Mentley R K, Brezinski M E, Tse E, Lefer A M
Department of Physiology, Jefferson Medical College, Thomas Jefferson University, Philadelphia, PA 19107.
Am Heart J. 1988 May;115(5):948-54. doi: 10.1016/0002-8703(88)90062-2.
Nisoldipine, a dihydropyridine with calcium channel-blocking activity, was studied in myocardial ischemia and reperfusion in cats. At an infusion rate of 3 micrograms/kg/hr, nisoldipine did not significantly alter the product of mean arterial blood pressure and heart rate, the pressure-rate index. When infusion of nisoldipine was started 30 minutes after occlusion and continued for 5 1/2 hours, nisoldipine exerted a marked antiischemic effect. This effect was manifested as a significant reduction in necrotic myocardial tissue expressed either as a percentage of area at risk (p less than 0.01) or as a percentage of total left ventricle (p less than 0.01). The washout of creatine kinase into the circulation was also reduced in nisoldipine-treated cats. When nisoldipine infusion started at 60 minutes after ischemia, the effects were still significant (p less than 0.05) but less striking, and when nisoldipine infusion was delayed until 90 minutes after ischemia, no significant cardioprotection was observed. Nisoldipine also blunted the washout of creatine kinase into the peripheral circulation on reperfusion. Thus nisoldipine exerts a cardioprotective effect in cats during myocardial ischemia independent of reducing myocardial oxygen demand. The effect is optimal when nisoldipine is given during the first 30 minutes of ischemia and declines thereafter, reaching insignificant effects at 90 minutes.
尼索地平是一种具有钙通道阻滞活性的二氢吡啶,对猫的心肌缺血和再灌注情况进行了研究。以3微克/千克/小时的输注速率给药时,尼索地平不会显著改变平均动脉血压与心率的乘积,即压力-心率指数。在闭塞后30分钟开始输注尼索地平并持续5个半小时,尼索地平发挥了显著的抗缺血作用。这种作用表现为坏死心肌组织显著减少,无论是以危险区域面积的百分比表示(p<0.01),还是以左心室总面积的百分比表示(p<0.01)。在接受尼索地平治疗的猫中,肌酸激酶释放入循环的情况也有所减少。当在缺血60分钟后开始输注尼索地平,效果仍然显著(p<0.05),但不太明显;当尼索地平输注延迟至缺血90分钟后,未观察到显著的心脏保护作用。尼索地平还减弱了再灌注时肌酸激酶释放入外周循环的情况。因此,尼索地平在猫心肌缺血期间发挥心脏保护作用,且与降低心肌需氧量无关。在缺血的前30分钟内给予尼索地平,效果最佳,此后效果逐渐减弱,至90分钟时作用不明显。