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HERO ID
502817
Reference Type
Journal Article
Title
Central side-effects of therapies based on CB1 cannabinoid receptor agonists and antagonists: focus on anxiety and depression
Author(s)
Moreira, FA; Grieb, M; Lutz, B
Year
2009
Is Peer Reviewed?
Yes
Journal
Best Practice and Research: Clinical Endocrinology and Metabolism
ISSN:
1521-690X
EISSN:
1532-1908
Volume
23
Issue
1
Page Numbers
133-144
Language
English
DOI
10.1016/j.beem.2008.09.003
Abstract
Both agonists (e.g. Delta(9)-tetrahydrocannabinol, nabilone) and antagonists (e.g. rimonabant, taranabant) of the cannabinoid type-1 (CB1) receptor have been explored as therapeutic agents in diverse fields of medicine Such as pain management and obesity with associated metabolic dysregulation, respectively. CB, receptors are widely distributed in the central nervous system and are involved in the modulation of emotion, stress and habituation responses, behaviours that are thought to be dysregulated in human psychiatric disorders. Accordingly, CB1 receptor activation may, in some cases, precipitate episodes of psychosis and panic, while its inhibition may lead to behaviours reminiscent of depression and anxiety-related disorders. The present review discusses these side-effects, which have to be taken into account in the therapeutic exploitation of the endocannabinoid system. (C) 2008 Elsevier Ltd. All rights reserved.
Keywords
cannabinoids; anxiety; depression; Sativex; dronabinol; nabilone; rimonabant; taranabant; randomized controlled-trial; antidepressant-like activity; medial; prefrontal cortex; lithium-paired context; pituitary-adrenal axis; endocannabinoid system; multiple-sclerosis; inverse agonist; anxiolytic-like; risk-factors
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