首页> 外文期刊>Journal of Molecular and Cellular Cardiology >Propafenone inhibition of human atrial myocyte repolarizing currents.
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Propafenone inhibition of human atrial myocyte repolarizing currents.

机译:普罗帕酮抑制人心房肌细胞的复极电流。

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摘要

This study was aimed at defining cellular electropharmacologic effects of propafenone on repolarizing currents in human atrial myocytes. Whole-cell patch-clamp of enzymatically isolated atrial myocytes from 11 cardiac surgical patients aged between 29 days and 74 years revealed potent time- and concentration-dependent (IC50 = 4.8 +/- 0.4 mumol/l), but age-, voltage-, and frequency-independent propafenone inhibition of transient outward current. Time course of apparent transient outward current inactivation was best described by a single exponential process in the absence of propafenone and by a double exponential model in its presence, with drug-concentration-dependent acceleration of the fast exponential component. Neither voltage dependence of steady-state transient outward current inactivation nor time course of recovery from inactivation was affected by propafenone. Significant inhibition (P < 0.05) of the ultra-rapidly activating delayed rectifier and inwardly rectifying currents was observed only in the presence of > or = 10 mumol/l propafenone. These actions of propafenone could explain its repolarization prolonging effect and might contribute to clinical electrophysiologic responses which have been documented in patients of all ages.
机译:这项研究旨在确定普罗帕酮对人心房肌细胞中复极电流的细胞电药理作用。来自11名年龄在29天至74岁之间的心脏外科手术患者的酶促分离心房肌细胞的全细胞膜片钳显示强效的时间和浓度依赖性(IC50 = 4.8 +/- 0.4μmol/ l),但年龄,电压,和频率独立的普罗帕酮抑制瞬态向外电流。表观瞬时外向电流失活的时间过程最好通过在没有普罗帕酮的情况下的单指数过程和在存在普罗帕酮的情况下的双指数模型来描述,其中快速指数成分的浓度依赖于药物的加速。普罗帕酮既不影响稳态瞬态外向电流失活的电压依赖性,也没有影响从失活恢复的时间过程。仅在≥10μmol/ l普罗帕酮的存在下,才观察到对超快活化延迟整流器和向内整流电流的显着抑制(P <0.05)。普罗帕酮的这些作用可以解释其复极化延长作用,并且可能有助于临床电生理反应,这在所有年龄段的患者中都有记载。

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