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[离子型谷氨酸受体通道阻滞剂对大鼠睡眠剥夺效应的作用]

[The action of ionotropic glutamate receptor channel blockers on effects of sleep deprivation in rats].

作者信息

Vataev S I, Oganesian G A, Lukomskaia N Ia, Magazanik L G

出版信息

Ross Fiziol Zh Im I M Sechenova. 2013 May;99(5):575-85.

Abstract

The action of non-competitive glutamate receptor antagonists on the effects of sleep deprivation has been studied on Krushinskii-Molodkina rats having an inherited predisposition to audiogenic seizures and Wistar rats deprived to this respond. Two types of glutamate receptor open channels blockers were used: the selective blockers of NMDA-receptors (memantine and IEM-1921) and blockers of mixed type, impacting both on the NMDA- and presumably Ca(2+)-permeable AMPA/kainate receptors (IEM-1754 and IEM 1925). Rats were subjected to 12 hours long sleep deprivation. Immediatly after that memantine and IEM-1921 were injected, and during the first 3 hours the total or partial reduction of fast-wave (paradoxical) sleep and a significant increase of the representation of wakefulness at the cost of reducing the total time of slow-wave sleep were observed. These effects are most likely to be a consequence of the blockade of NMDA-receptors functioning in the systems of the rat brain responsible for the launch and maintenance of fast-wave sleep. Injection of IEM-1754 and IEM-1925 on background of sleep deprivation did not affect the organization of sleep during the first 3 hours of their action. During the second three-hour period the rebound effect was observed. The obtained results indicate the involvement of NMDA glutamate receptors in the functioning of various parts of the sleep system of both rat lines.

摘要

在具有遗传性听源性癫痫易感性的克鲁申斯基-莫洛迪纳大鼠以及对此有反应的被剥夺睡眠的Wistar大鼠身上,研究了非竞争性谷氨酸受体拮抗剂对睡眠剥夺效应的作用。使用了两种类型的谷氨酸受体开放通道阻滞剂:NMDA受体的选择性阻滞剂(美金刚和IEM - 1921)以及混合型阻滞剂,其对NMDA受体和可能的Ca(2+)通透的AMPA/海人藻酸受体均有影响(IEM - 1754和IEM 1925)。大鼠经历了12小时的睡眠剥夺。之后立即注射美金刚和IEM - 1921,在最初3小时内观察到快速眼动(反常)睡眠的总量或部分减少,以及以慢波睡眠总时长减少为代价的清醒状态表现显著增加。这些效应很可能是大鼠大脑中负责启动和维持快速眼动睡眠的系统中NMDA受体功能被阻断的结果。在睡眠剥夺背景下注射IEM - 1754和IEM - 1925,在其作用的最初3小时内并未影响睡眠结构。在第二个三小时期间观察到了反弹效应。所得结果表明NMDA谷氨酸受体参与了两种大鼠品系睡眠系统各个部分的功能。

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