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N-甲基-D-天冬氨酸受体介导的钾离子外流与神经元凋亡。

NMDA receptor-mediated K+ efflux and neuronal apoptosis.

作者信息

Yu S P, Yeh C, Strasser U, Tian M, Choi D W

机构信息

Center for the Study of Nervous System Injury and Department of Neurology, Washington University School of Medicine, St. Louis, MO 63110, USA.

出版信息

Science. 1999 Apr 9;284(5412):336-9. doi: 10.1126/science.284.5412.336.

Abstract

Neuronal death induced by activating N-methyl-D-aspartate (NMDA) receptors has been linked to Ca2+ and Na+ influx through associated channels. Whole-cell recording from cultured mouse cortical neurons revealed a NMDA-evoked outward current, INMDA-K, carried by K+ efflux at membrane potentials positive to -86 millivolts. Cortical neurons exposed to NMDA in medium containing reduced Na+ and Ca2+ (as found in ischemic brain tissue) lost substantial intracellular K+ and underwent apoptosis. Both K+ loss and apoptosis were attenuated by increasing extracellular K+, even when voltage-gated Ca2+ channels were blocked. Thus NMDA receptor-mediated K+ efflux may contribute to neuronal apoptosis after brain ischemia.

摘要

通过激活N-甲基-D-天冬氨酸(NMDA)受体诱导的神经元死亡与Ca2+和Na+通过相关通道的内流有关。对培养的小鼠皮层神经元进行全细胞记录发现,在膜电位正向-86毫伏时,NMDA诱发的外向电流INMDA-K由K+外流携带。在含有减少的Na+和Ca2+(如在缺血脑组织中发现的)的培养基中暴露于NMDA的皮层神经元失去了大量细胞内K+并发生凋亡。即使电压门控Ca2+通道被阻断,增加细胞外K+也会减弱K+丢失和凋亡。因此,NMDA受体介导的K+外流可能在脑缺血后神经元凋亡中起作用。

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