Rials S J, Tse W W
J Electrocardiol. 1982;15(3):277-84. doi: 10.1016/s0022-0736(82)80030-7.
The present study examines the hypothesis that vagal activity can accelerate the onset of cardiac arrest produced by administering a beta-adrenergic blocking dose of propranolol to digitoxin-intoxicated dogs. In 11 experiments, intravenous injection of 0.75 mg/kg propranolol into digitoxin intoxicated dogs induced a sustained ventricular asystole (early-phase cardiac arrest). In six of these eleven experiments, intermittent pacing of the ventricles for as long as 150 min to maintain blood pressure after the onset of asystole, led to the resumption of spontaneous heart beats in only one dog. In five other experiments, injection of atropine (1 mg/kg) three min after the onset of early-phase cardiac arrest elicited sustained spontaneous junctional rhythms. In another four experiments the injection of atropine prior to or simultaneously with propranolol prevented the occurrence of asystole and caused the emergence of a junctional pacemaker. In eight experiments in which the cardiac arrest was reversed or prevented, injection of maintenance doses of atropine and propranolol caused eventual failure of the junctional pacemaker (late-phase cardiac arrest). This failure could not be prevented or reversed by atropine. The results suggest that early-phase cardiac arrest is due to vagal suppression of cardiac pacemakers and therefore supports the above hypothesis.
迷走神经活动可加速对洋地黄毒苷中毒的犬给予β-肾上腺素能阻滞剂普萘洛尔剂量后所导致的心脏骤停的发生。在11项实验中,向洋地黄毒苷中毒的犬静脉注射0.75mg/kg普萘洛尔会诱发持续性心室停搏(早期心脏骤停)。在这11项实验中的6项里,在停搏发生后间歇性起搏心室长达150分钟以维持血压,结果仅1只犬恢复了自主心跳。在另外5项实验中,在早期心脏骤停发生3分钟后注射阿托品(1mg/kg)引发了持续性的自主交界性心律。在另外4项实验中,在普萘洛尔之前或同时注射阿托品可防止停搏的发生并导致交界性起搏器的出现。在8项心脏骤停得到逆转或预防的实验中,注射维持剂量的阿托品和普萘洛尔最终导致交界性起搏器功能衰竭(晚期心脏骤停)。阿托品无法预防或逆转这种衰竭。结果表明,早期心脏骤停是由于迷走神经对心脏起搏器的抑制作用,因此支持上述假设。