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地尔硫䓬和硝苯地平对人心房肌细胞瞬时外向钾电流和超快速延迟整流钾电流的影响。

Effects of diltiazem and nifedipine on transient outward and ultra-rapid delayed rectifier potassium currents in human atrial myocytes.

作者信息

Gao Zhan, Sun Haiying, Chiu Shui-Wah, Lau Chu-Pak, Li Gui-Rong

机构信息

Department of Medicine and Research Centre of Heart, Brain, Hormone and Health Aging, The University of Hong Kong, Pokfulam, Hong Kong SAR, China.

出版信息

Br J Pharmacol. 2005 Feb;144(4):595-604. doi: 10.1038/sj.bjp.0706113.

Abstract
  1. It is unknown whether the widely used L-type Ca(2+) channel antagonists diltiazem and nifedipine would block the repolarization K(+) currents, transient outward current (I(to1)) and ultra-rapid delayed rectifier K(+) current (I(Kur)), in human atrium. The present study was to determine the effects of diltiazem and nifedipine on I(to1) and I(Kur) in human atrial myocytes with whole-cell patch-clamp technique. 2. It was found that diltiazem substantially inhibited I(to1) in a concentration-dependent manner, with an IC(50) of 29.2+/-2.4 microM, and nifedipine showed a similar effect (IC(50)=26.8+/-2.1 muM). The two drugs had no effect on voltage-dependent kinetics of the current; however, they accelerated I(to1) inactivation significantly, suggesting an open channel block. 3. In addition, diltiazem and nifedipine suppressed I(Kur) in a concentration-dependent manner (at +50 mV, IC(50)=11.2+/-0.9 and 8.2+/-0.8 microM, respectively). These results indicate that the Ca(2+) channel blockers diltiazem and nifedipine substantially inhibit I(to1) and I(Kur) in human atrial myocytes.
摘要
  1. 广泛使用的L型钙通道拮抗剂地尔硫䓬和硝苯地平是否会阻断人心房的复极化钾电流、瞬时外向电流(I(to1))和超快速延迟整流钾电流(I(Kur))尚不清楚。本研究旨在采用全细胞膜片钳技术测定地尔硫䓬和硝苯地平对人心房肌细胞I(to1)和I(Kur)的影响。2. 发现地尔硫䓬以浓度依赖性方式显著抑制I(to1),半数抑制浓度(IC(50))为29.2±2.4微摩尔,硝苯地平表现出类似作用(IC(50)=26.8±2.1微摩尔)。这两种药物对电流的电压依赖性动力学无影响;然而,它们显著加速I(to1)失活,提示为开放通道阻滞。3. 此外,地尔硫䓬和硝苯地平以浓度依赖性方式抑制I(Kur)(在+50毫伏时,IC(50)分别为11.2±0.9和8.2±0.8微摩尔)。这些结果表明,钙通道阻滞剂地尔硫䓬和硝苯地平可显著抑制人心房肌细胞的I(to1)和I(Kur)。

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