吗啡和氯丙嗪对穿梭箱条件回避反应获得的急性影响。

A M Ageel, L Chin, C L Trafton, B C Jones, A L Picchioni
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引用次数: 8

摘要

在大规模试验条件回避反应(CAR)试验开始前30 min,给药硫酸吗啡0.25 ~ 24.0 mg/kg或盐酸氯丙嗪0.0625 ~ 4.0mg/kg。两种药物的分级剂量分别应用于三个CAR任务难度水平,这些难度水平是由条件刺激和非条件刺激的持续时间、试验间隔和电击强度的操纵产生的。氯丙嗪以剂量相关的方式导致所有任务中CAR获得的减少。相比之下,吗啡产生了双相剂量反应。对于给定的任务难度,低剂量吗啡增强习得,而高剂量吗啡抑制习得。随着任务难度的增加,需要相对较大剂量的吗啡来抑制或促进CAR的获得。这些结果强调,不仅需要考虑药物剂量水平,还需要考虑任务难度在药物应用学习范式中的相互作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Acute effects of morphine and chlorpromazine on the acquisition of shuttle box conditioned avoidance response.

Morphine sulfate, 0.25-24.0 mg/kg, or chlorpromazine hydrochloride, 0.0625-4.0mg/kg were administered subcutaneously to naive rats 30 min prior to the start of massed-trials conditioned avoidance response (CAR) testing. The graded doses of both drugs were applied in each of three CAR task difficulty levels created by manipulation of the duration of conditioned and unconditioned stimuli, intertrial interval and shock intensity. Chlorpromazine, in a dose-related manner, caused a decrement in CAR acquisition in all tasks. Morphine, in comparison, produced a biphasic dose response. For a given task difficulty, low doses of morphine enhanced acquisition, whereas higher doses inhibited acquisition. With increasing task difficulty, relatively larger doses of morphine were required to inhibit or facilitate acquisition of CAR. These results emphasize the need to consider not only drug dosage levels, but also the interaction of task difficulty in the application of drugs in learning paradigms.

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