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  • Chemistry  (5)
  • Cobalt staining  (1)
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  • 1
    ISSN: 1432-1351
    Keywords: Cobalt staining ; Gas chromatography-mass spectrometry ; Immunohistochemistry ; Insect ; Neuromodulation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract The two Protocerebral-Medulla 4 neurons (PM4a and b) in the locust brain have adjacent cell bodies in the medial deutocerebrum. They project through the posterior protocerebrum, forming limited arborisations en route, and enter the lobula and medulla of the ipsilateral optic lobe, where they form extensive, overlapping arborisations. The PM4a and b neurons are octopamine immunoreactive. Their octopamine content (approximately 25 pg per cell) is confirmed by gas chromatography-mass spectrometry; each cell contains approximately 25 pg p-octopamine. Simultaneous intracellular recording from exposed PM4a and b cell bodies reveals that the two cells are physiologically indistinguishable. They receive multimodal sensory inputs. Tactile/mechanosensory stimuli to much of the animal's body and head, acoustic stimuli, and simple visual stimuli all give rise to e.p.s.p.s and action potentials in the PM4 cell body. Simultaneous recording from the cell body in the deutocerebrum and the axon in the lobula demonstrates that action potentials are predominantly initiated in the deutocerebrum and propagate centrifugally, towards the optic lobe. Occasionally, bright light flashes will initiate an action potential in the axon in the optic stalk, which probably propagates bidirectionally: centripetally to the cell body, and centrifugally into the optic lobe. The extensive arborisations in the lobula and medulla are therefore likely to be sites of octopamine release. Because PM4 neurons are octopaminergic, project to the optic lobe, and receive modalities of sensory input known to dishabituate the Descending Contralateral Movement Detector (DCMD) visual interneuron, it is proposed that PM4 neurons are neuromodulatory — mediating dishabituation or arousal of the visual system.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Rapid Communications in Mass Spectrometry 3 (1989), S. 8-10 
    ISSN: 0951-4198
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Physics
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Rapid Communications in Mass Spectrometry 4 (1990), S. 34-36 
    ISSN: 0951-4198
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Physics
    Notes: Oxazolidinone derivatives of glycine, phenylalanine and tyrosine were prepared by their reaction with dichlorotetrafluoroacetone. The derivatives were analyzed by gas chromatography/negative-ion chemicalionization mass spectrometry with methane as the reagent gas. The mass spectra under these conditions were composed of a few ions resulting largely from the addition of a chlorine radical to the molecular ion and successive losses of up to two HCl moieties from the molecular ion; loss of CO2 was also observed. Comparison of the mass spectrum of glycine and [2H2]glycine indicated that the protons involved in the loss of HCl from the molecular ion were derived in the first instance from the CH2 group in the derivative and secondly from the NH group. The derivatives were applied to the analysis of the amino acid precursors of biogenic amines in nervous tissue from the locust.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 0887-6134
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Prednisolone, dexamethasone and betamethasone were labelled with deuterium via a simple synthetic procedure and used as internal standards in the gas chromatographic/mass spectrometric analysis of the corresponding undeuterated compounds. The mass spectrometer was used in the negative chemical ionization mode, which gave fragmentation of the methoxime trimethylsilyl ether derivatives favourable for their quantification. The method was applicable to the quantification of synthetic corticosteroids contained in human aqueous humour in the 0.1-10-ng range.
    Additional Material: 7 Ill.
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  • 5
    ISSN: 0887-6134
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Pentafluorobenzyl hydroxylamine has been used as a derivatization reagent in the analysis of corticosteroids by gas chromatography/negative ion chemical ionization (GC/NICI) mass spectrometry. The resulting pentafluorobenzyloxime-trimethylsilyl (PFBO/TMS) derivatives were generally formed in moderate yield but, despite this, the use of these derivatives resulted in a ∼ 10-fold improvement in the capability of identification of corticosteroids by GC/NICI mass spectrometry in comparison with the methoxime/TMS derivatives previously employed. The NICI mass spectra of PFBO/TMS derivatives were simple, with most of the ion current being carried by the [M - C6F6CH2]-. or [M - PFB]-. ion and by a reagent-specific peak at m/z 196. The derivatives have been employed in the quantification of ∼400 pg amounts of endogenous hydrocortisone present in samples of human aqueous humour and are readily applicable to the determination of low-picogram amounts of these compounds in biological media.
    Additional Material: 5 Ill.
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  • 6
    ISSN: 0887-6134
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: An extraction-derivatization method suitable for the analysis of subnanogram amounts of biogenic amines in aqueous solution has been developed. The most satisfactory procedure for the analysis of these compounds was reaction with 3,5-ditrifluorobenzoylchloride (DTFMBCl) in phosphate buffer at pH 7.2 followed by extraction of the resultant amide esters into ethyl acetate. This was followed by hydrolysis of the phenolic ester functionalities by shaking the organic layer with 10 M ammonium hydroxide. The phenolic and alcoholic hydroxyl groups were then reacted with bistrimethylsilylacetamide and the trimethylsilyl-DTFMB amides were then analysed by gas chromatography/mass spectrometry in the negative ion chemical ionization mode with methane as reagent gas. The limits of detection for these derivatives was 〈1 pg and the method was readily applicable to the extraction and analysis of 0.5 ng of a given biogenic amine.
    Additional Material: 7 Ill.
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