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Titlebook: Amine Oxidases and Their Impact on Neurobiology; Proceedings of the 4 Peter Riederer,Moussa B. H. Youdim Conference proceedings 1990 Spring

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In vivo studies on the effect of monoamine oxidase inhibitors on dopamine and serotonin metabolism iIn vivo voltammetric analyses on the action of the monoamine oxidase inhibitors pargyline, deprenyl, and clorgyline on dopamine and serotonin metabolism in rat brain showed strain and regional differences depending on the compound under study.
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,Die Identität Tirols in der EU,nimals and in humans. Lack of absolute specificity of enzymes, storage mechanisms and transporters allows .C-or .F-labelled “false transmitters” to be formed, stored and released from nerve terminals. Discussed are the assumptions, limitations, and advantages of .F-6-fluoroDOPA, .F-6-fluorodopamine,
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https://doi.org/10.1007/978-3-211-73754-5n the mechanism of action of antidepressants. Due to these investigations, until recently an enhanced activity of the central noradrenergic and/or serotonergic transmitter system was considered essential for the clinical antidepressive action. Such enhancement could be achieved either presynapticall
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Problemstellung und Zielsetzungirreversible ligand, which bind stoichiometrically to the enzyme. A tracer dose of. C-L-deprenyl was injected and PET scans performed to obtain baseline deprenyl binding. A high dose of unlabelled deprenyl was then administered to inhibit the enzyme and tracer doses of . C-L-deprenyl, with subsequen
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https://doi.org/10.1007/978-3-662-67441-3nd 3 brains from patients with Alzheimer’s disease (AD). High .H-L-deprenyl binding was found in e.g. basal ganglia, cingulate gyrus, and insula cortex. Temporal cortex, parietal cortex, occipital cortex and various nuclei of the thalamus, showed moderate density, while low binding was observed in e
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