Jalife J, Slenter V A, Salata J J, Michaels D C
Circ Res. 1983 Jun;52(6):642-56. doi: 10.1161/01.res.52.6.642.
Dynamic heart rate control by parasympathetic nervous input involves feedback mechanisms and reflex bursting of efferent cardiac vagal fibers. Periodic vagal bursting induces phasic changes in sinoatrial cycle length and can entrain the pacemaker to beat at periods that may be identical to those of the vagal burst. We investigated the electrophysiological basis of these phenomena in isolated sinus node preparations (rabbit, cat, and sheep). In the presence of propranolol (3.9 X 10(-6)M), relatively brief (50-150 msec) trains of stimuli, applied onto the endocardial surface of the preparation, activated postganglionic vagal terminals and induced a brief hyperpolarization of sinoatrial pacemaker cells. This vagally mediated hyperpolarization could alter the pacemaker rhythm by an amount that depended on its duration and its position in the cycle, as well as on the duration of the free-running pacemaker period. When the free-running period was sufficiently long and the hyperpolarization was induced sufficiently early in the spontaneous cycle, a "paradoxical" acceleration of the pacemaker rhythm ensued. Phasic changes were plotted on phase-response curves, constructed by scanning systematically the sinoatrial pacemaker period with single or repetitive vagal trains. These phase-response curves enabled us to predict the entrainment characteristics and the levels of synchronization of the pacemaker to the vagal periodicity. The overall data explain the cellular mechanisms involved in the phasic effects of brief vagal discharges on sinoatrial periodicity, and provide conclusive evidence for the prediction that repetitive vagal input is capable of forcing the cardiac pacemaker to beat at rates that can be faster or slower than the intrinsic pacemaker rate. These data should improve our knowledge of the dynamic control of heart rate by neural reflexes and aid in our understanding of rhythm disturbances generated by the interaction of the cardiac pacemaker with vagal activity.
副交感神经输入对心率的动态控制涉及反馈机制以及传出心脏迷走神经纤维的反射性爆发活动。周期性迷走神经爆发活动会引起窦房结周期长度的阶段性变化,并可使起搏器以与迷走神经爆发活动相同的周期跳动。我们在离体窦房结标本(兔、猫和羊)中研究了这些现象的电生理基础。在普萘洛尔(3.9×10⁻⁶M)存在的情况下,施加于标本心内膜表面的相对短暂(50 - 150毫秒)的刺激序列激活了节后迷走神经末梢,并引起窦房结起搏细胞短暂的超极化。这种由迷走神经介导的超极化可改变起搏节律,其改变程度取决于超极化的持续时间、在周期中的位置以及自主起搏周期的持续时间。当自主起搏周期足够长且在自发周期中足够早地诱导超极化时,会出现起搏器节律的“反常”加速。通过用单个或重复的迷走神经刺激序列系统扫描窦房结起搏周期,绘制出相位响应曲线来呈现阶段性变化。这些相位响应曲线使我们能够预测起搏器与迷走神经周期性的同步特征和同步水平。总体数据解释了短暂迷走神经放电对窦房结周期性产生阶段性影响所涉及的细胞机制,并为重复迷走神经输入能够迫使心脏起搏器以快于或慢于固有起搏速率的频率跳动这一预测提供了确凿证据。这些数据应能增进我们对神经反射对心率动态控制的了解,并有助于我们理解心脏起搏器与迷走神经活动相互作用所产生的节律紊乱。