Pacemaker channels play a major role in the generation of sinoatrial rhythmic activity. However, their expression is not confined to specialized myocardial cells, such as primary and subsidiary pacemakers. Electrophysiological and molecular data collected over the last ten years have demonstrated that f-channels are also present in non-pacemaker cardiomyocytes, and become upregulated in cardiac hypertrophy and failure. Mislocalized expression and/or overexpression of f-channels are a consequence of electrophysiological remodeling and, from a clinical point of view, may represent an arrhythmogenic mechanism in heart failure, a condition associated with a high risk for sudden cardiac death. The potential arrhythmogenic role of I-f and the availability of selective f-channel blockers cause I-f to be a suitable therapeutic target in heart disease. (c) 2006 Elsevier Ltd. All rights reserved.
机构:
Univ Kentucky, Gill Heart Inst, Div Cardiovasc Med, Lexington, KY 40536 USAUniv Kentucky, Gill Heart Inst, Div Cardiovasc Med, Lexington, KY 40536 USA
Post, SR
Hammond, HK
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机构:Univ Kentucky, Gill Heart Inst, Div Cardiovasc Med, Lexington, KY 40536 USA
Hammond, HK
Insel, PA
论文数: 0引用数: 0
h-index: 0
机构:Univ Kentucky, Gill Heart Inst, Div Cardiovasc Med, Lexington, KY 40536 USA
机构:
Univ Kentucky, Gill Heart Inst, Div Cardiovasc Med, Lexington, KY 40536 USAUniv Kentucky, Gill Heart Inst, Div Cardiovasc Med, Lexington, KY 40536 USA
Post, SR
Hammond, HK
论文数: 0引用数: 0
h-index: 0
机构:Univ Kentucky, Gill Heart Inst, Div Cardiovasc Med, Lexington, KY 40536 USA
Hammond, HK
Insel, PA
论文数: 0引用数: 0
h-index: 0
机构:Univ Kentucky, Gill Heart Inst, Div Cardiovasc Med, Lexington, KY 40536 USA