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海洛因在μ-阿片受体缺陷小鼠中诱导的奖赏缺失和运动刺激缺乏。

Lack of reward and locomotor stimulation induced by heroin in mu-opioid receptor-deficient mice.

作者信息

Contarino Angelo, Picetti Roberto, Matthes Hans W, Koob George F, Kieffer Brigitte L, Gold Lisa H

机构信息

Department of Neuropharmacology, The Scripps Research Institute, 10550 North Torrey Pines Rd, La Jolla, CA 92037, USA.

出版信息

Eur J Pharmacol. 2002 Jun 20;446(1-3):103-9. doi: 10.1016/s0014-2999(02)01812-5.

Abstract

The micro-opioid receptor is the main substrate mediating opiate reward. Multiple micro-opioid receptor subtypes have been postulated to underlie opiate actions. Animals treated with antisense oligonucleotides targeting specific micro-opioid receptor exons show differential sensitivity to morphine versus heroin. The present work examined the rewarding and locomotor activating effects of heroin in mutant mice with a disrupted exon 2 of the micro-opioid receptor. Heroin (1-3 mg/kg) produced significant place preferences and stimulated locomotor activity in wild-type mice, whereas it had no effect in micro-opioid receptor-deficient mice. In contrast, treatment with cocaine (10-30 mg/kg) produced comparable place preferences and locomotor activation in both wild-type and micro-opioid receptor-deficient mice, thus providing evidence that the mutant mice are able to show drug-induced effects in the two behavioral paradigms used here. These results support an essential role for the micro-opioid receptor in the rewarding and locomotor activating effects of heroin.

摘要

微阿片受体是介导阿片奖赏作用的主要底物。已推测多种微阿片受体亚型是阿片作用的基础。用针对特定微阿片受体外显子的反义寡核苷酸处理的动物对吗啡和海洛因表现出不同的敏感性。本研究检测了海洛因对微阿片受体外显子2缺失的突变小鼠的奖赏和运动激活作用。海洛因(1 - 3毫克/千克)在野生型小鼠中产生显著的位置偏爱并刺激运动活性,而在微阿片受体缺陷小鼠中则无此作用。相比之下,可卡因(10 - 30毫克/千克)处理在野生型和微阿片受体缺陷小鼠中均产生了相当的位置偏爱和运动激活,从而证明突变小鼠在此处使用的两种行为范式中能够表现出药物诱导的效应。这些结果支持微阿片受体在海洛因的奖赏和运动激活作用中起关键作用。

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