Spach Madison S, Heidlage J Francis, Barr Roger C, Dolber Paul C
Department of Pediatrics, Duke University Medical Center, Durham, NC 27710, USA.
Heart Rhythm. 2004 Oct;1(4):500-15. doi: 10.1016/j.hrthm.2004.06.010.
With the advent of new information about alterations of cardiac gap junctions in disease conditions associated with arrhythmias, there have been major advances in the genetic and metabolic manipulation of gap junctions. In contrast, in naturally occurring cardiac preparations, little is known about cell-to-cell transmission and the subcellular events of propagation or about structural mechanisms that may affect conduction events at this small size scale. Therefore, the aim of this article is to review results that produce the following unifying picture: changes in cardiac conduction due to remodeling cardiac morphology ultimately are limited to changes in three morphologic parameters: (1) cell geometry (size and shape), (2) gap junctions (distribution and conductivity), and (3) interstitial space (size and distribution). In this article, we consider changes in conduction that result from the remodeling of cell size and gap junction distribution that occurs with developmental ventricular hypertrophy from birth to maturity. We then go on to changes in longitudinal and transverse propagation in aging human atrial bundles that are produced by remodeling interstitial space due to deposition of collagenous septa. At present, experimental limitations in naturally occurring preparations prevent measurement of the conductance of individual gap junctional plaques, as well as the delays in conduction associated with cell-to-cell transmission. Therefore, we consider the development of mathematical electrical models based on documented cardiac microstructure to gain insight into the role of specific morphologic parameters in generating the changes in anisotropic propagation that we measured in the tissue preparations. A major antiarrhythmic implication of the results is that an "indirect" therapeutic target is interstitial collagen, because regulation of its deposition and turnover to prevent or alter microfibrosis can enhance side-to-side electrical coupling between small groups of cells in aging atrial bundles.
随着与心律失常相关疾病状态下心脏缝隙连接改变的新信息出现,缝隙连接的基因和代谢操纵取得了重大进展。相比之下,在天然的心脏制剂中,关于细胞间传递以及传播的亚细胞事件,或者关于在这种小尺寸尺度上可能影响传导事件的结构机制,人们所知甚少。因此,本文的目的是回顾一些结果,这些结果呈现出以下统一的图景:由于心脏形态重塑导致的心脏传导变化最终仅限于三个形态学参数的变化:(1)细胞几何形状(大小和形状),(2)缝隙连接(分布和电导率),以及(3)细胞间质空间(大小和分布)。在本文中,我们考虑从出生到成熟发育性心室肥大过程中发生的细胞大小和缝隙连接分布重塑所导致的传导变化。然后我们继续探讨在衰老的人心房束中,由于胶原隔沉积导致细胞间质空间重塑而产生的纵向和横向传播的变化。目前,天然制剂中的实验局限性使得无法测量单个缝隙连接斑块的电导率,以及与细胞间传递相关的传导延迟。因此,我们考虑基于已记录的心脏微观结构开发数学电模型,以深入了解特定形态学参数在产生我们在组织制剂中测量到的各向异性传播变化中的作用。这些结果的一个主要抗心律失常意义在于,一个“间接”的治疗靶点是细胞间质胶原蛋白,因为调节其沉积和周转以预防或改变微纤维化可以增强衰老心房束中小细胞群之间的侧向电耦合。