Hostetler K Y, Reasor M J, Walker E R, Yazaki P J, Frazee B W
Biochim Biophys Acta. 1986 Feb 12;875(2):400-5. doi: 10.1016/0005-2760(86)90192-x.
Amiodarone is effective in the treatment of ventricular and supraventricular arrhythmias. In man its clinical use is associated with the accumulation of phospholipid-rich multilamellar inclusions in various tissues including lung, liver and others. This report presents evidence showing that amiodarone is a potent inhibitor of lysosomal phospholipase A from rat alveolar macrophages, J-744 macrophages and rat liver. When compared with other cationic amphiphilic agents which are known to produce phospholipidosis, amiodarone is one of the most potent inhibitors yet discovered. The subcellular localization of amiodarone has been determined in lung and its distribution was consistent with a lysosomal localization. It is hypothesized that amiodarone causes cellular phospholipidosis by concentrating in lysosomes and inhibiting phospholipid catabolism.
胺碘酮对室性和室上性心律失常的治疗有效。在人体中,其临床应用与包括肺、肝等在内的各种组织中富含磷脂的多层包涵体的积累有关。本报告提供的证据表明,胺碘酮是大鼠肺泡巨噬细胞、J - 744巨噬细胞和大鼠肝脏溶酶体磷脂酶A的有效抑制剂。与已知会导致磷脂沉积症的其他阳离子两亲性药物相比,胺碘酮是迄今发现的最有效的抑制剂之一。已确定胺碘酮在肺中的亚细胞定位,其分布与溶酶体定位一致。据推测,胺碘酮通过集中在溶酶体中并抑制磷脂分解代谢而导致细胞磷脂沉积症。