Department of Internal Medicine, Center for Arrhythmia Research, University of Michigan, Ann Arbor, MI (R.P.M., K.K., E.H., R.J.R., B.C.W., D.F.-R., S.R.E., Y.T., D.P.-B., M.Z., R.P.O., H.M., G.G.-S., U.M.R.A., S.V.P., O.B., J.J.); Department of Surgery, University of Rochester, Rochester, NY (M.F.S.); and Department of Engineering, Norfolk State University, Norfolk, VA (S.B., M.D.).
Circulation. 2014 Apr 8;129(14):1472-82. doi: 10.1161/CIRCULATIONAHA.113.004742. Epub 2014 Jan 24.
Little is known about the mechanisms underlying the transition from paroxysmal to persistent atrial fibrillation (AF). In an ovine model of long-standing persistent AF we tested the hypothesis that the rate of electric and structural remodeling, assessed by dominant frequency (DF) changes, determines the time at which AF becomes persistent.
Self-sustained AF was induced by atrial tachypacing. Seven sheep were euthanized 11.5±2.3 days after the transition to persistent AF and without reversal to sinus rhythm; 7 sheep were euthanized after 341.3±16.7 days of long-standing persistent AF. Seven sham-operated animals were in sinus rhythm for 1 year. DF was monitored continuously in each group. Real-time polymerase chain reaction, Western blotting, patch clamping, and histological analyses were used to determine the changes in functional ion channel expression and structural remodeling. Atrial dilatation, mitral valve regurgitation, myocyte hypertrophy, and atrial fibrosis occurred progressively and became statistically significant after the transition to persistent AF, with no evidence for left ventricular dysfunction. DF increased progressively during the paroxysmal-to-persistent AF transition and stabilized when AF became persistent. Importantly, the rate of DF increase correlated strongly with the time to persistent AF. Significant action potential duration abbreviation, secondary to functional ion channel protein expression changes (CaV1.2, NaV1.5, and KV4.2 decrease; Kir2.3 increase), was already present at the transition and persisted for 1 year of follow up.
In the sheep model of long-standing persistent AF, the rate of DF increase predicts the time at which AF stabilizes and becomes persistent, reflecting changes in action potential duration and densities of sodium, L-type calcium, and inward rectifier currents.
阵发性到持续性心房颤动(AF)的机制知之甚少。在长期持续性 AF 的羊模型中,我们测试了以下假设,即电重构和结构重构的速率,通过主频(DF)变化来评估,决定 AF 变为持续性的时间。
通过心房快速起搏诱导自持续 AF。7 只羊在持续性 AF 转为持续性 AF 后 11.5±2.3 天且未恢复窦性节律时安乐死;7 只羊在持续性 AF 持续 341.3±16.7 天后安乐死。7 只假手术动物维持窦性心律 1 年。在每个组中持续监测 DF。使用实时聚合酶链反应、Western blot、膜片钳和组织学分析来确定功能离子通道表达和结构重构的变化。心房扩张、二尖瓣反流、心肌细胞肥大和心房纤维化在持续性 AF 转变后逐渐发生并具有统计学意义,没有左心室功能障碍的证据。DF 在阵发性到持续性 AF 转变过程中逐渐增加,当 AF 变得持续时稳定下来。重要的是,DF 增加的速率与持续性 AF 的时间密切相关。由于功能性离子通道蛋白表达变化(CaV1.2、NaV1.5 和 KV4.2 减少;Kir2.3 增加)导致动作电位持续时间缩短,在转变时已经存在,并持续了 1 年的随访。
在长期持续性 AF 的羊模型中,DF 增加的速率预测 AF 稳定并变为持续性的时间,反映了动作电位持续时间和钠、L 型钙和内向整流电流密度的变化。