Key Laboratory of Medical Electrophysiology of Ministry of Education, Medical Electrophysiology Key Lab of Sichuan Province, Institute of Cardiovascular Research, Southwest Medical University, Luzhou, Sichuan, China (mainland).
Department of Electrocardiography, The Affiliated Traditional Chinese Medicine Hospital of Southwest Medical University, Luzhou, Sichuan, China (mainland).
Med Sci Monit. 2020 May 29;26:e924215. doi: 10.12659/MSM.924215.
BACKGROUND Dysfunction of small conductance calcium activated potassium (SK) channels plays a vital role in atrial arrhythmogenesis. Amiodarone and dronedarone are the most effective class III antiarrhythmic drugs. It is unclear whether the antiarrhythmic effect of amiodarone and dronedarone is related to SK channel inhibition. MATERIAL AND METHODS Tissue samples were obtained from the right atria of 46 patients with normal sinus rhythm and 39 patients with chronic atrial fibrillation. Isolated atrial myocytes were obtained by enzymatic dissociation. KCNN2 (SK2) channels were transiently expressed in human embryonic kidney (HEK)-293 cells. SK currents were recorded using whole-cell conventional patch clamp techniques. RESULTS Amiodarone and dronedarone showed a concentration-dependent inhibitory effect on SK currents (IKAS) in atrial myocytes from normal sinus rhythm patients and chronic atrial fibrillation patients. The suppressed efficacy of dronedarone and amiodarone on IKAS was greater in atrial myocytes from chronic atrial fibrillation patients than that from normal sinus rhythm patients. Furthermore, in patients with chronic atrial fibrillation, the IC₅₀ value was 2.42 µM with dronedarone and 8.03 µM with amiodarone. In HEK-293 cells with transiently transfected SK2 channels, both dronedarone and amiodarone had a dose-dependent inhibitory effect on IKAS. The IC₅₀ value was 1.7 µM with dronedarone and 7.2 µM with amiodarone in cells from patients with chronic atrial fibrillation. Compared to amiodarone, dronedarone is more efficacy to inhibit IKAS and could be a potential intervention for patients with chronic atrial fibrillation. CONCLUSIONS Dronedarone provides a great degree of IKAS inhibition in atrial myocytes from chronic atrial fibrillation than amiodarone. IKAS might be a potential target of amiodarone and dronedarone for the management of chronic atrial fibrillation.
小电导钙激活钾(SK)通道功能障碍在心房心律失常发生中起着至关重要的作用。胺碘酮和决奈达隆是最有效的 III 类抗心律失常药物。胺碘酮和决奈达隆的抗心律失常作用是否与 SK 通道抑制有关尚不清楚。
组织样本取自 46 例窦性节律正常患者和 39 例慢性心房颤动患者的右心房。通过酶解分离获得分离的心房肌细胞。KCNN2(SK2)通道在人胚肾(HEK)-293 细胞中瞬时表达。使用全细胞膜片钳技术记录 SK 电流。
胺碘酮和决奈达隆对窦性节律正常患者和慢性心房颤动患者的心房肌细胞 SK 电流(IKAS)呈浓度依赖性抑制作用。与窦性节律正常患者的心房肌细胞相比,慢性心房颤动患者的心房肌细胞中,决奈达隆和胺碘酮对 IKAS 的抑制作用更强。此外,在慢性心房颤动患者中,IC₅₀ 值为 2.42µM 时为决奈达隆,8.03µM 时为胺碘酮。在瞬时转染 SK2 通道的 HEK-293 细胞中,决奈达隆和胺碘酮对 IKAS 均具有剂量依赖性抑制作用。在慢性心房颤动患者的细胞中,IC₅₀ 值为 1.7µM 时为决奈达隆,7.2µM 时为胺碘酮。与胺碘酮相比,决奈达隆对 IKAS 的抑制作用更大,可能是慢性心房颤动患者的潜在干预措施。
与胺碘酮相比,决奈达隆在慢性心房颤动的心房肌细胞中提供了更大程度的 IKAS 抑制。IKAS 可能是胺碘酮和决奈达隆治疗慢性心房颤动的潜在靶点。