Circadian clocks regulate cardiac arrhythmia susceptibility, repolarization, and ion channels

被引:9
作者
Delisle, Brian P. [1 ]
Stumpf, John L. [1 ]
Wayland, Jennifer L. [1 ]
Johnson, Sidney R. [1 ]
Ono, Makoto [1 ]
Hall, Dalton [1 ]
Burgess, Don E. [1 ,2 ]
Schroder, Elizabeth A. [1 ,3 ]
机构
[1] Univ Kentucky, Dept Physiol, 800 Rose St,MS508, Lexington, KY 40536 USA
[2] Asbury Univ, Dept Sci & Hlth, One Macklem Dr, Wilmore, KY 40390 USA
[3] Univ Kentucky, Dept Internal Med, Div Pulm Crit Care & Sleep Med, 740 S Limestone St,L543, Lexington, KY 40536 USA
关键词
CARDIOMYOCYTE MOLECULAR CLOCK; Q-T INTERVAL; BLOOD-PRESSURE; E-BOX; CARDIOVASCULAR-DISEASE; DBP TRANSCRIPTION; GENE-EXPRESSION; MOUSE MODELS; STROKE ONSET; HEART;
D O I
10.1016/j.coph.2020.09.015
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Daily changes in the incidence of sudden cardiac death (SCD) reveal an interaction between environmental rhythms and internal circadian rhythms. Circadian rhythms are physiological rhythms that alter physiology to anticipate daily changes in the environment. They reflect coordinated activity of cellular circadian clocks that exist throughout the body. This review provides an overview of the state of the field by summarizing the results of several different transgenic mouse models that disrupt the function of circadian clocks throughout the body, in cardiomyocytes, or in adult cardiomyocytes. These studies identify important roles for circadian clocks in regulating heart rate, ventricular repolarization, arrhythmogenesis, and the functional expression of cardiac ion channels. They highlight a new dimension in the regulation of cardiac excitability and represent initial forays into understanding the complexities of how time impacts the functional regulation of ion channels, cardiac excitability, and time of day changes in the incidence of SCD.
引用
收藏
页码:13 / 20
页数:8
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