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扩展获得可卡因和海洛因自我给药中的药物特异性。

Drug specificity in extended access cocaine and heroin self-administration.

机构信息

Behavioral Neuroscience Branch, National Institute on Drug Abuse-Intramural Research Program, NIH, Baltimore, MD, USA.

出版信息

Addict Biol. 2012 Nov;17(6):964-76. doi: 10.1111/j.1369-1600.2011.00385.x. Epub 2011 Oct 13.

DOI:10.1111/j.1369-1600.2011.00385.x
PMID:21995515
Abstract

Increased drug availability can precipitate a rapid escalation of drug consumption in both vulnerable humans and laboratory animals. Drug intake escalation is observed across a broad spectrum of drugs of abuse, including stimulants, opiates, ethanol and phencyclidine. Whether and to what extent the processes underlying escalated levels of drug intake vary across different substances is poorly understood. The present study sought to address this question in rats self-administering both cocaine and heroin-two addictive drugs with both common and different neurobiological effects. In experiment 1, we determined how cocaine intake is initially related to heroin intake in non-escalated rats with a limited access to both drugs. In experiment 2, two groups of rats were initially allowed to self-administer either cocaine or heroin for 1 hour per day and then after behavioral stabilization, for 6 hours per day to precipitate drug intake escalation. In each group, dose-injection functions for cocaine and heroin self-administration were generated. In experiment 1, regardless of the dose, rats with a high intake of one drug did not necessarily have a high intake of the alternate drug. In experiment 2, escalated levels of heroin or cocaine self-administration did not generalize to the other drug. This outcome was confirmed in a third drug substitution experiment following different access lengths to cocaine self-administration (i.e. 1, 4 and 8 hours). The processes underlying spontaneous and escalated drug overconsumption appear thus to vary across different drugs of abuse. More research should be devoted in the future to these differences.

摘要

药物供应的增加会促使脆弱的人类和实验室动物对药物的消费迅速升级。在广泛的滥用药物中,包括兴奋剂、阿片类药物、乙醇和苯环己哌啶,都观察到药物摄入升级的现象。在不同的物质中,导致药物摄入升级的过程是否以及在何种程度上有所不同,目前还知之甚少。本研究旨在解决这个问题,在可卡因和海洛因两种具有共同和不同神经生物学效应的成瘾性药物的自我给药大鼠中进行。在实验 1 中,我们确定了非升级大鼠在两种药物有限接触的情况下,可卡因的摄入量最初是如何与海洛因的摄入量相关的。在实验 2 中,两组大鼠最初每天允许自我注射可卡因或海洛因 1 小时,然后在行为稳定后,每天注射 6 小时,以引发药物摄入升级。在每组中,都生成了可卡因和海洛因自我给药的剂量-注射函数。在实验 1 中,无论剂量如何,一种药物摄入量高的大鼠并不一定对另一种药物有高摄入量。在实验 2 中,海洛因或可卡因自我给药水平的升级并没有推广到另一种药物。在不同的可卡因自我给药时间(即 1、4 和 8 小时)的第三个药物替代实验中,证实了这一结果。因此,自发和升级的药物过度消费的过程似乎因不同的滥用药物而有所不同。未来应该投入更多的研究来研究这些差异。

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