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| Research article summary (published 22 Oct 2006): |
The CB1 cannabinoid receptor antagonist rimonabant chronically prevents the nicotine-induced relapse to alcohol.
Full Abstract
Preclinical and clinical research shows that the cannabinoid brain receptor type 1 (CB(1)) modulates alcohol- and nicotine-related behaviors. Throughout the nicotine-induced relapse to alcohol, the rats were pre-treated for 10 days with the CB(1) cannabinoid receptor antagonist rimonabant (0, 0.03, 0.3 and 3.0 mg/kg i.p.). In this condition, a long-lasting nicotine-induced relapse to alcohol was observed, and this effect was reversed in a dose-dependent manner with rimonabant. Surprisingly, rats that were not exposed to nicotine developed tolerance to the effects of rimonabant from the sixth day. Also, 3.0 mg/kg of rimonabant reduced the responses for sucrose. Evaluation in the Elevated Plus-Maze after nicotine treatment did not reveal anxiogenic effects. Finally, at the conclusion of rimonabant treatment, a rapid reinstatement of alcohol consumption was detected. These results suggest that rimonabant can prevent the relapse to alcohol, even when an interaction with nicotine exists-the most frequent situation in human alcohol abuse.
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Author information
Author/s: López-Moreno, José Antonio (JA); González-Cuevas, Gustavo (G); Navarro, Miguel (M);
Affiliation: Department of Psychobiology, Faculty of Psychology, Campus de Somosaguas, Complutense University of Madrid, 28223 Madrid, Spain. jalopezm(-atsign-)psi.ucm.es
Journal and publication information
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
Journal: Neurobiology of disease (Neurobiol Dis), published in United States. (Language: eng)
Reference: 2007-Feb; vol 25 (issue 2) : pp 274-83
Dates: Created 2007/01/26; Completed 2007/04/11; Revised 2007/10/17;
PMID: 17067804, status: MEDLINE (last retrieval date: 12/26/2008)
Sourced from the National Library of Medicine. Abstract text and other information may be subject to copyright.
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