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苯丙胺类似物对36秒固定比率强化程序的表现有不同影响。

Amphetamine analogs have differential effects on DRL 36-s schedule performance.

作者信息

Sabol K E, Richards J B, Layton K, Seiden L S

机构信息

University of Chicago, Department of Pharmacological and Physiological Sciences, IL 60637, USA.

出版信息

Psychopharmacology (Berl). 1995 Sep;121(1):57-65. doi: 10.1007/BF02245591.

DOI:10.1007/BF02245591
PMID:8539341
Abstract

Amphetamine and related compounds have previously been shown to differentially release dopamine (DA) and serotonin (5HT) in vivo and in vitro. The purpose of this report is directly to compare five amphetamine analogs on differential reinforcement of low rate 36-s (DRL 36-s) schedule performance, and to determine whether the reported increases in dopamine and/or serotonin release induced by these drugs can be related to observed behavioral differences. Amphetamine (AMPH) and methamphetamine (METH) induced large increases in response rate, methylenedioxymethamphetamine (MDMA) and para-chloroamphetamine (PCA) caused small increases in response rate, while fenfluramine (FEN) had no effect on response rate. AMPH, METH, PCA and MDMA caused a dose-dependent decrease in reinforcement rate, and FEN had no effect on reinforcement rate. AMPH, METH, and PCA but not FEN, shifted the peak of the inter-response time (IRT) distribution toward shorter intervals, MDMA decreased peak location only at the highest dose. All five drugs caused a dose-dependent decrease in peak area, indicating a loss of schedule control on the DRL 36-s schedule. Consistent with in vitro and in vivo release studies, the differential results of these five drugs on DRL 36-s schedule performance suggest a predominant dopamine role for AMPH and METH, a predominant serotonin role for FEN, and different degrees of combined dopaminergic and serotonergic roles for MDMA and PCA in the mediation of the task.

摘要

先前的研究表明,苯丙胺及相关化合物在体内和体外能不同程度地释放多巴胺(DA)和5-羟色胺(5HT)。本报告的目的是直接比较五种苯丙胺类似物对低速率36秒差异强化(DRL 36-s)程序表现的影响,并确定这些药物所报告的多巴胺和/或5-羟色胺释放增加是否与观察到的行为差异有关。苯丙胺(AMPH)和甲基苯丙胺(METH)使反应率大幅增加,亚甲二氧基甲基苯丙胺(MDMA)和对氯苯丙胺(PCA)使反应率小幅增加,而芬氟拉明(FEN)对反应率无影响。AMPH、METH、PCA和MDMA导致强化率呈剂量依赖性下降,FEN对强化率无影响。AMPH、METH和PCA(而非FEN)使反应间隔时间(IRT)分布的峰值向更短的间隔移动,MDMA仅在最高剂量时降低峰值位置。所有五种药物均导致峰值面积呈剂量依赖性下降,表明对DRL 36-s程序的程序控制丧失。与体外和体内释放研究一致,这五种药物对DRL 36-s程序表现的不同结果表明,在该任务的介导中,AMPH和METH主要作用于多巴胺,FEN主要作用于5-羟色胺,MDMA和PCA具有不同程度的多巴胺能和5-羟色胺能联合作用。

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