Efimov I R, Ermentrout B, Huang D T, Salama G
Department of Cell Biology and Physiology, University of Pittsburgh, Pennsylvania, USA.
J Cardiovasc Electrophysiol. 1996 Jun;7(6):512-30. doi: 10.1111/j.1540-8167.1996.tb00558.x.
Substantial progress has been made in our understanding of transmural activation across ventricular muscle through studies of excitation patterns and potential distributions. In contrast, repolarization sequences are poorly understood because of experimental difficulties in mapping action potential durations (APDs) using extracellular electrodes.
Langendorff-perfused guinea pig hearts and isolated coronary-perfused left ventricular sheet preparations were stained with the voltage-sensitive dye RH-421 and optical APs were recorded with a photodiode array. Epicardial maps were constructed using a triangulation method applied to matrices of activation and repolarization times determined from (dF/dt)max and (d2F/dt2)max' respectively. Numerical simulations were carried out based on: (1) a modified Luo-Rudy model; (2) the three-dimensional architecture of ventricular fibers; and (3) the intrinsic spatial distribution of APDs. In ventricular sheets, epicardial stimulation elicited elliptical activation patterns with the major axis aligned with the longitudinal axis of epicardial fibers. When the pacing electrode was progressively inserted from epicardium to endocardium, the major axes rotated gradually, clockwise by 45 degrees, and the eccentricity decreased from 2 to 1.14. Repolarization showed a relatively uniform pattern, independent of pacing site, beginning at the apex and spreading to the base.
In experiments and simulations, the helical rotation of epicardial excitation isochrones caused by pacing at increasing depth in the myocardium correlated with the helical three-dimensional architecture of ventricular fibers. In contrast, repolarization was independent of the activation sequence and was mainly guided by spatial differences in APDs between apex and base.
通过对兴奋模式和电位分布的研究,我们对跨心室肌的透壁激活有了实质性进展。相比之下,由于使用细胞外电极绘制动作电位时程(APD)存在实验困难,复极化序列的了解较少。
用电压敏感染料RH - 421对Langendorff灌注的豚鼠心脏和离体冠状动脉灌注的左心室薄片标本进行染色,并用光电二极管阵列记录光学动作电位。使用三角测量法构建心外膜图,该方法分别应用于由(dF/dt)max和(d2F/dt2)max确定的激活和复极化时间矩阵。基于以下因素进行了数值模拟:(1)改良的Luo - Rudy模型;(2)心室纤维的三维结构;(3)APD的固有空间分布。在心室薄片中,心外膜刺激引发椭圆形激活模式,其长轴与心外膜纤维的纵轴对齐。当起搏电极从心外膜逐渐插入心内膜时,长轴逐渐顺时针旋转45度,偏心率从2降至1.14。复极化呈现相对均匀的模式,与起搏部位无关,从心尖开始并向心底扩散。
在实验和模拟中,心肌中起搏深度增加导致的心外膜兴奋等时线的螺旋旋转与心室纤维的螺旋三维结构相关。相比之下,复极化与激活序列无关,主要由心尖和心底之间APD的空间差异引导。