Chilson R A, Davis L D
J Cardiovasc Pharmacol. 1985 Mar-Apr;7(2):368-76. doi: 10.1097/00005344-198503000-00024.
The effects of hypoxia on the transmembrane potential of dog Purkinje cells in isolated, superfused fiber bundles pretreated with ouabain were studied. Cells stimulated electrically at 93/min were exposed to ouabain, 2.1 X 10(-7) M, until the magnitude of phase 4 depolarization increased to 7-12 mV. Arrhythmias did not occur. Following a 10-min washout period, hypoxic solution (PO2 = 15-50 mm Hg) was applied for 2-5 min. This caused decreases in maximum diastolic potential, overshoot, rising velocity of phase 0, and duration of the action potential. The slope of depolarization during phase 4 increased markedly. Arrhythmias characterized by escape rhythms or single and multiple bursts of premature excitations occurred in greater than 90% of the experiments. None of these changes was noted when identical levels of hypoxia were applied for a similar period to normal cells. Blockade of the beta-adrenergic receptors with propranolol, 0.3 mg/L, did not alter the response of ouabain-pretreated cells to hypoxia in any manner, ruling out release of endogenous catecholamines as essential for the observed effects. These results suggest that ouabain and hypoxia have a synergistic effect directly on the cells and produce the observed changes in membrane potential. The ventricular arrhythmias observed in digitalized humans or animals that become hypoxemic may result either from the induction of oscillatory after potentials in Purkinje cells causing triggered spontaneous excitations or from reentry of excitation.
研究了缺氧对用哇巴因预处理的离体、灌注纤维束中犬浦肯野细胞跨膜电位的影响。以93次/分钟的频率进行电刺激的细胞暴露于2.1×10⁻⁷M的哇巴因中,直至4期去极化幅度增加到7 - 12mV。未发生心律失常。在10分钟的洗脱期后,应用缺氧溶液(PO₂ = 15 - 50mmHg)2 - 5分钟。这导致最大舒张电位、超射、0期上升速度和动作电位持续时间降低。4期去极化斜率明显增加。在超过90%的实验中出现了以逸搏节律或单发和多发早搏为特征的心律失常。当对正常细胞在相似时间段施加相同水平的缺氧时,未观察到这些变化。用0.3mg/L普萘洛尔阻断β-肾上腺素能受体并没有以任何方式改变经哇巴因预处理的细胞对缺氧的反应,排除了内源性儿茶酚胺的释放对观察到的效应至关重要。这些结果表明,哇巴因和缺氧对细胞有直接协同作用,并产生观察到的膜电位变化。在使用洋地黄化的人类或动物中观察到的低氧血症时发生的室性心律失常,可能是由于浦肯野细胞中振荡后电位的诱导导致触发自发性兴奋,或者是由于兴奋折返。