Nakamura Y, Akima M, Sakai K
Clin Exp Pharmacol Physiol. 1984 May-Jun;11(3):275-83. doi: 10.1111/j.1440-1681.1984.tb00265.x.
The effects of nicorandil were investigated on ouabain-induced cardiovascular actions in pentobarbitone-anaesthetized dogs. Nicorandil (500 micrograms/kg per h) and ouabain (100 micrograms/kg per h), alone and in combination, were infused intravenously to three groups of dogs. Nicorandil gradually decreased systemic blood pressure, pressure-rate product, left ventricular systolic pressure, and coronary vascular resistance, but did not significantly affect heart rate, left ventricular dP/dt max, coronary blood flow, plasma electrolyte concentrations and ECG patterns. The lethal dose of ouabain was 122 micrograms/kg (s.e.m. = 3, n = 6) and the dose required to elicit ventricular premature beats was 63 micrograms/kg (s.e.m. = 3, n = 6). When nicorandil and ouabain were simultaneously infused intravenously, nicorandil did not affect either the lethal dose of ouabain or the dose required to produce ventricular premature beats, but it significantly inhibited the marked increases in coronary vascular resistance and systemic blood pressure induced by ouabain alone. Even in combination with nicorandil, ouabain maintained its own positive inotropic effect. The results indicate that the combination of ouabain with nicorandil may be beneficial in some conditions of angina pectoris.
研究了尼可地尔对戊巴比妥麻醉犬哇巴因诱导的心血管作用的影响。将尼可地尔(每小时500微克/千克)和哇巴因(每小时100微克/千克)单独及联合静脉输注给三组犬。尼可地尔逐渐降低全身血压、压力-心率乘积、左心室收缩压和冠状血管阻力,但对心率、左心室dP/dt max、冠状动脉血流量、血浆电解质浓度和心电图模式无显著影响。哇巴因的致死剂量为122微克/千克(标准误=3,n=6),引发室性早搏所需剂量为63微克/千克(标准误=3,n=6)。当尼可地尔和哇巴因同时静脉输注时,尼可地尔既不影响哇巴因的致死剂量,也不影响产生室性早搏所需的剂量,但它能显著抑制哇巴因单独诱导的冠状血管阻力和全身血压的显著升高。即使与尼可地尔联合使用,哇巴因仍保持其自身的正性肌力作用。结果表明,哇巴因与尼可地尔联合应用在某些心绞痛情况下可能有益。