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  • 标题:Influences of b-endorphins in Ethanol Consumption Patterns and Acquisition of a Conditioned Taste Aversion Mediated by the Drug
  • 本地全文:下载
  • 作者:Paula Abate ; Ximena Caeiro ; Laura Marta Vivas
  • 期刊名称:Revista Argentina de Ciencias del Comportamiento
  • 电子版ISSN:1852-4206
  • 出版年度:2009
  • 卷号:1
  • 期号:1
  • 页码:25-35
  • 语种:Spanish
  • 出版社:National University of Cordoba
  • 摘要:Rewarding effects of ethanol may be mediated in part by endogenous opioids. Ethanol alters b-endorphin synthesis and release. b-endorphin heterozygous (HT) and knockout (KO) mice consume higher levels of a low-concentrated alcohol solution and show heightened predisposition to self-administer ethanol in comparison with wild-type (WT) mice (Grisel et al., 1999). This study was conducted in order to: i) re-analyze and extend previous results in terms of ethanol consumption profiles of b-endorphin deficient mice; and ii) analyze conditioned aversive learning mediated by ethanol postabsorptive effects as a function of genetic capabilities to synthesize b-endorphin. In Experiment 1, mice were evaluated in terms of consumption of a low (7%) ethanol solution in a two-bottle free choice paradigm. Ethanol concentration was then increased to 10 % and voluntary intake consumption was tested. WT mice displayed significantly higher consumption levels and ethanol-preference scores than did KO mice, independently from ethanol concentration. HT mice drank more ethanol than did KO mice. In Experiment 2, mice (KO, HT and WT) were tested in a conditioned taste aversion paradigm in which a sodium chloride (NaCl) solution was paired with a 2-g/kg ethanol dose. Only HT and KO displayed a conditioned aversion when using 2-g/kg ethanol as unconditioned stimulus. The present results indicate that total or partial deficiency of b-endorphin synthesis reduces ethanol preference and consumption, contrary to previous evidences. Furthermore, this study indicates that the lack of b-endorphin synthesis exacerbates ethanol’s aversive postabsorptive effects which can in turn modulate self-administration patterns of the drug.
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