期刊
PROGRESS IN BIOPHYSICS & MOLECULAR BIOLOGY
卷 98, 期 2-3, 页码 347-362出版社
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.pbiomolbio.2009.01.002
关键词
Kv11.1; Arrhythmia; Pharmacological treatment; Repolarisation reserve; Triggered activity; Fibrillation
资金
- Danish National Research Foundation Centre
- Novo Nordisk Foudation
- Aase and Ejnar Danielsen Foundation
- National Danish Research Council
The cardiac action potential is the result Of all orchestrated function of a number of different ion channels. Action potential repolarisation in humans relies on three potassium current components named I-Kr, I-Ks and I-K1 with party overlapping functions. The ion channel alpha-subunits conducting these currents are hERG1 (Kv11.1), KCNQ1 (Kv7.1) and Kir2.1. Loss-of-function in any of these currents call result in long QT syndrome. Long QT is a pro-arrhythmic disease with increased risk of developing lethal ventricular arrhythmias Such as Torsade de Pointes and ventricular fibrillation. In addition to congenital long QT, acquired long QT can also constitute a safety risk. Especially unintended inhibition of the hERG1 channel constitutes a major concern in the development of new drugs. Based oil this knowledge is has been speculated whether activation of the hERG1 channel could be anti-arrhythmic and thereby constitute a new principle in treatment of cardiac arrhythmogenic disorders. The first hERG1 channel agonist was reported in 2005 and a limited number of such compounds are now available. In the present text we review results obtained by hERG1 channel activation in a number of cardiac relevant settings from in vitro to in vivo. It is demonstrated how the principle of hERG1 channel activation Under certain circumstances can constitute a new anti-arrhythmogenic principle. Finally, important conceptual differences between the short QT syndrome and the hERG1 channel activation. are evaluated. (C) 2009 Elsevier Ltd. All rights reserved,
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