  • 62
    ISSN: 1573-904X
    Keywords: nitrate tolerance ; nitric oxide ; cyclic GMP ; SIN-1 ; molsidomine ; glyceryl trinitrate
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Purpose. Using an established cell culture model, the present study investigates whether linsidomine (SIN-1), a spontaneous donor of nitric oxide and active metabolite of the antianginal drug molsidomine, induces tolerance to its own cyclic GMP stimulatory action or shows a diminished response after tolerance induction with glyceryl trinitrate. Methods. Incubations with nitric oxide donors were carried out in LLC-PK1, kidney epithelial cells. Intracellular levels of cyclic GMP, the vasodilatory second messenger of nitric oxide, were determined by radioimmunoassay. Results. A 5-h preincubation with glyceryl trinitrate (0.01−100 μM) led to complete inhibition of a subsequent cyclic GMP stimulation by glyceryl trinitrate but left the cyclic GMP response to SIN-1 unaltered. Similarly, cyclic GMP elevations by the spontaneous nitric oxide donors sodium nitroprusside and spermine NONOate were not affected after pretreatment with glyceryl trinitrate. Moreover, pretreatment with SIN-1 (1−1000 μM) had no significant effect on SIN-1-dependent cyclic GMP stimulation. Conclusions. Our results show that in LLC-PK1, cells, SIN-1 is free of tolerance induction and not cross-tolerant to glyceryl trinitrate. This may be due to the spontaneous nitric oxide release from SIN-1, which in contrast to nitric acid esters does not require enzymatic bioactivation and may therefore be unaffected by nitrate tolerance.
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  • 63
    ISSN: 1573-904X
    Keywords: FK409 ; nitric oxide ; L-cysteine ; glutathione
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Purpose. We have recently reported that degradation of FK409 with generation of NO is spontaneous and is accelerated in the presence of sulfhydryl-bearing compounds, such as L-cysteine (Cys) and glutathione (GSH). The purpose of the present study is to investigate the NO-releasing pathway of FK409 in the presence of sulfhydryl-bearing compounds. Methods. The degradation process of FK409 in the presence of Cys or GSH was investigated by means of 1H-nuclear magnetic resonance (NMR) spectroscopy and high-performance liquid chromatography (HPLC). Results. The degradation of FK409 in the presence of Cys was dependent on concentration of Cys, and showed pH-dependency, accelerating with an increase in pH. The 1H-NMR spectra of FK409 with Cys suggested that time-dependent elimination of the hydrogen atom at the α-position of the nitro moiety (5-position) was accelerated by Cys in weakly alkaline solution. Cys and GSH were transformed readily, concomitant with FK409 degradation, to give their oxidized forms and probably S-nitrosothiols. Conclusions. The effect of sulfhydryl-bearing compounds on FK409 degradation is due to the acceleration of deprotonation of the hydrogen atom at the 5-position by thiolate anion as well as hydroxyl ion. Sulfhydryl-bearing compounds reacted with the released NO resulting in formation of disulfides via intermediate S-nitrosothiols.
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  • 64
    ISSN: 1573-904X
    Keywords: nitric oxide ; NO ; benzofuroxans ; NO donors
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Purpose. To investigate the effect of benzofusion on NO donor properties and related biological activities of the furoxan system. The biological properties considered were the ability to increase the cytosolic levels of cGMP in C6 cells and vasodilation. Methods. NO donor properties were investigated either in the presence or the absence of cysteine by using the Griess reaction, chemiluminescence, and gas chromatography. Increase of cytosolic cGMP levels were evaluated by radioimmunoassay. Vasodilating activity was assessed on rat aorta strips precontracted with noradrenaline, in the presence and the absence of oxyhemoglobin (HbO2) and methylene blue (MB), respectively. Results. Benzofuroxan and its methyl and cyano derivatives were unable to release NO under the experimental conditions. Generally these compounds displayed feeble vasodilating properties and were able to weakly stimulate soluble guanylate cyclase (sGC). By contrast, benzodifuroxan and benzotrifuroxan were able to produce both NO• and its reduced form NO−, the nitroxyl anion. They displayed potent vasodilating properties and were able to increase cytosolic levels of cGMP in a concentration-dependent manner. Conclusions. The simple benzofuroxans considered here are devoid of the capability to release NO, they weakly stimulate sGC as well as manifest feeble vasodilating properties by a mechanism that does not involve a thiol-induced NO production. By contrast, benzodifuroxan and benzotrifuroxan behave as typical NO donor furoxans.
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  • 65
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    Pharmaceutical research 13 (1996), S. 649-662 
    ISSN: 1573-904X
    Keywords: oxygen radical ; nitric oxide ; peroxynitrite ; oxidative stress ; vascular system ; reactive nitrogen species
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Free radicals, such as superoxide, hydroxyl and nitric oxide, and other “reactive species”, such as hydrogen peroxide, hypochlorous acid and peroxynitrite, are formed in vivo. Some of these molecules, e.g. superoxide and nitric oxide, can be physiologically useful, but they can also cause damage under certain circumstances. Excess production of reactive oxygen or nitrogen species (ROS, RNS), their production in inappropriate relative amounts (especially superoxide and NO ) or deficiencies in antioxidant defences may result in pathological stress to cells and tissues. This oxidative stress can have multiple effects. It can induce defence systems, and render tissues more resistant to subsequent insult. If oxidative stress is excessive or if defence and repair responses are inadequate, cell injury can be caused by such mechanisms as oxidative damage to essential proteins, lipid peroxidation, DNA strand breakage and base modification, and rises in the concentration of intracellular “free” Ca2+. Considerable evidence supports the view that oxidative damage involving both ROS and RNS is an important contributor to the development of atherosclerosis. Peroxynitrite (derived by reaction of superoxide with nitric oxide) and transition metal ions (perhaps released by injury to the vessel wall) may contribute to lipid peroxidation in atherosclerotic lesions.
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  • 66
    ISSN: 1573-515X
    Keywords: drainage ; denitrification ; methane ; nitric oxide ; nitrous oxide ; nitrification
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Geosciences
    Notes: Abstract Intermittent drainage of rice fields isdiscussed as an option to mitigate emission ofCH4, an important greenhouse gas. HoweverN2O, a potentially more effective greenhouse gas,may be emitted during the aeration phase. Therefore,the metabolism of NO, N2O, NH $$_4^ + $$ ,NO $$_2^ - $$ and NO $$_3^ - $$ and the kinetics ofCH4 oxidation were measured after aeration ofmethanogenic rice field soil. Before aeration, thesoil contained NH $$_4^ + $$ in relatively highconcentrations (about 4 mM), while NO $$_2^ - $$ andNO $$_3^ - $$ were almost undetectable. Immediatelyafter aeration both NO and N2O were produced withrates of about 15 pmol h-1 gdw-1 and 5 pmolh-1 gdw-1, respectively. Simultaneously,NH $$_4^ + $$ decreased while NO $$_2^ - $$ accumulated. Later on, NO $$_2^ - $$ was depletedwhile NO $$_3^ - $$ concentrations increased.Characteristic phases of nitrogen turnover wereassociated with the activities of ammonium oxidizers,nitrite oxidizers and denitrifiers. Oxidation ofNH $$_4^ + $$ and production of NO and N2O wereinhibited by 10 Pa acetylene demonstrating thatnitrification was obligatory for the initiation ofnitrogen turnover and production of NO and N2O.Ammonium oxidation was not limited by the availableNH $$_4^ + $$ and thus, concomittant production of NOand N2O was not stimulated by addition ofNH $$_4^ + $$ . However, addition of NO $$_3^ - $$ stimulated production of NO and N2O in bothanoxic and aerated rice soil slurries. In this case,10 Pa acetylene did not inhibit the production of NOand N2O demonstrating that it was due todenitrification which was obviously limited by theavailability of NO $$_3^ - $$ . In the aerated soilslurries CH4 was only oxidized if present atelevated concentrations 〉50 ppmv CH4). Atatmospheric CH4 concentrations (∼1.7 ppmv)CH4 was not consumed, but was even slightly produced.CH4 oxidation activity increased afterpreincubation at 20% CH4, and then CH4was also oxidized at atmospheric concentrations. CH4oxidation kinetics exhibited sigmoid characteristicsat low CH4 concentrations presumably because ofinhibition of CH4 oxidation by NH $$_4^ + $$ .
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  • 67
    ISSN: 1573-515X
    Keywords: ammonia emissions ; global nitrogen cycle ; nitric oxide ; nitrogen deposition ; nitrogen pollution
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Geosciences
    Notes: Abstract Increases and expansion of anthropogenic emissions of both oxidized nitrogen compounds, NOx, and a reduced nitrogen compound, NH3, have driven an increase in nitrogen deposition. We estimate global NOx and NH3 emissions and use a model of the global troposphere, MOGUNTIA, to examine the pre-industrial and contemporary quantities and spatial patterns of wet and dry NOy and NHx deposition. Pre-industrial wet plus dry NOx and NHx deposition was greatest for tropical ecosystems, related to soil emissions, biomass burning and lightning emissions. Contemporary NOy+NHx wet and dry deposition onto Northern Hemisphere (NH) temperate ecosystems averages more than four times that of preindustrial N deposition and far exceeds contemporary tropical N deposition. All temperate and tropical biomes receive more N via deposition today than pre-industrially. Comparison of contemporary wet deposition model estimates to measurements of wet deposition reveal that modeled and measured wet deposition for both NO 3 − and NH 4 + were quite similar over the U.S. Over Western Europe, the model tended to underestimate wet deposition of NO 3 − and NH 4 + but bulk deposition measurements were comparable to modeled total deposition. For the U.S. and Western Europe, we also estimated N emission and deposition budgets. In the U.S., estimated emissions exceed interpolated total deposition by 3-6 Tg N, suggesting that substantial N is transported offshore and/or the remote and rural location of the sites may fail to capture the deposition of urban emissions. In Europe, by contrast, interpolated total N deposition balances estimated emissions within the uncertainty of each.
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  • 68
    ISSN: 1573-515X
    Keywords: acidification ; anthropogenic nitrogen ; cations ; nitrate leaching ; nitric oxide ; nitrous oxide ; nutrient limitation ; phosphorus ; productivity ; tropical ecosystems
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Geosciences
    Notes: Abstract Human activities have more than doubled the inputs of nitrogen (N) into terrestrial systems globally. The sources and distribution of anthropogenic N, including N fertilization and N fixed during fossil fuel combustion, are rapidly shifting from the temperate zone to a more global distribution. The consequences of anthropogenic N deposition for ecosystem processes and N losses have been studied primarily in N-limited ecosystems in the temperate zone; there is reason to expect that tropical ecosystems, where plant growth is most often limited by some other resource, will respond differently to increasing deposition. In this paper, we assess the likely direct and indirect effects of increasing anthropogenic N inputs on tropical ecosytem processes. We conclude that anthropogenic inputs of N into tropical forests are unlikely to increase productivity and may even decrease it due to indirect effects on acidity and the availability of phosphorus and cations. We also suggest that the direct effects of anthropogenic N deposition on N cycling processes will lead to increased fluxes at the soil-water and soil-air interfaces, with little or no lag in response time. Finally, we discuss the uncertainties inherent in this analysis, and outline future research that is needed to address those uncertainties.
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  • 69
    ISSN: 1573-6881
    Keywords: Cytochrome c oxidase ; nitric oxide ; copper ; inhibition ; respiration ; mechanism
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology , Physics
    Notes: Abstract Nitric oxide (NO) has recently been recognized as an important biological mediator that inhibits respiration at cytochrome c oxidase (CcO). This inhibition is reversible and shows competition with oxygen, the K i being lower at low oxygen concentrations. Although the species that binds NO in turnover has been suggested to contain a partially reduced binuclear center, the exact mechanism of the inhibition is not clear. Recently, rapid (ms) redox reactions of NO with the binuclear center have been reported, e.g., the ejection of an electron to cytochrome a and the depletion of the intermediates P and F. These observations have been rationalized within a scheme in which NO reacts with oxidized CuB leading to the reduction of this metal center and formation of nitrite in a very fast reaction. Electron migration from CuB to other redox sites within the enzyme is proposed to explain the optical transitions observed. The relevance of these reactions to the inhibition of CcO and metabolism of NO are discussed.
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  • 70
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    Cell biology and toxicology 12 (1996), S. 271-274 
    ISSN: 1573-6822
    Keywords: vascular smooth-muscle cells ; vasoactive peptides ; neutral endopeptidase ; nitric oxide
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract Various in vitro preparations have been utilized to study the cellular activity of vasoactive agents on renal cortical microvessels and on mesangial cells. The receptors and the transduction pathways of bradykinin and atrial natriuretic factor were characterized on cultured cortical vascular smooth muscle cells from the rabbit kidney. A preparation of afferent arterioles that had been freshly isolated from the rat kidney was used to study the NO-dependent regulation of renin release. The influence of endothelin and angiotensin II on mesangial cell proliferation was evaluated, using cocultures of human endothelial and mesangial cells. These appropriate in vitro preparations have provided new insights on renal vascular endocrinology. However, extrapolation of in vitro data to in vivo physiology must be cautious because the phenotype of vascular cells often changes in culture conditions.
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  • 71
    ISSN: 1573-2614
    Keywords: nitric oxide ; high frequency oscillatory ventilation ; chemiluminescence assay ; electrochemical assay ; mechanical ventilation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Computer Science , Medicine
    Notes: Abstract Objective. The objective of this study is to determine the accuracy andprecision of chemiluminescence and electrochemical nitric oxide (NO)measurements and accuracy of NO dosage with electronic mass flow controllers(MFC) versus rotameters during NO inhalational therapy. Methods. NO flow wasdelivered to a high frequency oscillator and mixed with ventilator flow. NOand NO2 concentrations were measured simultaneously with astandard chemiluminescence analyzer and a modified electrochemical analyzer.Dosage accuracy was assessed with gas flows adjusted with either MFC’sor rotameters. Accuracy of both analyzers was validated with both NO andventilator flow regulated with a MFC. Results. In dry air, without pulsatilepressure, MFC controlled NO and ventilator flow resulted in an accuracyexpressed as the ratio of calculated concentration to measured concentration(RCM) of 0.995 (CI: 0.983–0.988) when measured with chemiluminescence.When the ventilator rotameter was used instead of a MFC, RCM was 0.856 (CI:0.835–0.877). With a rotameter for both NO and ventilator flow, RCMincreased to 1.175 (CI: 0.793–1.740) with an increase of confidenceinterval limits. Chemiluminescence was sensitive to humidification of theventilatory gases (p 〈 0.05), slightly sensitive to the addition ofoxygen and to pulsatile pressure (not significant). RCM obtained with themodified electrochemical analyzer was in close agreement withchemiluminescence RCM, although 95% CI were wider withelectrochemical analysis. Conclusions. During high frequency oscillatoryventilation (HFOV), standard rotameter flow control of both NO andventilator flow results in unpredictable NO concentrations that would beclinically unacceptable. When one MFC was used for NO flow control, withventilator flow controlled with a rotameter, this resulted in moderatedosage accuracy. To achieve a still higher accuracy, MFC flow control forboth NO and ventilator flow is indicated. During HFOV, standardchemiluminescence analyzers cannot be considered to be the gold standard fordetermination of the NO concentration delivered. Measurement of NOconcentration may not be mandatory for determination of inhaled NO doseduring HFOV, but may be used to monitor for unsafe or unwanted events.
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  • 72
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    Journal of atmospheric chemistry 27 (1997), S. 249-269 
    ISSN: 1573-0662
    Keywords: atmospheric surface layer ; constant-flux layer ; ozone ; nitric oxide ; radon ; thoron ; thoron exhalation ; Damköhler ratio ; eddy diffusivity
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Geosciences
    Notes: Abstract We have discussed the behavior of a non-conserved scalar in the stationary, horizontally homogeneous, neutral surface-flux layer and, on the basis of conventional second-order closure, derived analytic expressions for flux and for mean concentration of a gas, subjected to a first-order removal process. The analytic flux solution showed a clear deviation from the constant flux, characterizing a conserved scalar in the surface-flux layer. It decreases with height and is reduced by an order of magnitude of the surface flux at a height equal to about the typical mean distance a molecule can travel before destruction. The predicted mean concentration profile, however, shows only a small deviation from the logarithmic behavior of a conserved scalar. The solution is consistent with assuming a flux-gradient relationship with a turbulent diffusivity corrected by the Damköhler ratio, the ratio of a characteristic turbulent time scale and the scalar mean lifetime. We show that if we use only first-order closure and neglect the effect of the Damköhler ratio on the turbulent diffusivity we obtain another analytic solution for the profiles of the flux and the mean concentration which, from an experimental point of view, is indistinguishable from the first analytic solution. We have discussed two cases where the model should apply, namely NO which, by night, is irreversibly destroyed by interaction with mainly O3 and the radioactive 220Rn. Only in the last case was it possible to find data to shed light on the validity of our predictions. The agreement seemed such that a falsification of our model was impossible. It is shown how the model can be used to predict the surface flux of 220Rn from measured concentration profiles.
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  • 73
    ISSN: 1573-515X
    Keywords: C3 and C4 plant functional types ; grasslands ; methane oxidation ; nitric oxide ; nitrous oxide
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Geosciences
    Notes: Abstract Plant community structure is expected to regulate the microbial processes of nitrification and denitrification by controlling the availability of inorganic N substrates. Thus it could also be a factor in the concomitant release of NO and N2O from soils as a result of these processes. C3 and C4 plants differ in several attributes related to the cycling of nitrogen and were hypothesized to yield differences in trace gas exchange between soil and atmosphere. In this study we estimated fluxes of NO, N2O and CH4 from soils of shortgrass steppe communities dominated by either C3 plants, C4 plants or mixtures of the two types. We collected gas samples weekly from two sites, a sandy clay loam and a clay, throughout the growing seasons of 1995 and 1996. Plant functional type effects on gas fluxes at the clay site were not apparent, however we found several differences among plant communities on the sandy clay loam. CH4 uptake from atmosphere to soil was significantly greater on C4 plots than C3 plots in both years. NO fluxes were significantly greater from C4 plots than from C3 plots in 1995. NO fluxes from C3 and mixed plots were not significantly different between 1995 and 1996, however fluxes from C4 plots were significantly greater in 1995 compared to 1996. Results indicate that under certain environmental conditions, particularly when factors such as moisture and temperature are not limiting, plant community composition can play an important role in regulating trace gas exchange.
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  • 74
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    Reaction kinetics and catalysis letters 58 (1996), S. 73-78 
    ISSN: 1588-2837
    Keywords: Reduction ; nitric oxide ; dinitrogen ; carbon monoxide ; dioxygen ; copper-manganese oxide ; spinel
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The activity of γ−Al2O3-supported CuxMn3-xO4 catalysts towards the reduction of NO with CO has been investigated at temperatures of 150–500°C. It was established that the most active sample is Cu1.01Mn1.99O4/γ−Al2O3,i.e. the sample where the CuMn2O4 spinel is formed. In the presence of oxygen and the reducing agents CO and HC (a propane-butane mixture) oxygen has no blocking effect on the NO+CO reaction. Under oxidative conditions the reactions NO+CO and O2+CO are competitive.
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  • 75
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    Reaction kinetics and catalysis letters 65 (1998), S. 139-144 
    ISSN: 1588-2837
    Keywords: silver ; silver sulfate ; nitric oxide ; catalytic reduction
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The influence of SO2 (200 ppm) on the durability of a Ag/Al2O3 catalyst for the reduction of NOx with ethyl alcohol was examined. The results strongly suggest that H2O in diesel engine exhaust is essential for the high durability of Ag/Al2O3 catalyst in the presence of SO2.
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  • 76
    ISSN: 1573-904X
    Keywords: microcirculation ; vasomotor tone ; amphipathic pep-tides ; nitric oxide ; PEG-DSPE micelles
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Purpose. To determine whether human vasoactive intestinal peptide (VlP)-poly(ethylene glycol) (PEG)-grafted distearoyl-phosphatidyleth-anolamine (DSPE) micelles elicit potent and stable vasodilation in vivo. Methods. PEG-DSPE micelles were prepared by co-precipitation. VIP was loaded into micelles by incubation at room temperature. Vasoactivity of VIP in SSM was determined by monitoring changes in diameter of resistance arterioles in the in situ hamster cheek pouch using intravital microscopy. Results. VIP easily undergoes self-assembly into small PEG-DSPE micelles (mean [±SEM] size, 18 ± 1 nm) in a time-dependent fashion. This generates a potent vasoactive matrix at nanomole concentrations of VIP as manifested by ~3-fold potentiation and prolongation of vasodilation relative to that evoked by aqueous VIP alone (p 〈 0.05). This response is specific and mediated by the L-arginine/nitric oxide (NO) biosynthetic pathway. Micellar VIP dispersion remains vasoactive for at least 14 days after preparation and storage at 4°C. Conclusions. A novel, self-associated, small and stable PEG-DSPE micellar formulation of VIP amplifies vasodilation in the in situ peripheral microcirculation in a specific fashion by elaborating NO. An optimized formulation could be considered for certain cardiovascular disorders associated with L-arginine/NO biosynthetic pathway dysfunction.
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  • 77
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    Pharmaceutical research 15 (1998), S. 870-876 
    ISSN: 1573-904X
    Keywords: rectal mucosa ; absorption enhancer ; nitric oxide
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Purpose. The objective of this investigation is to evaluate the potential of nitric oxide (NO) donors as a new class of absorption enhancers which may act on intestinal epithelial cells through epithelial actions of the chemical mediator, NO. Methods. Suppositories containing NO donors and insulin were administered into the rabbit rectum. After administration of the suppository, blood samples were collected from the auricular vein. The plasma insulin and glucose concentrations were determined. Results. The NO donor S-nitroso-N-acetyl-DL-penicillamine (SNAP, 4 mg) induced a significant increase in the rate of insulin absorption from the rectum. Administration of a suppository containing SNAP without insulin affected neither the plasma insulin nor the plasma glucose concentration. Other NO donors, NOR1 and NOR4, also induced increases in the insulin absorption. The absorption enhancement effect of SNAP was inhibited by coadministration of the NO scavenger carboxy-PTIO. SNAP also enhanced FITC-dextran (MW 4,000) absorption. Little cytotoxicity of SNAP (3.0 mg/ml) as assessed in terms of the rate of lactate dehydrogenase (LDH) release from Caco-2 cells was detected for 2 h of incubation. Conclusions. These findings suggest that NO enhanced macromolecular absorption from the rectum without mucosal cell damage, and that NO donors can act as potent absorption enhancers.
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  • 78
    ISSN: 1573-8221
    Keywords: adaptation to hypoxia ; nitric oxide ; endothelial relaxation factor ; endothelium-dependent relaxation ; tail artery
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract Adaptation to intermittent hypoxic hypoxia did not affect the endothelium-dependent relaxation of the aorta in rats, but significantly increased the relaxation of their tail artery. Following the adaptation, the NO level fell in the liver, intestine, and kidneys and remained unchanged in the spleen. Adaptation to hypoxia presumably limits NO synthesis and/or release in the vascular endothelium or enhances the capacity of this oxide to bind in a physiologically active depot.
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  • 79
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    Bulletin of experimental biology and medicine 126 (1998), S. 829-834 
    ISSN: 1573-8221
    Keywords: nitric oxide ; wound healing ; microcirculation ; inflammation ; aerial plasma
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract Pronounced wound-healing effect of exogenous nitric oxide obtained by the plasma chemical method was confirmed in rats with aseptic and infected wounds and in patients with complicated stubborn wounds, postradiation and trophic ulcers, necroses of transplanted skin flaps, etc. Morphological study revealed normalization of microcirculation, decreased inflammation, enhanced phagocytosis, activation of macrophages, and accelerated proliferation of fibroblasts.
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  • 80
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    Bulletin of experimental biology and medicine 121 (1996), S. 377-379 
    ISSN: 1573-8221
    Keywords: nitric oxide ; NO-synthetase ; CCl 4 ; antioxidants
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    Topics: Biology , Medicine
    Notes: Abstract The effect of CCl4 on the generation of NO in mouse liver cells is studiedin vivo. Injection of CCl4 is shown to modulate the synthesis of NO by activating the NO-synthetase system. The experimental data suggest that O2 − plays an essential role in the regulation of NO-synthetase system.
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  • 81
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    Bulletin of experimental biology and medicine 121 (1996), S. 388-391 
    ISSN: 1573-8221
    Keywords: nitric oxide ; cyclic 3′,5′-guanosine monophosphate, desensitization of choline receptors ; snail neurons
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract Desensitization of choline receptors is studied after pharmacological effects on the intracellular level of nitric oxide and cyclic guanosine monophosphate in snail neurons. It is shown that inhibitors of NO synthase do not alter desensitization, whereas an activator of guanylate cyclase as well as intracellular injection of guanosine monophosphate boost it.
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  • 82
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    Bulletin of experimental biology and medicine 121 (1996), S. 471-474 
    ISSN: 1573-8221
    Keywords: nitric oxide ; heat shock ; electron paramagnetic resonance ; inhibitor of NO synthase
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    Topics: Biology , Medicine
    Notes: Abstract Heat shock is shown to lend a marked boost to the production of nitric oxide (NO), which attains the maximal level 1 hour after exposure and returns to the initial level after 24 hours. The generation of NO in all studied organs is completely blocked by Nω-nitro-L-arginine, an inhibitor of NO synthase, both in the control and after hyperthermia. Thus, heat shock markedly stimulates NO synthesis. This generalized effect may underlie the drop in the peripheral vascular tone that is characteristic of heat shock.
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  • 83
    ISSN: 1573-8221
    Keywords: nitric oxide ; heat shock ; Wistar rats ; August rats
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    Topics: Biology , Medicine
    Notes: Abstract The content of NO in the kidneys, heart, and spleen of intact August rats surpasses that of Wistar rats. After heat shock the content of NO rises: in the kidneys 15.5-fold, in the liver 3.2-fold, in the heart 10-fold, in the spleen 6.4-fold, in the intestine 2.8-fold, and in the brain 1.9-fold. Thus, August rats, which are less resistant to heat shock than Wistar rats, are characterized by a more pronounced activation of NO synthesis in response to heat shock.
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  • 84
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    Bulletin of experimental biology and medicine 124 (1997), S. 955-958 
    ISSN: 1573-8221
    Keywords: nitric oxide ; adaptation ; heat shock ; endothelium-dependent relaxation ; blood pressure
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract Adaptation to stress reduces animal mortality in heat stress from 57 to 8% and prevents a decrease in blood pressure as well as excessive inhibition of constrictory and potentiation of dilatory reactions of isolated aorta associated with hyperproduction of NO. It is assumed that beneficial effect of adaptation is due to accumulation of a reserve pool of NO, which either has a direct effect, or mediates activation or synthesis of another protective factor.
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  • 85
    ISSN: 1573-8221
    Keywords: adaptation ; nitric oxide ; NO donor ; NO synthetase inhibitor ; stress ; gastric ulcer ; protection
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract The iron dinitrosyl complex (a NO donor), adaptation to stress, and their combination suppress the stress-induced ulcer formation. Nω-nitro-L-arginine, a NO synthetase inhibitor, reduce the antistress effect of adaptation. Severe stress induces a sharp decrease in the NO production in the liver and brain. After adaptation to stress, the NO production in the liver and brain does not differ significantly from control levels. However, adaptation attenuates a decrease in the NO production in the liver caused by severe stress.
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    Bulletin of experimental biology and medicine 128 (1999), S. 803-805 
    ISSN: 1573-8221
    Keywords: ischemia ; reperfusion ; microcirculation ; distant disturbances ; nitric oxide
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract Responsiveness, thrombogenicity, and thromboresistance of mesenteric microvessels were studied in rats during postischemic reperfusion of the intestine, brain, and hind limb. Irrespective to localization of the ischemized organ, the mesenteric microvessels increased responsiveness and decreased thromboresistance. Vascular thrombogenicity depended on the localization of ischemia. During cerebral reperfusion, thrombogenicity of some venules was decreased against the background of its general increase in arterioles. Microvascular disturbances and predominantly related to perturbations in nitric oxide synthesis.
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  • 87
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    Bulletin of experimental biology and medicine 128 (1999), S. 782-785 
    ISSN: 1573-8221
    Keywords: synapse ; nitric oxide ; nerve terminal ionic currents ; transmitter secretion
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract Extracellular recording was used to study the effect of sodium nitroprusside, a donor of NO, on endplate transmitter release and ionic currents in frog cutaneous pectoris muscle. Exogenous NO inhibits induced transmiter secretion, and this effect is antagonized by extracellular Ca2+. Exogenous NO increases potential-dependent outward potassium current and inhibits Ca2+-activated potassium current in the motor nerve terminals.
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  • 88
    ISSN: 1573-8221
    Keywords: nitric oxide ; Ca2+-ATPase ; expression ; reperfusion ; physical exercise
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract This study verifies the hypothesis that NO-dependent regulation of sarcoplasmic reticulum Ca2+-ATPase gene (SERCA) plays an important role in preventing Ca2+ overload after exposure to damaging factors. The data confirmed NO-dependent activation of SERCA expression and important role of this mechanism in the reduction of calcium overload.
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  • 89
    ISSN: 1573-8221
    Keywords: nitric oxide ; heat-shock proteins ; hypotension ; adaptation
    Source: Springer Online Journal Archives 1860-2000
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    Notes: Abstract The role of HSP70 and nitric oxide in antihypotensive effects of thermal adaptation was studied. Western blot analysis and electron paramagnetic resonance were used to determine the contents of HSP70 and nitric oxide. Protective effect of adaptation was evaluated by the limitation of blood pressure drop after heat shock. The formation of protective effects, accumulation of HSP70, and development of the ability to decrease nitric oxide overproduction had similar dynamic patterns and appeared at the same period. Quercetin, an inhibitor of HSP70 synthesis, prevented the development of protective effects. The data suggest that HSP70 accumulated during adaptation prevents heat shock-induced hypotension by restricting NO over-production and interfering with its cytotoxic effects.
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  • 90
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    Bulletin of experimental biology and medicine 124 (1997), S. 968-970 
    ISSN: 1573-8221
    Keywords: nitric oxide ; nephrotoxicity ; radiopaque agents ; verapamil
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract Nephrotoxicity of radiopaque agents and the role of nitric oxide in its realization are studied in Wistar rats with Verograffin-induced acute renal insufficiency. Experiments demonstrate a significant decrease in nitric oxide production in the kidneys due to inhibition of constitutive NO-synthetase and disturbances of renal function, hemodynamics, and electrolyte balance. These changes are prevented by simultaneous injection of verapamil.
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  • 91
    ISSN: 1573-8221
    Keywords: hemoglobin oxygen affinity ; lipid peroxidation ; lipopolysaccharide ; nitric oxide
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract Effects of correction of the L-arginine—NO pathway on the fever reaction, oxygen transport function of the blood, and prooxidant-antioxidant equilibrium in rats injected intramuscularly with lipopolysaccharide were studied. pH, Pco2, Po2, and the index of hemoglobin oxygen affinity (p50) were measured in mixed venous blood. Levels of Schiff bases, α-tocopherol, and catalase activity were determined in erythrocytes and in the liver, kidneys, and heart. NO synthase inhibitor attenuated the fever reaction and decreased p50 to 28.89±0.83 mm Hg (in rats administered with lipopolysaccharide, p50 was 34.21±1.63 mm Hg). The increase in the content of Schiff bases and the exhaustion of the antioxidant system in erythrocytes and tissues were less pronounced in rats injected with the NO synthase inhibitor than in animals receiving lipopolysaccharide only. Various parameters of the prooxidant-antioxidant equilibrium correlated with p50. Thus, hemoglobin oxygen affinity and NO are important factors involved in the maintenance of the prooxidant-antioxidant equilibrium in the body.
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  • 92
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    Bulletin of experimental biology and medicine 126 (1998), S. 1177-1183 
    ISSN: 1573-8221
    Keywords: heat-shock proteins ; preconditioned and adaptive cardioprotection ; nitric oxide ; myocardial infarction
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract Here we summarized the results of our studies and the data on the role and protective effects of heat-shock proteins, mechanisms of activation of their synthesis, and the role of nitric oxide in this process. The role of heat-shock proteins in preconditioned and adaptive cardioprotection and the possibility of their use as prognostic criteria in cardiology are discussed
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  • 93
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    Bulletin of experimental biology and medicine 128 (1999), S. 867-869 
    ISSN: 1573-8221
    Keywords: nitric oxide synthase ; nitric oxide ; chromaffinocytes ; exocytosis
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract We examined NADPH-diaphorase co-localized with nitric oxide synthase in chromaffin cells of microparaganglia of rat respiratory organs. Nitric oxidergic function of chromaffinocytes and participation of nitric oxide in exocytosis of biogenic monoamines are established.
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  • 94
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    Bulletin of experimental biology and medicine 120 (1995), S. 691-694 
    ISSN: 1573-8221
    Keywords: nitric oxide ; L-glutamate receptor ; granule cells ; cerebellum
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract Stimulation of L-glutamate receptors (GluRs) is thought to produce neuron death through the elevation of free intracellular Ca2+ levels, leading to activation of Ca2+/calmodulin-dependent synthesis of cytotoxic amounts of NO·. In the present study, NO synthase activation mediated by mGluR stimulation is investigated in primary cultures of granule cells (CGrC). It is found that a selective agonist of mGluRs, DL-1-aminocyclopentane-trans-1,3-dicarboxylic acid (ACPD), raises both the cGMP and nitrite (NO2 −) levels, which are used as a biochemical index to study the enzymatic NO· release from L-arginine. This effect is abolished by applying both Nω-nitro-L-arginine methyl ester (NAME) and DL-2-amino-4-phosphonobytyric acid (AP4), and is independent of Ca2+. In contrast, the α-amino-3-hydroxy-5-methylisoxarole-4-propionnate (AMPA)-induced increase in cGMP content is eliminated by the preincubation of CGrC with 4 mM EGTA-chelated Ca2+.
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  • 95
    ISSN: 1573-8221
    Keywords: nitric oxide ; NO synthase ; brain ; individual behavior
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract NO synthase activity and the generation of reactive oxygen species (ROS) were measured in different brain regions of old rats separated in an “emotional resonance” test into two groups: passive rats (those preferring a dark space) and active ones (those preferring a lighted space). In both groups, NO synthase activity and ROS generation were at the highest level in the cerebellum. In the tested brain regions of active rats, NO synthase activity was lower and ROS generation more strongly marked than in the respective regions of passive rats. Interregional positive linear correlations were discovered both for NO synthase activity and for ROS generation. When the two groups were considered together, negative correlations were detected between NO synthase activity and ROS generation.
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  • 96
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    Bulletin of experimental biology and medicine 120 (1995), S. 792-795 
    ISSN: 1573-8221
    Keywords: nitric oxide ; NO synthase ; NADPH ; brain
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract A novel approach to the measurement of NO synthase activity in brain tissue is described. In the NO synthase-catalyzed reaction, NADPH undergoes stoichiometric oxidation and, using a known specific inhibitor of this oxidation, NO synthase activity can be estimated by recording the oxidation rate. In the proposed approach, NADPH oxidation is recorded fluorimetrically, and the rate of this reaction in the presence of Nω-nitro-L-arginine is subtracted from its initial rate in the presence of L-arginine. This approach can be used to develop a simple, sensitive, and specific method for estimating NO synthase activity in brain structures of small animals.
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  • 97
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    Bulletin of experimental biology and medicine 123 (1997), S. 419-423 
    ISSN: 1573-8221
    Keywords: nitric oxide ; NO-synthase ; cerebral ischemia ; convulsions
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract Nitric oxide is a gaseous chemical meassenger involved in the regulation of respiration, cardiovascular homeostasis, immunity, macrophagal activity, gene expression, morphogenesis, synaptic plasticity of the nervous tissue, memory, and release of neurotransmitters. This compound acts as a pathological factor in the states associated with neurodegeneration, ischemia, stroke and convulsions.
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  • 98
    ISSN: 1573-8221
    Keywords: natural suppressor cells ; nitric oxide ; leukemia ; granulocyte-macrophage precursors
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract In 4-month-old leukemia-prone AKR mice, the ability of bone marrow cells to inhibit proliferation of concanavalin A-stimulated splenocytes and mastocytoma P815 cellsin vitro was sharply increased in the preleukemic period. In 7-month-old mice, differences in natural suppressive activity of bone marrow cells were significant, but less pronounced than in 4-month-old mice. The immunosuppressive activity was not found in the spleen. In 4-month-old AKR mice, in the inhibition of proliferation of mitogen-stimulated splenocytes was increased due to enhanced NO production by bone marrow cells. These findings suggest that the increased antiproliferative activity observed in the bone marrow of AKR mice long before the appearance of clinical manifestations of leukemia is associated with disturbances in differentiation of myeloid progenitor cells and accumulation of natural suppressor cells in the bone marrow.
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  • 99
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    Bulletin of experimental biology and medicine 127 (1999), S. 460-462 
    ISSN: 1573-8221
    Keywords: ventricular arrhythmias ; nitric oxide ; NO-synthase inhibitor
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract On the model of occlusion/reperfusion arrhythmia in cats it was shown that repeated injections of the NO-synthase inhibitor L-NAME decreased the incidence of occlusion arrhythmias (to 40%), eliminated reperfusion-induced ventricular fibrillation, and drastically reduced the latency of occlusion arrhythmias. A single injection of L-NAME (20 mg/kg) immediately before ligation of the coronary artery did not decrease the incidence of occlusion and reperfusion arrhythmias.
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  • 100
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    Bulletin of experimental biology and medicine 127 (1999), S. 123-125 
    ISSN: 1573-8221
    Keywords: myocardial reperfusion ; oxygen radicals ; nitric oxide ; arrhythmias
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract Individual infusion of SOD and NO donor produces an antiarrhythmic effect, although does not completely prevent reperfusion-induced arrhythmias, while the combination of the antiradical agent and NO donor provides the most efficient protection of reperfused myocardium due to summation of their effects.
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