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Transient outward K+ current (ITO) reduction prolongs action potentials and promotes afterdepolarisations : a dynamic-clamp study in human and rabbit cardiac atrial myocytes

机译:瞬时向外K +电流(ITO)降低可延长动作电位并促进去极化作用:一项对人和兔心脏心房肌细胞的动态钳位研究

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摘要

Background & aim. Human atrial transient outward K+ current (ITO) is decreased in a variety of cardiac pathologies, but how ITO reduction alters action potentials (AP) and arrhythmia mechanisms is poorly understood, owing to non-selectivity of ITO blockers. Aim: to investigate effects of selective ITO changes on AP shape and duration (APD), and on afterdepolarisations or abnormal automaticity with beta-adrenergic-stimulation, using the dynamic-clamp technique in atrial cells. Methods & Results. Human and rabbit atrial cells were isolated by enzymatic dissociation, and electrical activity recorded by whole-cell-patch clamp (35-37oC). Dynamic-clamp-simulated ITO reduction or block slowed AP phase 1 and elevated the plateau, significantly prolonging APD, in both species. In human atrial cells, ITO block (100% ITO subtraction) increased APD50 by 31%, APD90 by 17%, and APD-61mV (reflecting cellular effective refractory period) by 22% (P
机译:背景与目标。在各种心脏病中,人心房瞬时向外K +电流(ITO)都会降低,但是由于ITO阻滞剂的非选择性,人们对ITO降低如何改变动作电位(AP)和心律不齐的机制了解甚少。目的:使用动态钳技术研究心房细胞中选择性ITO改变对AP形状和持续时间(APD)以及β-肾上腺素能刺激对去极化或异常自动性的影响。方法与结果。通过酶促离解分离人和兔子的心房细胞,并用全细胞膜片钳(35-37oC)记录电活动。动态钳夹模拟的ITO减少或阻止慢速AP阶段1和升高平台期,显着延长两种物种的APD。在人心房细胞中,ITO阻滞(100%ITO减法)使APD50增加31%,使APD90增加17%,使APD-61mV(反映细胞有效不应期)增加22%(P

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