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可卡因与(+)-AJ76或氯氮平联合使用时的强化和辨别刺激效应评估。

Evaluation of the reinforcing and discriminative stimulus effects of cocaine in combination with (+)-AJ76 or clozapine.

作者信息

Vanover K E, Piercey M F, Woolverton W L

机构信息

Drug Abuse Research Center, University of Chicago, Pritzker School of Medicine, Illinois.

出版信息

J Pharmacol Exp Ther. 1993 Aug;266(2):780-9.

PMID:8355207
Abstract

Because self-administration and discrimination of a drug by animals correlate with its abuse and subjective effects in humans, interventions that modify the reinforcing and discriminative stimulus effects of the drug may be useful in the treatment of its abuse. The present study was designed to evaluate the effects of the putative dopamine autoreceptor antagonist (+)-AJ76 (AJ) or the atypical antipsychotic clozapine (CLZ) on the reinforcing and discriminative stimulus effects of cocaine in monkeys. One group of rhesus monkeys (n = 6) was allowed to self-administer cocaine (0.03 or 0.1 mg/kg/injection i.v. fixed-ratio 10, 2 hr/day). A second group of monkeys (n = 5) was trained to discriminate cocaine (0.2 or 0.4 mg/kg i.m., 10 min presession) from saline in a two lever, food-reinforced, drug discrimination paradigm. When behavior was stable, AJ or CLZ was administered i.m., 15 or 30 min presession. Intermediate doses of both compounds (1.0-3.0 mg/kg of AJ; 0.3-1.0 mg/kg of CLZ) increased cocaine self-administration, while responding remained evenly distributed over the session. A higher dose of CLZ decreased cocaine self-administration in an apparently nonspecific manner. When combined with saline, partial substitution for cocaine was seen in one of three monkeys with AJ and in none with CLZ. In combination with the training dose of cocaine in the discrimination experiment, both AJ and CLZ decreased drug appropriate responding by at least 50% in two of four monkeys, but had little or no effect in the other monkeys up to doses that completely suppressed lever pressing (6.4 mg/kg of AJ; 3.2 mg/kg of CLZ). Taken together, the present findings suggest that any blockade of the reinforcing and discriminative stimulus effects of cocaine by AJ and CLZ was, at best, partial. Furthermore, the stimulant effects of AJ observed in rats were not prominent in monkeys.

摘要

由于动物对药物的自我给药和辨别能力与该药物在人类中的滥用情况及其主观效应相关,因此,改变药物强化和辨别刺激效应的干预措施可能对治疗药物滥用有用。本研究旨在评估假定的多巴胺自身受体拮抗剂(+)-AJ76(AJ)或非典型抗精神病药物氯氮平(CLZ)对猴子可卡因强化和辨别刺激效应的影响。一组恒河猴(n = 6)被允许自我给药可卡因(0.03或0.1 mg/kg/注射,静脉注射,固定比率10,每天2小时)。第二组猴子(n = 5)在双杠杆、食物强化的药物辨别范式中接受训练,以辨别可卡因(0.2或0.4 mg/kg,肌肉注射,实验前10分钟)和生理盐水。当行为稳定后,在实验前15或30分钟肌肉注射AJ或CLZ。两种化合物的中等剂量(AJ为1.0 - 3.0 mg/kg;CLZ为0.3 - 1.0 mg/kg)增加了可卡因的自我给药量,而反应在整个实验过程中仍均匀分布。较高剂量的CLZ以一种明显非特异性的方式减少了可卡因的自我给药量。当与生理盐水联合使用时,三只猴子中有一只出现了用AJ部分替代可卡因的情况,而用CLZ则未出现这种情况。在辨别实验中,与可卡因训练剂量联合使用时,AJ和CLZ在四只猴子中有两只使药物适当反应减少了至少50%,但在其他猴子中,直至完全抑制杠杆按压的剂量(AJ为6.4 mg/kg;CLZ为3.2 mg/kg),其影响很小或没有影响。综上所述,目前的研究结果表明,AJ和CLZ对可卡因强化和辨别刺激效应的任何阻断作用充其量只是部分性的。此外,AJ在大鼠中观察到的兴奋作用在猴子中并不显著。

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