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药物对反应持续时间分化的影响。VI:低反应率强化程序下的差异效应。

Effects of drugs on response duration differentiation. VI: differential effects under differential reinforcement of low rates of responding schedules.

作者信息

McClure G Y, McMillan D E

机构信息

Department of Pharmacology and Toxicology, University of Arkansas for Medical Sciences, Little Rock 72205, USA.

出版信息

J Pharmacol Exp Ther. 1997 Jun;281(3):1368-80.

PMID:9190873
Abstract

The effects of methamphetamine, phencyclidine and delta9-tetrahydrocannabinol on responding under differential reinforcement of low rate schedules (DRL schedules) were studied under three different DRL time requirements. Under the DRL schedules studied, rats were required to space responses at least a minimum, but not more than a maximum, time interval apart. The time intervals between responses (interresponse times, or IRTs), when plotted as a frequency distribution, were usually a normal distribution with the peak at or near the minimum IRT required for delivery of the reinforcer. Methamphetamine flattened the IRT distribution and increased the frequency of long pauses under the DRL 1-1.3 sec schedule, but shifted the IRT distribution toward shorter IRTs under the DRL 4-5.2 and 10-13 sec schedules. Under the DRL 1-1.3 sec schedule, phencyclidine also increased long pauses. Under the DRL 4-5.2 sec and 10-13 sec schedules, phencyclidine produced dual effects on the IRT relative frequency distributions producing increases in the proportion of short IRTs similar to methamphetamine at low doses, but higher doses increased long pauses as well. delta9-Tetrahydrocannabinol had little effect on responding under the DRL 1-1.3 sec and DRL 4-5.2 sec schedules, but it greatly increased the relative frequency of short IRTs under the DRL 10-13 sec schedule. Thus the effects of drugs on responding under these DRL schedules depended on the drug, the dose and the time requirements of the schedule, which suggests that a simple description of the effects of drugs on timing behavior or time perception is inadequate.

摘要

研究了甲基苯丙胺、苯环利定和δ9-四氢大麻酚在三种不同的低比率强化程序(DRL程序)下对反应的影响。在所研究的DRL程序中,要求大鼠将反应间隔至少保持在一个最短但不超过最长的时间间隔。当将反应之间的时间间隔(反应间隔时间,或IRT)绘制成频率分布时,通常呈正态分布,峰值位于或接近强化物发放所需的最短IRT处。甲基苯丙胺使IRT分布变平,并在DRL 1 - 1.3秒程序下增加了长停顿的频率,但在DRL 4 - 5.2秒和10 - 13秒程序下使IRT分布向更短的IRT偏移。在DRL 1 - 1.3秒程序下,苯环利定也增加了长停顿。在DRL 4 - 5.2秒和10 - 13秒程序下,苯环利定对IRT相对频率分布产生双重影响,在低剂量时产生类似于甲基苯丙胺的短IRT比例增加,但高剂量时也增加了长停顿。δ9-四氢大麻酚在DRL 1 - 1.3秒和DRL 4 - 5.2秒程序下对反应影响很小,但在DRL 10 - 13秒程序下大大增加了短IRT的相对频率。因此,药物在这些DRL程序下对反应的影响取决于药物、剂量和程序的时间要求,这表明对药物对定时行为或时间感知影响的简单描述是不够的。

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