Possible Involvement of TRP Channels in Cardiac Hypertrophy and Arrhythmia

被引:1
作者
Watanabe, Hiroyuki [1 ]
Iino, Kenji [1 ]
Ohba, Takayoshi [1 ,2 ]
Ito, Hiroshi
机构
[1] Akita Univ, Grad Sch Med, Dept Cardiovasc & Resp Med, Akita 0108543, Japan
[2] Akita Univ, Grad Sch Med, Dept Physiol, Akita 0108543, Japan
关键词
Cardiac arrhythmia; cardiac hypertrophy; Orai1; Stim1; TRPC1; TRPC3; TRPC6; TRPM4; NONSELECTIVE CATION CHANNEL; OPERATED CA2+ ENTRY; RECEPTOR POTENTIAL CHANNELS; FUNCTIONAL-CHARACTERIZATION; ATRIAL-FIBRILLATION; CHLORIDE CURRENT; NUCLEAR FACTOR; ION-CHANNEL; CALCINEURIN; HEART;
D O I
暂无
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Over the past 20 years, studies of transient receptor potential (TRP) channels have significantly extended our knowledge regarding the molecular basis of Ca2+ signals in cardiac myocytes. The functional significance of cardiac TRP channels is likely connected to the alteration of membrane potential or Ca2+ entry into a noncontractile compartment, where gene expression responsible for various cardiac diseases is induced. This review highlights some aspects of TRP channels with anticipated roles in cardiac disease. Evidence suggests that (a) increased activities of TRPC1, TRPC3, or TRPC6 are involved in the development of cardiac hypertrophy, where these TRPC channels act as unique sensors for a wide range of hypertrophic stimuli, and (b) mutations in TRPM4 are now recognized as causes of human cardiac conduction disorders. Ultimately, TRP channels may become novel pharmacological targets in the treatment of human cardiac disease.
引用
收藏
页码:283 / 294
页数:12
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