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向梅纳特基底核微量注射卡巴胆碱所诱导的去同步化(快速眼动)睡眠抑制是由谷氨酸能系统介导的。

Desynchronized (REM) sleep inhibition induced by carbachol microinjections into the nucleus basalis of Meynert is mediated by the glutamatergic system.

作者信息

Manfridi A, Mancia M

机构信息

Istituto Fisiologia Umana II, Universita' degli Studi di Milano, Italy.

出版信息

Exp Brain Res. 1996 Apr;109(1):174-8. doi: 10.1007/BF00228641.

Abstract

The aim of this paper was to study the effects of microinjections of carbachol, a mixed cholinergic agonist, into the nucleus basalis of Meynert (NBM) of rats on the wake-sleep cycle. Carbachol (2.74 nmol) was able to increase wakefulness (W) and decrease desynchronized sleep (DS). To verify the hypothesis that the effects of carbachol are at least partially mediated by the glutamatergic system, the NMDA antagonist 2-amino-5-phosphonopentanoic acid and the non-NMDA antagonist D-gamma-glutamylaminomethanesulfonic acid were injected into the NBM before carbachol. Pretreatment with these glutamate receptor antagonists counteracted the effect of carbachol on DS. The effect of carbachol on W was not modified by the pretreatment with the glutamate receptor antagonists. This is the first study showing that carbachol injected into the NBM increases W and decreases spontaneous DS in the rat. Moreover, our results tend to indicate that the decrease in DS following the injection of carbachol into the NBM is related to the release of endogenous glutamate.

摘要

本文旨在研究向大鼠Meynert基底核(NBM)微量注射混合胆碱能激动剂卡巴胆碱对觉醒-睡眠周期的影响。卡巴胆碱(2.74纳摩尔)能够增加觉醒(W)并减少去同步化睡眠(DS)。为了验证卡巴胆碱的作用至少部分是由谷氨酸能系统介导的这一假设,在注射卡巴胆碱之前,将N-甲基-D-天冬氨酸(NMDA)拮抗剂2-氨基-5-膦酰戊酸和非NMDA拮抗剂D-γ-谷氨酰氨基甲磺酸注入NBM。用这些谷氨酸受体拮抗剂进行预处理可抵消卡巴胆碱对DS的作用。谷氨酸受体拮抗剂预处理并未改变卡巴胆碱对W的作用。这是第一项表明向NBM注射卡巴胆碱可增加大鼠W并减少自发性DS的研究。此外,我们的结果倾向于表明,向NBM注射卡巴胆碱后DS的减少与内源性谷氨酸的释放有关。

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