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美沙酮(μ型)耐受大鼠与乙基酮环唑辛(κ型)耐受大鼠之间的双向交叉耐受性。

Bidirectional cross-tolerance between methadone (mu)- and ethylketocyclazocine (kappa)-tolerant rats.

作者信息

Hong O, Young G A, Khazan N

出版信息

Drug Alcohol Depend. 1986 Sep;18(1):87-96. doi: 10.1016/0376-8716(86)90117-1.

Abstract

Our laboratory previously reported on unidirectional cross-tolerance between morphine and methadone, both mu opioid agonists, and between morphine and ethylketocyclazocine (EKC), the latter being a relatively selective kappa opioid agonist. Morphine-tolerant rats were found to be non-cross-tolerant to methadone and EKC, but methadone- and EKC-tolerant rats were cross tolerant to morphine. In the present study, we characterized the cross-tolerance between methadone and EKC. A group of female adult Sprague-Dawley rats was made tolerant to methadone by a series of automatic i.v. injections ranging from 0.25 mg/kg per 2 h on the first day to 2.0 mg/kg per 1.5 h on the ninth day. Another group of rats was similarly made tolerant to EKC with doses ranging from 0.5 mg/kg per 2 h on the first day to 4 mg/kg per h on the ninth day. Relatively similar degrees of tolerance development to the EEG and behavioral effects of methadone and EKC were reflected by decreases in durations of action and decreases in opioid-induced EEG power spectral changes. Methadone-tolerant rats were found to be cross-tolerant to the EEG and behavioral effects of EKC, and, similarly, EKC-tolerant rats were found to be cross-tolerant to those of methadone. Thus, a bidirectional cross-tolerance between a mu and a kappa agonist was demonstrated. The present results together with those reported earlier indicate that cross-tolerance may not be directly related to the receptor selectivity of the opioids. It is possible that differential physicochemical properties of these opioids may play a more decisive role in the phenomenon of cross-tolerance.

摘要

我们实验室之前报道过,吗啡和美沙酮(二者均为μ阿片受体激动剂)之间以及吗啡和乙基酮环唑辛(EKC,后者是一种相对选择性的κ阿片受体激动剂)之间存在单向交叉耐受性。发现吗啡耐受的大鼠对美沙酮和EKC无交叉耐受性,但美沙酮和EKC耐受的大鼠对吗啡有交叉耐受性。在本研究中,我们对美沙酮和EKC之间的交叉耐受性进行了特征描述。一组成年雌性Sprague-Dawley大鼠通过一系列自动静脉注射使其对美沙酮产生耐受性,第一天剂量为每2小时0.25mg/kg,第九天为每1.5小时2.0mg/kg。另一组大鼠以类似方式对EKC产生耐受性,第一天剂量为每2小时0.5mg/kg,第九天为每小时4mg/kg。美沙酮和EKC作用持续时间的缩短以及阿片类药物诱导的脑电图功率谱变化的减少,反映出对美沙酮和EKC的脑电图及行为效应产生了相对相似程度的耐受性发展。发现美沙酮耐受的大鼠对EKC的脑电图及行为效应有交叉耐受性,同样,EKC耐受的大鼠对美沙酮的也有交叉耐受性。因此,证明了μ受体激动剂和κ受体激动剂之间存在双向交叉耐受性。本研究结果与之前报道的结果共同表明,交叉耐受性可能与阿片类药物的受体选择性没有直接关系。这些阿片类药物不同的物理化学性质可能在交叉耐受性现象中起更决定性的作用。

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