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可卡因位置偏爱可被δ-阿片受体拮抗剂纳曲吲哚阻断。

Cocaine place preference is blocked by the delta-opioid receptor antagonist, naltrindole.

作者信息

Menkens K, Bilsky E J, Wild K D, Portoghese P S, Reid L D, Porreca F

机构信息

Department of Pharmacology, University of Arizona Health Sciences Center, Tucson 85724.

出版信息

Eur J Pharmacol. 1992 Aug 25;219(2):345-6. doi: 10.1016/0014-2999(92)90319-y.

Abstract

Naltrindole, a selective delta-opioid receptor antagonist, was evaluated for its potential to block the reinforcing properties of cocaine using a conditioned place pairing paradigm in Lewis rats. Cocaine HCl (15 mg/kg s.c.) produced a strong place preference which was significantly blocked in animals pretreated with naltrindole (3 mg/kg i.p.); naltrindole alone showed no reinforcing or aversive effects. The results suggest a novel approach for the treatment of cocaine abuse in man.

摘要

纳曲吲哚是一种选择性δ阿片受体拮抗剂,利用条件性位置配对范式在Lewis大鼠中评估了其阻断可卡因强化特性的潜力。盐酸可卡因(15毫克/千克,皮下注射)产生了强烈的位置偏爱,而在用纳曲吲哚(3毫克/千克,腹腔注射)预处理的动物中,这种偏爱被显著阻断;单独使用纳曲吲哚未显示出强化或厌恶作用。这些结果提示了一种治疗人类可卡因成瘾的新方法。

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