首页> 外文期刊>Journal of Molecular and Cellular Cardiology >Comparison of the effects of class I anti-arrhythmic drugs, cibenzoline, mexiletine and flecainide, on the delayed rectifier K+ current of guinea-pig ventricular myocytes.
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Comparison of the effects of class I anti-arrhythmic drugs, cibenzoline, mexiletine and flecainide, on the delayed rectifier K+ current of guinea-pig ventricular myocytes.

机译:比较I类抗心律不齐药物cibenzoline,美西律和氟卡尼对豚鼠心室肌​​细胞延迟整流K +电流的作用。

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摘要

The effect of class I anti-arrhythmic drugs, cibenzoline, mexiletine and flecainide, on the delayed rectifier potassium current (IK) in guinea-pig ventricular myocytes was studied using whole cell voltage clamp techniques and under blockade of the L-type calcium current by 5 microM nitrendipine. IK consisted of two different current systems, as reported by Sanguinetti and Jurkiewicz (1990), i.e. an E4031-sensitive rapidly activating component (IKr) with a strong inward-going rectification property and an E4031-insensitive slowly activating component (IKs) with little rectification. Cibenzoline (30 microM) decreased both IKr and IKs while flecainide (10 and 30 microM) decreased the IKr exclusively. Mexiletine (30 microM), in contrast, affected neither IKr nor IKs. Since the inhibition of IK(r) and/or IKs prolongs duration of action potentials and refractory periods, class I drugs which also possess the class III effect may have additional effects in treating certain re-entrant arrhythmias.
机译:使用全细胞电压钳技术研究了I类抗心律不齐药物cibenzoline,美西律和氟卡尼对豚鼠心室肌​​细胞延迟整流钾电流(IK)的影响,并通过阻断L型钙电流的作用5 microM尼群地平。 IK由Sanguinetti和Jurkiewicz(1990)报道,由两种不同的电流系统组成,即具有强向内整流特性的E4031敏感快速活化组分(IKr)和几乎没有E4031敏感的缓慢活化组分(IKs)整改。 Cibenzoline(30 microM)降低IKr和IKs,而flecainide(10和30 microM)仅降低IKr。相反,美西律(30 microM)既不影响IKr,也不影响IK。由于IK(r)和/或IKs的抑制作用延长了动作电位和不应期的持续时间,因此具有I类III类作用的I类药物在治疗某些折返性心律不齐中可能具有其他作用。

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