摘要
酸敏感离子通道(ASICs)属于上皮Na^+通道/退化蛋白超家族,对细胞外H^+浓度变化敏感,其受多种外源性配体调控,产生不同生理和病理学效应。越来越多研究发现,ASICs参与脑缺血、炎症、肿瘤等具有酸化改变的病理过程。简介ASICs的结构及其配体作用位点以及各亚基的组织分布和电生理特性,主要对各类ASICs外源性配体的研究进展作一综述。
Acid-sensing ion channels(ASICs) belong to the epithelial Na+-channels(ENa C)/degenerin(DEG) family, which are activated by extracellular acidosis and regulated by a variety of exogenous ligands, leading to different physiological and pathological consequences. Recent studies have demonstrated that ASICs are involved in cerebral ischemia, infl ammation, tumor, and other pathological processes associated with extracellular acidification. In this paper, the structure of ASICs and action sites of their exogenous ligands as well as the tissue distributions and electrophysiological characteristics of the subunits were introduced, and the research progress on various types of the exogenous ligands of ASICs was emphatically reviewed.
出处
《药学进展》
CAS
2016年第11期865-870,共6页
Progress in Pharmaceutical Sciences
基金
国家自然科学基金(No.81101372
No.81270011)
关键词
酸敏感离子通道
外源性配体
调节作用
acid-sensing ion channel
exogenous ligand
regulatory effect