School of Mathematical Sciences, Rochester Institute of Technology, 85 Lomb Memorial Drive, Rochester, NY 14623, USA.
J Theor Biol. 2011 Sep 21;285(1):164-76. doi: 10.1016/j.jtbi.2011.06.039. Epub 2011 Jul 8.
Increased dispersion of action potential duration across cardiac tissue has long been considered an important substrate for the development of most electrical arrhythmias. Although this dispersion has been studied previously by characterizing the static intrinsic gradients in cellular electrophysiology and dynamical gradients generated by fast pacing, few studies have concentrated on dispersions generated solely by structural effects. Here we show how boundaries and geometry can produce spatially dependent changes in action potential duration (APD) in homogeneous and isotropic tissue, where all the cells have the same APD in the absence of diffusion. Electrotonic currents due to coupling within the tissue and at the tissue boundaries can generate dispersion, and the profile of this dispersion can change dramatically depending on tissue size and shape, action potential morphology, tissue dimensionality, and stimulus frequency and location. The dispersion generated by pure geometrical effects can be on the order of tens of milliseconds, enough under certain conditions to produce conduction blocks and initiate reentrant waves.
动作电位时程在心脏组织中的离散度增加一直被认为是大多数电心律失常发展的重要基质。尽管先前已经通过描述细胞电生理学中的静态固有梯度和快速起搏产生的动态梯度来研究这种离散度,但很少有研究集中在仅由结构效应产生的离散度上。在这里,我们展示了边界和几何形状如何在均匀各向同性组织中产生动作电位时程(APD)的空间依赖性变化,在不存在扩散的情况下,所有细胞在没有扩散的情况下具有相同的 APD。组织内和组织边界处的电耦合电流会产生离散度,并且这种离散度的分布可以根据组织大小和形状、动作电位形态、组织维度以及刺激频率和位置而发生剧烈变化。仅由纯几何效应产生的离散度可能为数毫秒,在某些条件下足以产生传导阻滞并引发折返波。