Himel Herman D, Cupelli Michael, Gantt Martin, Boutjdir Mohamed, El-Sherif Nabil
VA New York Harbor VA Healthcare System, Brooklyn, NY.
Downstate Medical Center, State University of New York, Brooklyn, NY.
Ann Noninvasive Electrocardiol. 2019 Jul;24(4):e12647. doi: 10.1111/anec.12647. Epub 2019 Mar 21.
Successful initiation of spiral wave reentry in the neonatal rat ventricular myocyte (NRVM) monolayer implicitly assumes the presence of spatial dispersion of repolarization (DR), which is difficult to quantify. We recently introduced a NRVM monolayer that utilizes anthopleurin-A to impart a prolonged plateau to the NRVM action potential. This was associated with a significant degree of spatial DR that lends itself to accurate quantification.
We utilized the monolayer and fluorescence optical mapping of intracellular calcium transients (F ) to systematically study and compare the contribution of spatial dispersion of the duration of F (as a surrogate of DR) to induction of spiral wave reentry around a functional core versus reentry around a fixed anatomical obstacle. We show that functional reentry could be initiated by a premature stimulus acting on a substrate of spatial DR resulting in a functional line of propagation block. Subsequent wave fronts circulated around a central core of functional obstacle created by sustained depolarization from the circulating wave front. Both initiation and termination of spiral wave reentry around an anatomical obstacle consistently required participation of a region of functional propagation block. This region was similarly based on spatial DR. Spontaneous termination of spiral wave reentry also resulted from block in the functional component of the circuit obstacle, usually preceded by beat-to-beat slowing of propagation.
The study demonstrates the critical contribution of DR to spiral wave reentry around a purely functional core as well as reentry around a fixed anatomical core.
在新生大鼠心室肌细胞(NRVM)单层中成功引发螺旋波折返隐含地假定了复极化空间离散(DR)的存在,而这很难进行量化。我们最近引入了一种NRVM单层,其利用海葵毒素A使NRVM动作电位的平台期延长。这与显著程度的空间DR相关,这便于进行精确量化。
我们利用该单层以及细胞内钙瞬变(F)的荧光光学映射,系统地研究并比较了F持续时间的空间离散(作为DR的替代指标)对围绕功能性核心的螺旋波折返诱导与围绕固定解剖学障碍物的折返诱导的贡献。我们表明,功能性折返可由作用于空间DR底物的过早刺激引发,导致功能性传播阻滞线。随后的波前围绕由循环波前的持续去极化产生的功能性障碍物中心核心循环。围绕解剖学障碍物的螺旋波折返的起始和终止始终需要功能性传播阻滞区域的参与。该区域同样基于空间DR。螺旋波折返的自发终止也源于电路障碍物功能成分的阻滞,通常之前会有逐搏传播减慢。
该研究证明了DR对围绕纯功能性核心的螺旋波折返以及围绕固定解剖学核心的折返的关键贡献。