Then δ subunit of epithelial sodium channel in humans-a potential player in vascular physiology

被引:10
作者
Paudel, Puja [1 ,2 ]
McDonald, Fiona J. [1 ]
Fronius, Martin [1 ,2 ]
机构
[1] Univ Otago, Dept Physiol, Dunedin, New Zealand
[2] Univ Otago, HeartOtago, Dunedin, New Zealand
来源
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY | 2021年 / 320卷 / 02期
关键词
cardiovascular disease; ENaC; epithelial sodium channel; human vasculature; hypertension; subunits; NA+ CHANNEL; RESISTANT HYPERTENSION; FUNCTIONAL EXPRESSION; TISSUE DISTRIBUTION; GAMMA-SUBUNIT; BETA-SUBUNIT; EVANS BLUE; ENAC; PROTEINS; CLONING;
D O I
10.1152/ajpheart.00800.2020
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Vascular epithelial sodium channels (ENaCs) made up of canonical alpha, beta, and gamma subunits have attracted more attention recently owing to their physiological role in vascular health and disease. A fourth subunit, delta-ENaC, is expressed in various mammalian species, except mice and rats, which are common animal models for cardiovascular research. Accordingly, delta-ENaC is the least understood subunit. However, the recent discovery of delta subunit in human vascular cells indicates that this subunit may play a significant role in normal/pathological vascular physiology in humans. Channels containing the delta subunit have different biophysical and pharmacological properties compared with channels containing the a subunit, with the potential to alter the vascular function of ENaC in health and disease. Hence, it is important to investigate the expression and function of delta-ENaC in the vasculature to identify whether delta-ENaC is a potential new drug target for the treatment of cardiovascular disease. In this review, we will focus on the existing knowledge of delta-ENaC and implications for vascular physiology and pathophysiology in humans.
引用
收藏
页码:H487 / H493
页数:7
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