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电压门控钠通道的pH调节

pH Modulation of Voltage-Gated Sodium Channels.

作者信息

Peters Colin H, Ghovanloo Mohammad-Reza, Gershome Cynthia, Ruben Peter C

机构信息

Department of Biomedical Physiology and Kinesiology, Simon Fraser University, Burnaby, BC, Canada.

出版信息

Handb Exp Pharmacol. 2018;246:147-160. doi: 10.1007/164_2018_99.

Abstract

Changes in blood and tissue pH accompany physiological and pathophysiological conditions including exercise, cardiac ischemia, ischemic stroke, and cocaine ingestion. These conditions are known to trigger the symptoms of electrical diseases in patients carrying sodium channel mutations. Protons cause a diverse set of changes to sodium channel gating, which generally lead to decreases in the amplitude of the transient sodium current and increases in the fraction of non-inactivating channels that pass persistent currents. These effects are shared with disease-causing mutants in neuronal, skeletal muscle, and cardiac tissue and may be compounded in mutants that impart greater proton sensitivity to sodium channels, suggesting a role of protons in triggering acute symptoms of electrical disease.In this chapter, we review the mechanisms of proton block of the sodium channel pore and a suggested mode of action by which protons alter channel gating. We discuss the available data on isoform specificity of proton effects and tissue level effects. Finally, we review the role that protons play in disease and our own recent studies on proton-sensitizing mutants in cardiac and skeletal muscle sodium channels.

摘要

血液和组织pH值的变化伴随着包括运动、心脏缺血、缺血性中风和可卡因摄入在内的生理和病理生理状况。已知这些状况会在携带钠通道突变的患者中引发电疾病症状。质子会使钠通道门控发生多种变化,通常会导致瞬时钠电流幅度降低以及通过持续电流的非失活通道比例增加。这些效应在神经元、骨骼肌和心脏组织中的致病突变体中也存在,并且在赋予钠通道更高质子敏感性的突变体中可能会更加复杂,这表明质子在引发电疾病急性症状中发挥作用。在本章中,我们回顾了质子对钠通道孔的阻断机制以及质子改变通道门控的一种推测作用模式。我们讨论了关于质子效应的同工型特异性和组织水平效应的现有数据。最后,我们回顾了质子在疾病中的作用以及我们自己最近关于心脏和骨骼肌钠通道中质子敏感突变体的研究。

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