Department of Medicine, David Geffen School of Medicine, University of California, Los Angeles, California.
Department of Computational Medicine, David Geffen School of Medicine, University of California, Los Angeles, California.
Am J Physiol Heart Circ Physiol. 2021 Feb 1;320(2):H826-H837. doi: 10.1152/ajpheart.00608.2020. Epub 2021 Jan 1.
Spiral wave reentry as a mechanism of lethal ventricular arrhythmias has been widely demonstrated in animal experiments and recordings from human hearts. It has been shown that in structurally normal hearts spiral waves are unstable, breaking up into multiple wavelets via dynamical instabilities. However, many of the second-generation action potential models give rise only to stable spiral waves, raising issues regarding the underlying mechanisms of spiral wave breakup. In this study, we carried out computer simulations of two-dimensional homogeneous tissues using five ventricular action potential models. We show that the transient outward potassium current (), although it is not required, plays a key role in promoting spiral wave breakup in all five models. As the maximum conductance of increases, it first promotes spiral wave breakup and then stabilizes the spiral waves. In the absence of , speeding up the L-type calcium kinetics can prevent spiral wave breakup, however, with the same speedup kinetics, spiral wave breakup can be promoted by increasing . Increasing promotes single-cell dynamical instabilities, including action potential duration alternans and chaos, and increasing further suppresses these action potential dynamics. These cellular properties agree with the observation that increasing first promotes spiral wave breakup and then stabilizes spiral waves in tissue. Implications of our observations to spiral wave dynamics in the real hearts and action potential model improvements are discussed. Spiral wave breakup manifesting as multiple wavelets is a mechanism of ventricular fibrillation. It has been known that spiral wave breakup in cardiac tissue can be caused by a steeply sloped action potential duration restitution curve, a property mainly determined by the recovery of L-type calcium current. Here, we show that the transient outward potassium current () is another current that plays a key role in spiral wave breakup, that is, spiral waves can be stable for low and high maximum conductance but breakup occurs for intermediate maximum conductance. Since is present in normal hearts of many species and required for Brugada syndrome, it may play an important role in the spiral wave stability and arrhythmogenesis under both normal condition and Brugada syndrome.
螺旋波折返作为致命性室性心律失常的机制已在动物实验和人类心脏记录中得到广泛证实。研究表明,在结构正常的心脏中,螺旋波是不稳定的,通过动力学不稳定性会分裂成多个小波。然而,许多第二代动作电位模型仅产生稳定的螺旋波,这引发了关于螺旋波破裂的潜在机制问题。在这项研究中,我们使用五个心室动作电位模型对二维均匀组织进行了计算机模拟。我们表明,虽然暂态外向钾电流()不是必需的,但它在所有五个模型中都对促进螺旋波破裂起着关键作用。随着最大电导的增加,它首先促进螺旋波破裂,然后稳定螺旋波。在不存在的情况下,加快 L 型钙动力学可以防止螺旋波破裂,然而,以相同的速度加快动力学,通过增加可以促进螺旋波破裂。增加会促进单个细胞动力学不稳定性,包括动作电位时程交替和混沌,进一步增加会抑制这些动作电位动力学。这些细胞特性与观察结果一致,即增加首先促进螺旋波破裂,然后稳定组织中的螺旋波。讨论了我们的观察结果对真实心脏中螺旋波动力学和动作电位模型改进的影响。表现为多个小波的螺旋波破裂是室颤的一种机制。众所周知,心脏组织中的螺旋波破裂可能是由动作电位时程恢复曲线斜率陡峭引起的,该特性主要由 L 型钙电流的恢复决定。在这里,我们表明,暂态外向钾电流()是另一种在螺旋波破裂中起关键作用的电流,即螺旋波可以在低和高最大电导下稳定,但在中间最大电导下破裂。由于在许多物种的正常心脏中都存在,并且是 Brugada 综合征所必需的,因此它可能在正常状态和 Brugada 综合征下的螺旋波稳定性和心律失常发生中发挥重要作用。