Nonchannel drug targets in atrial fibrillation

被引:40
作者
Goette, A
Lendeckel, U
机构
[1] Otto Von Guericke Univ, Div Cardiol, D-39120 Magdeburg, Germany
[2] Otto Von Guericke Univ, Inst Expt Internal Med, D-39120 Magdeburg, Germany
关键词
atrial fibrillation; molecular biology; signal transduction; pharmacology; therapy;
D O I
10.1016/j.pharmthera.2004.01.001
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Atrial fibrillation (AF) is the most common clinical arrhythmia and one of the most important factors for ischemic stroke. In general, AF is treated with "channel-blocking drugs" to restore sinus rhythm and warfarin is recommended in the majority of patients to prevent atrial thrombus formation and thromboembolic events. In the recent years, a tremendous amount has been learned about the pathophysiology and molecular biology of AF Thus, pharmacologic interference with specific signal transduction pathways with "non-channel-blocking drugs" appears promising as a novel antiarrhythmic approach to maintain sinus rhythm and to prevent atrial clot formation. Therefore, this review will highlight some novel "nonchannel drug targets" for AF therapy. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:17 / 36
页数:20
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