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痕量胺相关受体1激动剂RO5263397对大鼠可卡因成瘾相关效应的影响。

Effects of the trace amine-associated receptor 1 agonist RO5263397 on abuse-related effects of cocaine in rats.

作者信息

Thorn David A, Jing Li, Qiu Yanyan, Gancarz-Kausch Amy M, Galuska Chad M, Dietz David M, Zhang Yanan, Li Jun-Xu

机构信息

Department of Pharmacology and Toxicology, University at Buffalo, The State University of New York, Buffalo, NY, USA.

1] Department of Pharmacology and Toxicology, University at Buffalo, The State University of New York, Buffalo, NY, USA [2] Department of Physiology and Pathophysiology, Tianjin Medical University, Tianjin, China.

出版信息

Neuropsychopharmacology. 2014 Sep;39(10):2309-16. doi: 10.1038/npp.2014.91. Epub 2014 Apr 18.

Abstract

Animal knockout studies suggest that trace amine-associated receptor (TAAR) 1 is involved in behavioral effects of psychostimulants such as cocaine. Recently, several highly selective TAAR 1 agonists have been discovered. However, little is known of the impact of TAAR 1 agonists on abuse-related effects of cocaine. Here, we report the effects of a TAAR 1 agonist RO5263397 on several abuse-related behavioral effects of cocaine in rats. RO5263397 was evaluated for its effects on cocaine-induced behavioral sensitization, conditioned place preference (CPP), cue- and cocaine prime-induced reinstatement of cocaine-seeking behavior, and cocaine self-administration using behavioral economic analysis. RO5263397 reduced the expression of cocaine behavioral sensitization, cue- and cocaine prime-induced reinstatement of cocaine seeking, and expression but not development of cocaine CPP. Behavioral economic analysis showed that RO5263397 increased the elasticity of the cocaine demand curve, but did not change cocaine consumption at minimal prices. Taken together, this is the first systematic assessment of a TAAR 1 agonist on a range of behavioral effects of cocaine, showing that RO5263397 was efficacious in reducing cocaine-mediated behaviors. Collectively, these data uncover essential neuromodulatory roles of TAAR 1 on cocaine abuse, and suggest that TAAR 1 may represent a novel drug target for the treatment of cocaine addiction.

摘要

动物基因敲除研究表明,痕量胺相关受体(TAAR)1与可卡因等精神兴奋剂的行为效应有关。最近,已发现几种高选择性TAAR 1激动剂。然而,关于TAAR 1激动剂对可卡因滥用相关效应的影响却知之甚少。在此,我们报告了TAAR 1激动剂RO5263397对大鼠可卡因几种滥用相关行为效应的影响。使用行为经济学分析评估了RO5263397对可卡因诱导的行为敏化、条件性位置偏爱(CPP)、线索和可卡因激发诱导的可卡因觅求行为恢复以及可卡因自我给药的影响。RO5263397降低了可卡因行为敏化的表达、线索和可卡因激发诱导的可卡因觅求行为恢复以及可卡因CPP的表达,但不影响其形成。行为经济学分析表明,RO5263397增加了可卡因需求曲线的弹性,但在最低价格时不改变可卡因的消耗量。综上所述,这是对TAAR 1激动剂对可卡因一系列行为效应的首次系统评估,表明RO5263397在减少可卡因介导的行为方面是有效的。总体而言,这些数据揭示了TAAR 1在可卡因滥用中的重要神经调节作用,并表明TAAR 1可能代表治疗可卡因成瘾的一个新的药物靶点。

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