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Moclobemide: evolution, pharmacodynamic, and pharmacokinetic properties.

Abstract
The benzamide moclobemide is a reversible inhibitor of monoamine-oxidase-A (RIMA). It has been extensively evaluated in the treatment of a wide spectrum of depressive disorders and less extensively in anxiety disorders. While clinical aspects will be presented in a subsequent review, this article focuses primarily on moclobemide's evolution, pharmacodynamic and pharmacokinetic properties. In particular, the effects on neurotransmission and intracellular signal transduction, the neuroendocrine system, the tyramine pressure response and animal models of depression are surveyed. In addition, other CNS effects are reviewed with special respect to experimental serotonergic syndrome, anxiolytic and antinociceptive activity, sleep, cognition and driving performance, neuroprotection and seizures.
AuthorsUdo Bonnet
JournalCNS drug reviews (CNS Drug Rev) Vol. 8 Issue 3 Pg. 283-308 ( 2002) ISSN: 1080-563X [Print] United States
PMID12353059 (Publication Type: Journal Article, Review)
Chemical References
  • Antidepressive Agents
  • Monoamine Oxidase Inhibitors
  • Moclobemide
Topics
  • Animals
  • Antidepressive Agents (chemistry, pharmacokinetics, therapeutic use)
  • Anxiety (drug therapy)
  • Cognition Disorders (drug therapy)
  • Depression (drug therapy)
  • Disease Models, Animal
  • Drug Evaluation
  • Humans
  • Moclobemide (chemistry, pharmacokinetics, therapeutic use)
  • Monoamine Oxidase Inhibitors (pharmacokinetics, therapeutic use)
  • Neurosecretory Systems (drug effects, metabolism)
  • Pain (drug therapy)
  • Psychomotor Disorders (drug therapy)
  • Seizures (drug therapy)
  • Signal Transduction (drug effects)
  • Synaptic Transmission (drug effects)
  • Time Factors

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