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Psychopharmacology
Article . 1996 . Peer-reviewed
License: Springer TDM
Data sources: Crossref
image/svg+xml Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao Closed Access logo, derived from PLoS Open Access logo. This version with transparent background. http://commons.wikimedia.org/wiki/File:Closed_Access_logo_transparent.svg Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao
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Inhibition of nitric oxide formation reduces voluntary ethanol consumption in the rat

Authors: CALAPAI, Gioacchino; MAZZAGLIA G; SAUTEBIN L; COSTANTINO G; MARCIANO MC; CUZZOCREA, Salvatore; DIROSA M; +1 Authors

Inhibition of nitric oxide formation reduces voluntary ethanol consumption in the rat

Abstract

Brain nitric oxide is involved in the mechanisms that regulate ingestive behavior. To test whether this compound plays a role in alcohol preference, we studied the effects of different doses of NG-nitro-L-arginine (L-NO arg), an inhibitor of nitric oxide synthase (NOS), on voluntary consumption of ethanol and on blood alcohol levels produced by a single intraperitoneal dose of alcohol in the rat. L-NO arg produced a significant and dose-dependent reduction of ethanol intake (P < 0.001) without influencing total fluid consumption or feeding behavior. L-NO arg did not influence the kinetics of alcohol. Our data show that inhibition of nitric oxide formation accompanies reduction of ethanol intake and suggest a possible role for nitric oxide in ethanol self-administration.

Country
Italy
Keywords

Male, Alcohol Drinking, Dose-Response Relationship, Drug, Ethanol, Self Administration, Alcohol; Alcohol intake; Alcohol self-administration; Brain; Ethanol intake; Ethanol self-administration; Nitric oxide;, Nitroarginine, Rats, Rats, Sprague-Dawley, Alcohol; Alcohol self-administration; Alcohol intake; Ntric oxide; Brain, Animals, Alcohol, Alcohol intake, Alcohol self-administration, Brain, Ethanol intake, Ethanol self-administration, Nitric oxide, Enzyme Inhibitors, Nitric Oxide Synthase

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