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慢性抗抑郁药对大鼠焦虑操作性冲突程序的影响。

Effects of chronic antidepressants in an operant conflict procedure of anxiety in the rat.

作者信息

Beaufour C C, Ballon N, Le Bihan C, Hamon M, Thiébot M H

机构信息

INSERM U.288, Faculty of Medicine Pitié-Salpêtrière, Paris, France.

出版信息

Pharmacol Biochem Behav. 1999 Apr;62(4):591-9. doi: 10.1016/s0091-3057(98)00180-4.

Abstract

The effects of chronic antidepressants were investigated in an animal procedure for the study of anxiety and anxiolytics, the conditioned suppression of operant behavior in rats. In daily 18-min sessions, three periods of nonpunished lever pressing for food alternated with two 4-min periods signaled by a light-on conditioned stimulus during which 50% of the responses were randomly punished by electric foot shocks. Antidepressants were administered once daily for 7-8 weeks to trained, food-restricted rats. Desipramine (dose regimen increase from 4 to 16 mg/kg/day) induced a gradual (4-5-week latency) release of response suppression during punished periods over the course of several weeks of testing. This anxiolytic-like effect was still present 3 weeks following drug discontinuation. In contrast, chronic imipramine (dose regimen increase from 4 to 16 mg/kg/day), maprotiline (4 to 16 mg/kg/day), phenelzine (2 to 4 mg/kg/day), and fluoxetine (1 or 8 mg/kg/day; constant dose), resulted in no change in punished responding, suggesting that no anxiolytic-like effect developed in the course of chronic treatment with these compounds. The largest dose of all antidepressants studied (except fluoxetine) induced a moderate to marked reduction of nonpunished performance that disappeared within 1 week after the last injection. A transient release of conditioned response suppression emerged during the week that followed discontinuation of imipramine, maprotiline, and fluoxetine (8 mg/kg/day). This apparent anxiolytic-like activity might be due to a reduction of some adverse effect induced by the high doses used, and/or might have resulted from a new dynamic equilibrium between monoamine release, reuptake processes, and sensitivity of postsynaptic receptors. In conclusion, operant conflict procedures in rats seem not particularly able to model human anxiety sensitive to chronic antidepressant treatments.

摘要

在一项用于研究焦虑和抗焦虑药的动物实验程序(即大鼠操作性行为的条件性抑制)中,对慢性抗抑郁药的效果进行了研究。在每天18分钟的实验时段里,三个无惩罚的压杆获取食物时段与两个4分钟时段交替出现,这两个4分钟时段由灯光开启的条件刺激信号指示,在此期间,50%的反应会被随机给予足部电击惩罚。对经过训练且限制食物摄入的大鼠每天给药一次抗抑郁药,持续7 - 8周。地昔帕明(剂量方案从4毫克/千克/天增加到16毫克/千克/天)在数周的测试过程中,诱导出在惩罚时段反应抑制的逐渐(4 - 5周潜伏期)解除。这种抗焦虑样效应在停药3周后仍然存在。相比之下,慢性给予丙咪嗪(剂量方案从4毫克/千克/天增加到16毫克/千克/天)、马普替林(4毫克/千克/天至16毫克/千克/天)、苯乙肼(2毫克/千克/天至4毫克/千克/天)和氟西汀(1毫克/千克/天或8毫克/千克/天;固定剂量),惩罚反应没有变化,这表明用这些化合物进行慢性治疗过程中未产生抗焦虑样效应。所研究的所有抗抑郁药(氟西汀除外)的最大剂量诱导出非惩罚性表现的中度至显著降低,这种降低在最后一次注射后1周内消失。在停用丙咪嗪、马普替林和氟西汀(8毫克/千克/天)后的一周内出现了条件反应抑制的短暂解除。这种明显的抗焦虑样活性可能是由于所用高剂量诱导的某些不良反应的减轻,和/或可能是由于单胺释放、再摄取过程以及突触后受体敏感性之间新的动态平衡所致。总之,大鼠的操作性冲突程序似乎不太能够模拟对慢性抗抑郁药治疗敏感的人类焦虑。

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