Please use this identifier to cite or link to this item: https://repositorio.unifesp.br/handle/11600/33568
Title: Ethanol-induced sensitization depends preferentially on D-1 rather than D-2 dopamine receptors
Authors: Camarini, Rosana [UNIFESP]
Marcourakis, Tania
Teodorov, Elizabeth
Yonamine, Mauricio
Calil, Helena Maria [UNIFESP]
Universidade de São Paulo (USP)
Universidade Federal do ABC (UFABC)
Universidade Federal de São Paulo (UNIFESP)
Keywords: Ethanol
Behavioral sensitization
SCH-23390
Sulpiride
Dopamine receptor antagonist
Mice
Issue Date: 1-Apr-2011
Publisher: Elsevier B.V.
Citation: Pharmacology Biochemistry and Behavior. Oxford: Pergamon-Elsevier B.V., v. 98, n. 2, p. 173-180, 2011.
Abstract: 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.
URI: http://repositorio.unifesp.br/handle/11600/33568
ISSN: 0091-3057
Other Identifiers: http://dx.doi.org/10.1016/j.pbb.2010.12.017
Appears in Collections:Em verificação - Geral

Files in This Item:
File Description SizeFormat 
WOS000289396300002.pdf407.86 kBAdobe PDFView/Open


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.