arrhythmia;
hERG;
I-Kr;
I-Ks;
KCNE1;
KCNE2;
KCNQ1;
long QT syndrome;
D O I:
10.1016/j.vph.2005.07.013
中图分类号:
R9 [药学];
学科分类号:
1007 ;
摘要:
Ion channels control electrical excitability in living cells. In mammalian heart, the opposing actions of Na+ and Ca2+ ion influx, and K+ ion efflux, through cardiac ion channels determine the morphology and duration of action potentials in cardiac myocytes, thus controlling the heartbeat. The last decade has seen a leap in our understanding of the molecular genetic origins of inherited cardiac arrhythmia, largely through identification of mutations in cardiac ion channels and the proteins that regulate them. Further, recent advances have shown that 'acquired arrhythmias', which occur more commonly than inherited arrhythmias, arise due to a variety of environmental factors including side effects of therapeutic drugs and often have a significant genetic component. Here, we review the pharmacogenetics of cardiac ion channels-the interplay between genetic and pharmacological factors that underlie human cardiac arrhythmias. (c) 2005 Elsevier Inc. All rights reserved.
机构:
Uniformed Serv Univ Hlth Sci, Dept Anat Physiol & Genet, Bethesda, MD 20814 USAWashington Univ, Sch Med, Dept Cell Biol & Physiol, St Louis, MO 63110 USA
Flagg, Thomas P.
Nichols, Colin G.
论文数: 0引用数: 0
h-index: 0
机构:
Washington Univ, Sch Med, Dept Cell Biol & Physiol, St Louis, MO 63110 USAWashington Univ, Sch Med, Dept Cell Biol & Physiol, St Louis, MO 63110 USA
Nichols, Colin G.
CIRCULATION-ARRHYTHMIA AND ELECTROPHYSIOLOGY,
2011,
4
(06):
: 796
-
798