Golovina V A, Zakharov S I, Rosenshtraukh L V
Department of Heart Electrophysiology, USSR Cardiology Research Center, Moscow.
J Mol Cell Cardiol. 1988 Apr;20(4):303-11. doi: 10.1016/s0022-2828(88)80064-6.
The effects of ryanodine on (1) ventricular arrhythmias in guinea-pigs in vivo, (2) delayed afterpotentials and aftercontractions and (3) spontaneous oscillations of the membrane potential (SOP) and of resting tension (SOT) of guinea-pig papillary muscle under ouabain intoxication have been studied. After addition of ouabain (1 microM), the afterpotentials, aftercontractions and the amplitude of SOP and SOT were significantly increased. The power spectra of SOT and SOP under these conditions had a resonance harmonic with a frequency of about 5 Hz. The afterpotentials, aftercontractions, SOP and SOT were abolished 3 to 5 min after ryanodine addition (0.1 to 0.5 microM), suggesting a close relationship between these oscillations and the oscillatory activity of sarcoplasmic reticulum. During in vivo experiments, ouabain-induced (75 to 115 micrograms/kg) ventricular arrhythmias were terminated 4 to 5 min after the intravenous injection of ryanodine (15 micrograms/kg) and within 8 to 10 min, the sinus rhythm was completely restored. We conclude that the antiarrhythmic effect of ryanodine is related to the inhibition of the diastolic fluctuations of the membrane potential.
研究了ryanodine对以下方面的影响:(1)豚鼠体内的室性心律失常;(2)延迟后电位和后收缩;(3)哇巴因中毒状态下豚鼠乳头肌的膜电位自发振荡(SOP)和静息张力自发振荡(SOT)。加入哇巴因(1 microM)后,后电位、后收缩以及SOP和SOT的幅度显著增加。在这些条件下,SOT和SOP的功率谱具有频率约为5 Hz的共振谐波。加入ryanodine(0.1至0.5 microM)后3至5分钟,后电位、后收缩、SOP和SOT消失,提示这些振荡与肌浆网的振荡活动密切相关。在体内实验中,静脉注射ryanodine(15 micrograms/kg)后4至5分钟,哇巴因诱导的(75至115 micrograms/kg)室性心律失常终止,8至10分钟内窦性心律完全恢复。我们得出结论,ryanodine的抗心律失常作用与抑制膜电位的舒张期波动有关。