Wang D W, Kiyosue T, Sato T, Arita M
Department of Physiology, Oita Medical University, Japan.
J Mol Cell Cardiol. 1996 May;28(5):893-903. doi: 10.1006/jmcc.1996.0084.
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.
使用全细胞电压钳技术,在5微摩尔尼群地平阻断L型钙电流的情况下,研究了I类抗心律失常药物西苯唑啉、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。如Sanguinetti和Jurkiewicz(1990年)所报道,IK由两种不同的电流系统组成,即具有强内向整流特性的E4031敏感快速激活成分(IKr)和几乎没有整流的E4031不敏感缓慢激活成分(IKs)。西苯唑啉(30微摩尔)降低了IKr和IKs,而氟卡尼(10和30微摩尔)仅降低了IKr。相比之下,美西律(30微摩尔)对IKr和IKs均无影响。由于抑制IKr和/或IKs会延长动作电位持续时间和不应期,同时具有III类效应的I类药物在治疗某些折返性心律失常时可能具有额外的作用。