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恒河猴对可卡因-海洛因混合物的自我给药:纳曲酮的拮抗作用。

Self-administration of cocaine-heroin combinations by rhesus monkeys: antagonism by naltrexone.

作者信息

Rowlett J K, Wilcox K M, Woolverton W L

机构信息

Department of Psychiatry and Human Behavior, University of Mississippi Medical Center, Jackson, USA.

出版信息

J Pharmacol Exp Ther. 1998 Jul;286(1):61-9.

PMID:9655842
Abstract

Low, nonreinforcing doses of heroin have been shown to shift the dose-response function of cocaine leftward in rhesus monkeys trained under a progressive-ratio schedule of i.v. drug injection. Our study sought to determine 1) whether a reciprocal enhancement of heroin self-administration would be observed when heroin was combined with low, nonreinforcing doses of cocaine, and 2) whether self-administration of cocaine-heroin combinations could be antagonized by the opioid antagonist naltrexone. Rhesus monkeys (n = 4) were prepared with i.v. catheters and trained to self-administer cocaine under a progressive-ratio schedule. The initial response requirement of this schedule was fixed-ratio 120, which doubled across the session to a maximum of 1920. Injections were separated by a 30-min time out. Cocaine dose-response functions (6.4-100 micrograms/kg/injection) for injections/session and breakpoints were monophasic, i.e., increased with dose until responding reached a maximum. Heroin dose-response functions (1.6-25 micrograms/kg/ injection) either increased to a peak and then decreased or reached an asymptote. When nonreinforcing doses of cocaine (3.2-25 micrograms/kg/injection) were combined with heroin, the heroin dose-response function was shifted to the left, without change in maximum injections/session. Pressession treatments with naltrexone (3.2-1600 micrograms/kg, i.m., 10-min presession) antagonized self-administration of heroin and heroin + cocaine combinations in a dose-dependent fashion. However, naltrexone treatment had no effect on cocaine self-administration. Antagonism by naltrexone of self-administration of heroin and heroin + cocaine was surmounted by increasing the dose of heroin either alone or in the heroin + cocaine combination. In vivo apparent pA2 and pKB analyses of these data revealed values of approximately 8.0, consistent with a role for mu opioid receptors in the self-administration of heroin and cocaine-heroin (i.e., "speedball") combinations.

摘要

在静脉注射药物的累进比率时间表训练下的恒河猴中,低剂量、无强化作用的海洛因已被证明可使可卡因的剂量-反应函数向左移动。我们的研究旨在确定:1)当海洛因与低剂量、无强化作用的可卡因联合使用时,是否会观察到海洛因自我给药的相互增强;2)阿片类拮抗剂纳曲酮是否能拮抗可卡因-海洛因组合的自我给药。给4只恒河猴植入静脉导管,并在累进比率时间表下训练其自我给药可卡因。该时间表的初始反应要求为固定比率120,在整个实验过程中翻倍至最大值1920。注射间隔为30分钟的暂停期。每次注射/实验时段的可卡因剂量-反应函数(6.4-100微克/千克/注射)和断点呈单相,即随着剂量增加直至反应达到最大值。海洛因剂量-反应函数(1.6-25微克/千克/注射)要么先增加到峰值然后下降,要么达到渐近线。当无强化作用的可卡因剂量(3.2-25微克/千克/注射)与海洛因联合使用时,海洛因剂量-反应函数向左移动,每次实验时段的最大注射量不变。纳曲酮(3.2-1600微克/千克,肌肉注射,实验前10分钟)的预处理以剂量依赖的方式拮抗海洛因和海洛因+可卡因组合的自我给药。然而,纳曲酮治疗对可卡因自我给药没有影响。通过单独增加海洛因剂量或增加海洛因+可卡因组合中的海洛因剂量,可以克服纳曲酮对海洛因和海洛因+可卡因自我给药的拮抗作用。对这些数据进行体内表观pA2和pKB分析,得出的值约为8.0,这与μ阿片受体在海洛因和可卡因-海洛因(即“速球”)组合自我给药中的作用一致。

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