钾通道
耐火期
内科学
有效耐火期
化学
膜片钳
心脏病学
心肌细胞
心房动作电位
心房颤动
电生理学
药理学
医学
内分泌学
复极
作者
Alexander Burashnikov,Héctor Barajas-Martínez,Dan Hu,Victoria M. Robinson,Morten Grunnet,Charles Antzelevitch
出处
期刊:Journal of Cardiovascular Pharmacology
[Ovid Technologies (Wolters Kluwer)]
日期:2020-05-20
卷期号:76 (2): 164-172
被引量:9
标识
DOI:10.1097/fjc.0000000000000855
摘要
Abstract: The mechanisms underlying atrial-selective prolongation of effective refractory period (ERP) and suppression of atrial fibrillation (AF) by NS8593 and UCL1684, small conductance calcium-activated potassium (SK) channel blockers, are poorly defined. The purpose of the study was to confirm the effectiveness of these agents to suppress AF and to probe the underlying mechanisms. Transmembrane action potentials and pseudoelectrocardiograms were recorded from canine isolated coronary-perfused canine atrial and ventricular wedge preparations. Patch clamp techniques were used to record sodium channel current (I Na ) in atrial and ventricular myocytes and human embryonic kidney cells. In both atria and ventricles, NS8593 (3–10 µM) and UCL1684 (0.5 µM) did not significantly alter action potential duration, suggesting little to no SK channel inhibition. Both agents caused atrial-selective: (1) prolongation of ERP secondary to development of postrepolarization refractoriness, (2) reduction of V max , and (3) increase of diastolic threshold of excitation (all are sodium-mediated parameters). NS8593 and UCL1684 significantly reduced I Na density in human embryonic kidney cells as well as in atrial but not in ventricular myocytes at physiologically relevant holding potentials. NS8593 caused a shift of steady-state inactivation to negative potentials in atrial but not ventricular cells. NS8593 and UCL1684 prevented induction of acetylcholine-mediated AF in 6/6 and 8/8 preparations, respectively. This anti-AF effect was associated with strong rate-dependent depression of excitability. The SK channel blockers, NS8593 and UCL1684, are effective in preventing the development of AF due to potent atrial-selective inhibition of I Na , causing atrial-selective prolongation of ERP secondary to induction of postrepolarization refractoriness.
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