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神经递质、药物及化学修饰对NMDA受体反应性的调节

Modulation of NMDA receptor responsiveness by neurotransmitters, drugs and chemical modification.

作者信息

Reynolds I J

机构信息

Department of Pharmacology, University of Pittsburgh, PA 15261.

出版信息

Life Sci. 1990;47(20):1785-92. doi: 10.1016/0024-3205(90)90280-5.

Abstract

The NMDA receptor is intimately involved an a wide range of pathophysiological processes in the mammalian brain, including epilepsy and ischemia-induced neurodegeneration. The widespread distribution of NMDA receptors places almost every area of the brain at risk from NMDA receptor over-activity. However, it is clear that the central nervous system can function effectively without imminent danger of self-destruction. The focus of this review is the processes that control NMDA receptor responsiveness in vivo. The review will cover the modulation of the receptor by Mg2+, glycine, Zn2+ and polyamines that is believed to occur by virtue of interaction with distinct ligand binding sites on the NMDA receptor complex. Studies suggesting a role for receptor phosphorylation and for redox modulation will be discussed. Finally, some evidence for indirect regulation of cellular responses to NMDA receptor activation by other neurotransmitters will be presented.

摘要

NMDA受体密切参与哺乳动物大脑中的多种病理生理过程,包括癫痫和缺血性神经退行性变。NMDA受体的广泛分布使大脑的几乎每个区域都面临NMDA受体过度激活的风险。然而,很明显中枢神经系统能够有效发挥功能而没有立即自我毁灭的危险。本综述的重点是体内控制NMDA受体反应性的过程。该综述将涵盖Mg2+、甘氨酸、Zn2+和多胺对受体的调节,据信这些调节是通过与NMDA受体复合物上不同的配体结合位点相互作用而发生的。将讨论提示受体磷酸化和氧化还原调节作用的研究。最后,将介绍一些其他神经递质对NMDA受体激活的细胞反应进行间接调节的证据。

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