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κ-阿片受体激动剂U-69593可减轻可卡因诱导的大鼠行为敏化。

The kappa-opioid receptor agonist U-69593 attenuates cocaine-induced behavioral sensitization in the rat.

作者信息

Heidbreder C A, Goldberg S R, Shippenberg T S

机构信息

Behavioral Pharmacology and Genetics Section, National Institute on Drug Abuse, Baltimore, MD 21224.

出版信息

Brain Res. 1993 Jul 9;616(1-2):335-8. doi: 10.1016/0006-8993(93)90228-f.

Abstract

The effects of treatment with the selective kappa-opioid receptor agonist U-69593 upon cocaine-induced changes in locomotor activity and stereotypy were examined in rats. U-69593 (0.16 mg/kg s.c.) administered either acutely or chronically attenuated both the motor stimulant effect and stereotypy produced by an acute injection of cocaine (20 mg/kg i.p.). Daily cocaine treatment resulted in sensitization to both effects of cocaine. In contrast, no such sensitized responses were seen in animals which had received U-69593 either prior to or in conjunction with daily cocaine treatment. These data demonstrate that activation of kappa-opioid receptors attenuates the acute and chronic effects of cocaine on locomotor activity and stereotypy. Given the inhibitory effects ascribed to both exogenous and endogenous kappa-opioid agonists upon dopamine release in the mesolimbic dopaminergic system, it is suggested that this action may underlie the observed effects of U-69593 on cocaine-induced changes in locomotor activity and stereotypy.

摘要

在大鼠中研究了选择性κ-阿片受体激动剂U-69593对可卡因诱导的运动活性和刻板行为变化的治疗效果。急性或慢性给予U-69593(0.16mg/kg皮下注射)均可减弱急性注射可卡因(20mg/kg腹腔注射)所产生的运动兴奋作用和刻板行为。每日给予可卡因会导致对可卡因两种作用的敏感化。相比之下,在每日给予可卡因之前或同时接受U-69593治疗的动物中未观察到这种敏感化反应。这些数据表明,κ-阿片受体的激活减弱了可卡因对运动活性和刻板行为的急性和慢性作用。鉴于外源性和内源性κ-阿片激动剂对中脑边缘多巴胺能系统中多巴胺释放均有抑制作用,提示该作用可能是U-69593对可卡因诱导的运动活性和刻板行为变化产生观察到的效果的基础。

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