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育亨宾会加剧而可乐定可减轻大鼠的急性吗啡戒断反应。

Yohimbine exacerbates and clonidine attenuates acute morphine withdrawal in rats.

作者信息

Dwoskin L P, Neal B S, Sparber S B

出版信息

Eur J Pharmacol. 1983 Jun 3;90(2-3):269-73. doi: 10.1016/0014-2999(83)90248-0.

Abstract

The involvement of alpha 2-noradrenergic receptors in the expression of opiate withdrawal was studied using an operant behavioral model of acute morphine dependence. Clonidine, an alpha 2-agonist, attenuated and yohimbine, an alpha 2-antagonist, exacerbated the naloxone-induced suppression of fixed ratio 15 responding in rats pretreated several hours earlier with a single, moderate dose of morphine. These data indicate that the alpha 2-agonist action of clonidine is responsible for its amelioration of withdrawal symptoms. It also validates the acute dependence model for studying the pharmacology of opiates and associated adaptive processes.

摘要

使用急性吗啡依赖的操作性行为模型,研究了α2-去甲肾上腺素能受体在阿片类药物戒断表达中的作用。α2激动剂可乐定可减轻戒断反应,而α2拮抗剂育亨宾则会加剧戒断反应。在数小时前接受单次中等剂量吗啡预处理的大鼠中,可乐定减弱了纳洛酮诱导的固定比率15反应抑制,而育亨宾则加剧了这种抑制。这些数据表明,可乐定的α2激动剂作用是其改善戒断症状的原因。这也验证了用于研究阿片类药物药理学及相关适应性过程的急性依赖模型。

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