Hongo M, Takenaka H, Uchikawa S, Nakatsuka T, Watanabe N, Sekiguchi M
First Department of Internal Medicine, Shinshu University School of Medicine, Matsumoto, Japan.
Am J Cardiol. 1995 Feb 1;75(4):246-50. doi: 10.1016/0002-9149(95)80029-r.
Nicorandil is an antianginal drug that causes potent coronary vasodilation of both epicardial and resistance vessels. To measure the dose-response kinetics of bolus injections of intracoronary nicorandil and to compare the vasodilatory response to nicorandil with that of intracoronary papaverine in humans, coronary blood flow velocity was measured in 30 patients using a 3Fr intravascular Doppler catheter. Continuous intravenous nitroglycerin 6 to 8 micrograms/min was infused to achieve maximal vasodilation of the epicardial vessels. Bolus doses of nicorandil dissolved in warmed saline solution were injected into the left (0.1, 0.2, 0.5, 1.0, 1.5, and 2.0 mg) and right (0.1, 0.2, 0.4, 0.8, 1.0, and 1.5 mg) coronary arteries. Intracoronary nicorandil caused a dose-dependent increase in coronary flow velocity and a decrease in coronary vascular resistance. Maximal vasodilatory effects equivalent to those obtained with 12 +/- 2 mg of intracoronary papaverine were induced with nicorandil 1.5 mg in the left coronary artery, and effects similar to those of 10 +/- 2 mg of papaverine were produced with nicorandil 1.0 mg in the right coronary artery. The time from injection of nicorandil to the onset of maximal hyperemia and duration of hyperemia were significantly shorter after nicorandil than after papaverine in both coronary arteries. Each dose of nicorandil produced no clinical symptoms and fewer changes in systemic hemodynamics and electrocardiographic QT intervals than did papaverine. These results suggest that a bolus administration of intracoronary nicorandil can safely, quickly, and reliably induce maximal coronary hyperemia comparable to that achieved with intracoronary papaverine in humans.
尼可地尔是一种抗心绞痛药物,可引起心外膜血管和阻力血管的强效冠状动脉扩张。为了测量冠状动脉内注射尼可地尔推注的剂量反应动力学,并比较尼可地尔与冠状动脉内注射罂粟碱在人体中的血管舒张反应,使用3Fr血管内多普勒导管在30例患者中测量了冠状动脉血流速度。持续静脉输注硝酸甘油6至8微克/分钟,以实现心外膜血管的最大扩张。将溶解在温热盐溶液中的尼可地尔推注剂量注入左冠状动脉(0.1、0.2、0.5、1.0、1.5和2.0毫克)和右冠状动脉(0.1、0.2、0.4、0.8、1.0和1.5毫克)。冠状动脉内注射尼可地尔可导致冠状动脉血流速度剂量依赖性增加和冠状动脉血管阻力降低。左冠状动脉注射1.5毫克尼可地尔可诱导出与12±2毫克冠状动脉内注射罂粟碱相当的最大血管舒张作用,右冠状动脉注射1.0毫克尼可地尔可产生与10±2毫克罂粟碱相似的作用。在两条冠状动脉中,注射尼可地尔至最大充血开始的时间和充血持续时间在尼可地尔注射后比罂粟碱注射后明显缩短。与罂粟碱相比,每次尼可地尔剂量产生的临床症状更少,全身血流动力学和心电图QT间期变化也更少。这些结果表明,冠状动脉内推注尼可地尔可以安全、快速且可靠地诱导出与人体冠状动脉内注射罂粟碱相当的最大冠状动脉充血。