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酸中毒、酸感应离子通道与神经元细胞死亡。

Acidosis, acid-sensing ion channels, and neuronal cell death.

机构信息

Neuroscience Division, Department of Biochemistry and Molecular Cell Biology, Institute of Medical Sciences, Shanghai Jiao Tong University School of Medicine, Shanghai 200025, China.

出版信息

Mol Neurobiol. 2011 Dec;44(3):350-8. doi: 10.1007/s12035-011-8204-2. Epub 2011 Sep 20.

Abstract

Acidosis is a common feature of many neuronal diseases and often accompanied with adverse consequences such as pain and neuronal injury. Before the discovery of acid-sensing ion channels (ASICs), protons were usually considered as a modulator of other ion channels, such as voltage-gated calcium channels, N-methyl-D-aspartate, and γ-amino butyric acid(A) receptor channels. Accordingly, the functional effects of acidosis were considered as consequences of modulations of these channels. Since the first cloning of ASICs in 1997, the conventional view on acidosis-mediated pain and cell injury has been dramatically changed. To date, ASICs, which are directly activated by extracellular protons, are shown to mediate most of the acidosis-associated physiological and pathological functions. For example, ASIC1a channels are reported to mediate acidosis-induced ischemic neuronal death. In this article, we will review the possible mechanisms that underlie ASIC1a channel-mediated neuronal death and discuss ASIC1a channel modulators involved in this process.

摘要

酸中毒是许多神经疾病的常见特征,常伴有疼痛和神经元损伤等不良后果。在酸感应离子通道(ASICs)被发现之前,质子通常被认为是其他离子通道(如电压门控钙通道、N-甲基-D-天冬氨酸和γ-氨基丁酸(A)受体通道)的调节剂。因此,酸中毒的功能效应被认为是这些通道调制的结果。自 1997 年首次克隆 ASICs 以来,人们对酸中毒介导的疼痛和细胞损伤的传统观点发生了巨大变化。迄今为止,直接被细胞外质子激活的 ASICs 被证明介导了大多数与酸中毒相关的生理和病理功能。例如,有报道称 ASIC1a 通道介导了酸中毒诱导的缺血性神经元死亡。在本文中,我们将综述 ASIC1a 通道介导的神经元死亡的可能机制,并讨论参与这一过程的 ASIC1a 通道调节剂。

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