Abramovich-Sivan S, Akselrod S
Abramson Institute of Medical Physics, Sackler Faculty of Exact Sciences, Tel Aviv University, Israel.
J Theor Biol. 1998 May 21;192(2):219-34. doi: 10.1006/jtbi.1998.0658.
In this study we present a computer model of a pacemaker cell subjected to vagal stimulation. This model allows us to investigate the entrainment phenomena of the pacemaker cell resulting from its dynamic interaction with a periodic train of vagal bursts. The possibility of entrainment depends mainly on the fact that a vagal stimulation discharge can "correct" the pacemaker rhythm by an amount that depends on its instantaneous relationship to the pacemaker cycle length. This very simple model, is based on the two most important functional properties of the cardiac pacemaker cells. The first property is the intrinsic pacemaker cycle length, which is an "internal" parameter of the cell, describing the most basic feature of a pacemaker cell. The second one is the phase response curve (PRC), which is an "overall collective" function, containing all the "information" about the possible interactions between the pacemaker cell and the outside world (i.e. its interaction with surrounding cells, external stimulus, etc.). A "collective" PRC was reconstructed from the resulting effects of all the pulses composing a burst. It appears that the PRC parameters as well as the vagal burst parameters are important factors in predicting the entrainment phenomena. Specifically, we found that the tendency of the pacemaker cell to become synchronized with bursts of vagal activity is greater, the larger the number of pulses per burst. However, increasing the number of pulses may also increase the tendency of the pacemaker towards instability, which was unveiled as changes in the configuration of the "collective" PRC. We applied the periodic train of vagal bursts so as to simulate the respiratory sinus arrhythmia (RSA) modulation on the pacemaker cell. We included also a modulation of sympathetic origin, represented as periodic changes in the intrinsic pacemaker cycle length. The frequency response of the pacemaker to "autonomic" modulations allowed us to demonstrate that the RSA dynamics can be interpreted in terms of the entrainment of the pacemaker cell by the respiratory modulation of vagal activity.
在本研究中,我们展示了一个受迷走神经刺激的起搏器细胞的计算机模型。该模型使我们能够研究起搏器细胞与周期性迷走神经冲动序列动态相互作用所产生的同步现象。同步的可能性主要取决于这样一个事实,即迷走神经刺激放电能够以取决于其与起搏器周期长度的瞬时关系的量来“校正”起搏器节律。这个非常简单的模型基于心脏起搏器细胞的两个最重要的功能特性。第一个特性是固有起搏器周期长度,它是细胞的一个“内部”参数,描述了起搏器细胞的最基本特征。第二个特性是相位响应曲线(PRC),它是一个“整体集合”函数,包含了关于起搏器细胞与外界(即其与周围细胞、外部刺激等的相互作用)之间可能相互作用的所有“信息”。从构成一个脉冲串的所有脉冲的结果效应中重建了一个“集合”PRC。看来PRC参数以及迷走神经脉冲串参数是预测同步现象的重要因素。具体而言,我们发现,每个脉冲串中的脉冲数量越多,起搏器细胞与迷走神经活动脉冲串同步的趋势就越大。然而,增加脉冲数量也可能增加起搏器不稳定的趋势,这表现为“集合”PRC构型的变化。我们应用周期性的迷走神经脉冲串来模拟起搏器细胞上的呼吸性窦性心律不齐(RSA)调制。我们还纳入了交感神经起源的调制,表现为固有起搏器周期长度的周期性变化。起搏器对“自主神经”调制的频率响应使我们能够证明,RSA动态可以用起搏器细胞被迷走神经活动的呼吸调制同步来解释。