Ethanol-induced sensitization depends preferentially on D(1) rather than D(2) dopamine receptors


Autoria(s): CAMARINI, Rosana; MARCOURAKIS, Tania; TEODOROV, Elizabeth; YONAMINE, Mauricio; CALIL, Helena Maria
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

20/10/2012

20/10/2012

2011

Resumo

Behavioral sensitization, defined as a progressive increase in the locomotor stimulant effects elicited by repeated exposure to drugs of abuse, has been used as an animal model for drug craving in humans. The mesoaccumbens dopaminergic system has been proposed to be critically involved in this phenomenon; however, few studies have been designed to systematically investigate the effects of dopaminergic antagonists on development and expression of behavioral sensitization to ethanol in Swiss mice. We first tested the effects of D(1) antagonist SCH-23390 (0-0.03 mg/kg) or D(2) antagonist Sulpiride (0-30 mg/kg) on the locomotor responses to an acute injection of ethanol (2.0 g/kg). Results showed that all tested doses of the antagonists were effective in blocking ethanol`s stimulant effects. In another set of experiments, mice were pretreated intraperitoneally with SCH-23390 (0.01 mg/kg) or Sulpiride (10 mg/kg) 30 min before saline or ethanol injection, for 21 days. Locomotor activity was measured weekly for 20 min. Four days following this pretreatment, all mice were challenged with ethanol. Both antagonists attenuated the development of ethanol sensitization, but only SCH-23390 blocked the expression of ethanol sensitization according to this protocol. When we tested a single dose (30 min before tests) of either antagonist in mice treated chronically with ethanol, both antagonists attenuated ethanol-induced effects. The present findings demonstrate that the concomitant administration of ethanol with D(1) but not D(2) antagonist prevented the expression of ethanol sensitization, suggesting that the neuroadaptations underlying ethanol behavioral sensitization depend preferentially on D(1) receptor actions. (C) 2010 Elsevier Inc. All rights reserved.

Fundacao de Amparo a Pesquisa do Estado de Sao Paulo (FAPESP)

Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)

Conselho Nacional de Desenvolvimento Cientifico e Tecnologico (CNPq)

Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)

Identificador

PHARMACOLOGY, BIOCHEMISTRY AND BEHAVIOR, v.98, n.2, p.173-180, 2011

0091-3057

http://producao.usp.br/handle/BDPI/28142

10.1016/j.pbb.2010.12.017

http://dx.doi.org/10.1016/j.pbb.2010.12.017

Idioma(s)

eng

Publicador

PERGAMON-ELSEVIER SCIENCE LTD

Relação

Pharmacology, Biochemistry and Behavior

Direitos

restrictedAccess

Copyright PERGAMON-ELSEVIER SCIENCE LTD

Palavras-Chave #Ethanol #Behavioral sensitization #SCH-23390 #Sulpiride #Dopamine receptor antagonist #Mice #CONDITIONED PLACE PREFERENCE #VENTRAL TEGMENTAL AREA #INDUCED LOCOMOTOR STIMULATION #FREELY MOVING RATS #BEHAVIORAL SENSITIZATION #NUCLEUS-ACCUMBENS #SELECTIVE D1 #COCAINE SENSITIZATION #DBA/2J MICE #OPEN-FIELD #Behavioral Sciences #Neurosciences #Pharmacology & Pharmacy
Tipo

article

original article

publishedVersion