In vitro electrophysiological mechanisms for antiarrhythmic efficacy of resveratrol, a red wine antioxidant

被引:45
作者
Chen, Wen-Pin
Su, Ming-Jai
Hung, Li-Man
机构
[1] Chang Gung Univ, Coll Med, Dept Life Sci, Tao Yuan 333, Taiwan
[2] Natl Taiwan Univ, Coll Med, Inst Pharmacol, Taipei 10764, Taiwan
关键词
cardiac arrhythmia; electrophysiology; ischemia/reperfusion; resveratrol;
D O I
10.1016/j.ejphar.2006.10.016
中图分类号
R9 [药学];
学科分类号
1007 [药学];
摘要
Resveratrol (trans-3,4',5-trihydroxystilbene),a natural antioxidant derived from grapes, has beneficial effects against coronary heart disease. Its electrophysiological characteristics for antiarrhythmic efficacy are largely unknown; thus, this study aims to explore the resveratrol's antiarrhythmic effects and conduction system in isolated hearts as well as its electrophysiological effects on cardiac myocytes. In the experiment, resveratrol suppressed the ischemia/reperfusion-induced ventricular arrhythmias in Langendorff-perfused rat hearts. In the current clamp study of the experiment, resveratrol prolonged the action potential duration (APD(50) and APD(90)) and suppressed the upstroke velocity of the action potential (V-max) In the voltage clamp study, resveratrol inhibited sodium inward current (I-Na) in a concentration-dependent manner and negative-shifted the voltage-dependent inactivation curve. Resveratrol also reduced the calcium inward current (I-Ca, 51.2 +/- 13.3% at 100 mu M). Furthermore, the transient (I-to) and sustained (I-ss) outward potassium currents were decreased 60.2 +/- 5.7% and 42.3 +/- 5.2% after exposure to resveratrol (100 mu M), respectively. The inward rectifier potassium current (I-K1) was also reduced 24.2 +/- 7.0% in the presence of resveratrol (100 mu M). In the isolated heart perfusion model, resveratrol (100 mu M) prolonged AV nodal refractory period, the Wenckebach cycle length and the conduction through AV node and His-Purkinje system. In conclusion, resveratrol increased the cardiac effective refractory period mainly through inhibiting the ionic channels including I-Na, I-to and I-ss which could contribute to the conversion of ischemia/reperfusion-induced lethal arrhythmias. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:196 / 204
页数:9
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