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一种GABAC受体拮抗剂对大鼠睡眠-觉醒行为的研究。

Study of a GABAC receptor antagonist on sleep-waking behavior in rats.

作者信息

Arnaud C, Gauthier P, Gottesmann C

机构信息

Laboratoire de Psychophysiologie, Faculté des Sciences, Université de Nice-Sophia Antipolis, 06108 Nice, France.

出版信息

Psychopharmacology (Berl). 2001 Apr;154(4):415-9. doi: 10.1007/s002130000653.

Abstract

RATIONALE

gamma-Aminobutyric acid (GABA) is the main inhibitory transmitter of the brain. The involvement of GABAA and GABAB receptors in sleep-waking processes is well established.

OBJECTIVES

This research studied the influence of GABAC receptors.

METHODS

The rats were randomly infused in the fourth ventricle with vehicle and 25, 50, and 100 micrograms (1,2,5,6,-tetrahydropyridine)-methylphosphinic acid (TPMPA), a specific antagonist of GABAC receptors.

RESULTS

Principally at 50 micrograms, the molecule induced an increase of waking from 44.7% to 61.7% (P < 0.003), which was the consequence of enhancement of both active and quiet wakefulness. Total slow wave sleep was decreased, particularly the slow-wave stage from 39% to 27.7% (P < 0.02). Paradoxical sleep was also decreased from 14.5% to 9.1% (P < 0.01).

CONCLUSIONS

GABAC receptors are also involved in sleep-waking regulation. Since the sensitivity of GABAC receptors to GABA is much higher than that of GABAA and GABAB receptors, GABAC receptor modulators could be potential medications acting at low doses with fewer side effects.

摘要

原理

γ-氨基丁酸(GABA)是大脑主要的抑制性神经递质。GABAA和GABAB受体参与睡眠-觉醒过程已得到充分证实。

目的

本研究探讨GABAC受体的影响。

方法

将大鼠随机经第四脑室注入溶剂以及25、50和100微克的(1,2,5,6-四氢吡啶)-甲基次膦酸(TPMPA),后者是GABAC受体的特异性拮抗剂。

结果

主要在剂量为50微克时,该分子使清醒时间从44.7%增加至61.7%(P<0.003),这是主动和安静觉醒均增强的结果。总慢波睡眠减少,尤其是慢波阶段从39%降至27.7%(P<0.02)。异相睡眠也从14.5%降至9.1%(P<0.01)。

结论

GABAC受体也参与睡眠-觉醒调节。由于GABAC受体对GABA的敏感性远高于GABAA和GABAB受体,GABAC受体调节剂可能是低剂量、副作用少的潜在药物。

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