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  • 1
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature 249 (1974), S. 476-478 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] Male albino rats of Wistar origin (Fullinsdorf), 180-200 g, were injected with an aqueous solution of BH4 into one lateral brain ventricle (30-1,000 Mg in 10 /4 through a chronically implanted cannula10) or intravenously (125 mg kg-1)- The solutions contained 1 % ascorbic acid. o At various time ...
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  • 2
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature 278 (1979), S. 563-565 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] From acetone or HC1O4 extracts of bovine or rat brain, three compounds were isolated by conventional column chromato-graphy and identified by mass spectrometry, which showed some, although rather low, potency in inhibiting specific binding of 3H-diazepam to the benzodiazepine high-affinity binding ...
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Cellular and molecular life sciences 40 (1984), S. 1165-1172 
    ISSN: 1420-9071
    Keywords: Pharmacology of Parkinson's disease ; antiparkinson drugs ; benserazide ; carbidopa ; L-DOPA ; dopamine receptor agonists ; (−)deprenyl ; MAO-B inhibitors
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary Basic aspects and recent advances in the understanding of the pharmacological mechanism of action of the clinically most used antiparkinson drugs are reviewed. Recent human and animal biochemical investigations clearly confirm and extend previous findings indicating that benserazide is much more potent than carbidopa as peripheral decarboxylase inhibitor. L-DOPA in combination with benserazide or carbidopa constitutes the best available therapy for Parkinson's disease (PD). To reduce peaks and rapid fluctuations of L-DOPA plasma levels (possibly responsible for peak-dose dyskinesias and end-of-dose deterioration) a slow-release formulation of L-DOPA in combination with benserazide or with benserazide plus catechol-O-methyltransferase inhibitors should be developed. In parkinsonian patients under long-term L-DOPA therapy monoamine oxidase inhibitors type B (MAO-B) e.g. (−)-deprenyl and firect dopamine receptor agonists (bromocriptine, lisuride, pergolide etc.), due to their L-DOPA-sparing effects, alleviate in some cases L-DOPA-induced side-effects e.g. dyskinesias and on-off phenomena. However, since (−)-deprenylm, due to its metabolism to (−)methamphetamine and (−)amphetamine, seem to have indirect sympathomimetic activity, new selective MAO-B inhibitors devoid of indirect sympathomimetic effects should be tested clinically to assess the functional role of pure MAO-B inhibition in the therapy of PD. The auxiliary therapy with direct dopmaine receptor agonists of the D-2 subtype represents another valid approach which should be further investigated in order to find novel dopamine agonists, less expensive than bromocriptine and strictly selective for D-2 receptor sites.
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Insectes sociaux 42 (1995), S. 145-156 
    ISSN: 1420-9098
    Keywords: Macrotermes ; alarm response ; recruitment
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary In laboratory studies we analysed the reaction of aMacrotermes subhyalinus (Rambur) colony in contact with a small group of test termites placed at the head of a gallery system. As test termites we usedMacrotermes subhyalinus of the same nest,Macrotermes subhyalinus of a foreign nest and the related sympatric speciesMacrotermes bellicosus (Smeathman). Contact with an introduced group of foragers evokes a significant recruitment of workers and minor soldiers. The intensity of the response depends on the test groups we introduced. The highest recruitment results withM. bellicosus andM. subhyalinus from a foreign nest. During the recruitment the increase in the number of minor soldiers is greater than the increase in the number of workers, and as a result, the relative proportion of the soldiers in the population leaving the nest is significantly higher than before. Direct observations at the place of contact show thatM. bellicosus individuals are immediately attacked and killed. In the case ofM. subhyalinus from a foreign nest, not all individuals are killed; some are only intensively examined with the antennae or seized with the mandibles.M. subhyalinus from the same nest are rarely attacked. Mostly they are antennally inspected or enter the gallery system unhindered. The recruitment of termites from the nest is released by major workers which, after contact with the test termites, run back into the nest and provoke an alarm by tactile stimuli. On their way back into the nest the major workers, in all probability, lay a pheromone trail which leads the outgoing alarmed termites towards the place of contact.
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  • 5
    ISSN: 1432-1041
    Keywords: moclobemide ; Ro 11-1163 ; pharmacokinetics ; bioavailability ; MAO activity in platelets ; monoamine metabolites in urine ; healthy volunteers
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Medicine
    Notes: Summary The plasma concentrations of the MAO-inhibitor moclobemide (Ro 11-1163) were determined in six healthy male subjects after oral (tablets) administration. Effects on MAO activity in platelets and excretion of monoamine metabolites in urine were investigated. The design of the study was a double-blind cross-over study with single oral doses of placebo, 50, 100 and 200 mg of moclobemide. The elimination profile of the drug showed that the half life of the unchanged drug ranged between 1 and 2 h except in one subject with a half-life of about 4 h. The mean bioavailability calculated using flow model concepts was F=0.43 after 50 mg, F=0.47 after 100 mg and F=0.59 after 200 mg. The outlier with a t1/2 of 4 h was found to have a bioavailability of more than 0.80 after all 3 doses. The slightly increasing bioavailability with higher doses was interpreted as evidence of saturable hepatic first-pass elimination of the drug. MAO activity in platelets was measured before and 2, 6 and 24 h after drug administration. No inhibition of platelet MAO was obtained at any point in time or dose level, as to be expected since moclobemide preferentially inhibits MAO A. Urine excretion of the monoamine metabolites homovanillic acid (HVA), dihydroxyphenylacetic acid (DOPAC), 3-methoxy-4-hydroxy-phenylglycol (MOPEG) and 5-hydroxyindoleacetic acid (5-HIAA) was followed during 48 h after placebo, 50 and 200 mg of moclobemide. Time but not dose contributed significantly to the variability in excretion of the monoamine metabolites. An apparent reduction of HVA and DOPAC levels was obtained in the early phase after the administration of 200 mg of moclobemide. In 1 subject with a mild drug reaction a pronounced decrease in the levels of all the metabolites was obtained. In the other 5 subjects, the compound was very well tolerated with a few reported side-effects like increased activity, somnolence or sweatings. There was a slight but significant increase in blood pressure following 50 and 100 mg but not 200 mg of moclobemide.
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  • 6
    ISSN: 1432-1041
    Keywords: Monoamine oxidase type B ; Positron emission tomography ; Ro 19-6327 ; Pharmacodynamics
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Medicine
    Notes: Summary Eight normal subjects (3 females and 5 males) were studied using intravenous L-11C] deprenyl and positron emission tomography. In a single blind study one subject received tracer alone, one subject received an oral pre-dose of 20 mg of L-deprenyl and 6 subjects received oral pre-doses of 10 to 50 mg of a novel reversible MAO-B inhibitor (Ro 19-6327). Dynamic PET scans beginning 12 h after the oral dose were collected over 90 min and arterial blood was continuously sampled. Data analysis was modelled for two tissue compartments and using an iterative curve fitting technique the value of the rate constant for irreversible binding of L-[11C] deprenyl to MAO-B (k3) in whole brain was obtained for each subject. The dose response curves obtained indicated that a dose of at least 0.48 mg·kg−1 of Ro 19-6327 was necessary for 〉90% decrease in whole brain k3. Inhibition of MAO-B in platelets isolated from blood samples taken at the time of scanning correlated strongly with decrease in whole brain k3 (r=0.949). The results indicate that PET can be used to determine the dose of Ro 19-6327 necessary to inhibit 〉90% of brain MAO-B. This technique is an attractive alternative to traditional large scale patient-based dose-finding studies. Moreover it is shown that inhibition of platelet MAO-B can be used as a marker for central MAO-B inhibition with Ro 19-6327.
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    Behavioral ecology and sociobiology 27 (1990), S. 17-21 
    ISSN: 1432-0762
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary In a shoal of four sticklebacks (Gasterosteus aculeatus) individual fish had partners with whom they repeatedly performed pairwise predator inspection visits. In six different trials, we found two reciprocal pairs per trial significantly more often than would be expected by chance. These results provide further evidence for a TIT FOR TAT like cooperation strategy in sticklebacks.
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  • 8
    Publication Date: 2001-07-31
    Print ISSN: 0027-8424
    Electronic ISSN: 1091-6490
    Topics: Biology , Medicine , Natural Sciences in General
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  • 9
    Publication Date: 2013-09-24
    Description: Earthquakes along convergent plate boundaries commonly occur in sequences that are complete within 1 yr, and may include 8–10 events strong enough to generate sand blows. Dune crossbeds within the Jurassic Navajo Sandstone of Utah (western United States) enclose intact and truncated sand blows, and the intrusive structures that fed them. We mapped the distribution of more than 800 soft-sediment dikes and pipes at two small sites. All water-escape structures intersect a single paleo-surface, and are limited to the upper portion of the underlying set of cross-strata and the lower portion of the overlying set. A small portion of one set of crossbeds that represents ~1 yr of dune migration encloses eight generations of eruptive events. We interpret these superimposed depositional and deformational structures as the record of a single shock-aftershock earthquake sequence. The completeness and temporal detail of this paleoseismic record are unique, and were made possible when sand blows repeatedly erupted onto lee slopes of migrating dunes. Similar records should be sought in modern dunefields with shallow water tables.
    Print ISSN: 0091-7613
    Electronic ISSN: 1943-2682
    Topics: Geosciences
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  • 10
    Publication Date: 1971-07-01
    Print ISSN: 0027-8424
    Electronic ISSN: 1091-6490
    Topics: Biology , Medicine , Natural Sciences in General
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