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D1类和D2类多巴胺受体激动剂对觅可卡因行为的相反调节作用。

Opposite modulation of cocaine-seeking behavior by D1- and D2-like dopamine receptor agonists.

作者信息

Self D W, Barnhart W J, Lehman D A, Nestler E J

机构信息

Laboratory of Molecular Psychiatry, Department of Psychiatry, Yale University School of Medicine, Connecticut Mental Health Center, New Haven, 06508, USA.

出版信息

Science. 1996 Mar 15;271(5255):1586-9. doi: 10.1126/science.271.5255.1586.

Abstract

Activation of the mesolimbic dopamine system is known to trigger relapse in animal models of cocaine-seeking behavior. We found that this "priming" effect was selectively induced by D2-like, and not by D1-like, dopamine receptor agonists in rats. Moreover, D1-like receptor agonists prevented cocaine-seeking behavior induced by cocaine itself, whereas D2-like receptor agonists enhanced this behavior. These results demonstrate an important dissociation between D1- and D2-like receptor processes in cocaine-seeking behavior and support further evaluation of D1-like receptor agonists as a possible pharmacotherapy for cocaine addiction.

摘要

已知中脑边缘多巴胺系统的激活会在可卡因寻求行为的动物模型中引发复吸。我们发现,这种“启动”效应在大鼠中是由D2样而非D1样多巴胺受体激动剂选择性诱导的。此外,D1样受体激动剂可预防可卡因自身诱导的可卡因寻求行为,而D2样受体激动剂则增强这种行为。这些结果表明,在可卡因寻求行为中,D1样和D2样受体过程存在重要的分离,并支持进一步评估D1样受体激动剂作为可卡因成瘾可能的药物治疗方法。

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