Cherchi A, Lai C, Onnis E, Solinas R
Institute of Cardiology, University of Cagliari, Italy.
J Cardiovasc Pharmacol. 1992;20 Suppl 7:S75-82.
Gallopamil (GSR) is a new calcium-channel blocker. The anti-ischemic activity of GSR was investigated in 12 patients with stable angina of effort, with fixed ischemic threshold (variations < 15%). After a 7-day washout period, patients were randomized to receive treatment with either GSR 100 mg or placebo twice daily for 7 days. Patients underwent maximal symptom-limited exercise test, 10 W/min on a bicycle, during washout (twice) and after the end of each treatment period. Patients were studied by electrocardiogram and the cuff method for determining systolic blood pressure. After treatment with GSR, ischemic and anginal thresholds were increased for at least 12 h in comparison with placebo (ischemic threshold: GSR 663 +/- 37, placebo 571 +/- 36, p < 0.01; anginal threshold: GSR 708 +/- 32, placebo 646 +/- 38, p < 0.05). Rate-pressure product was not changed at the same levels of exercise, but it was significantly increased during exercise at ischemic threshold. In conclusion, GSR possesses an anti-ischemic and antianginal activity lasting at least 12 h. This activity seems due to an increase of coronary blood flow to ischemic areas.
加洛帕米(GSR)是一种新型钙通道阻滞剂。对12例劳力性稳定型心绞痛患者进行了GSR抗缺血活性研究,这些患者具有固定的缺血阈值(变化<15%)。经过7天的洗脱期后,患者被随机分为两组,分别接受每日两次100mg GSR或安慰剂治疗,为期7天。患者在洗脱期(两次)以及每个治疗期结束后,进行症状限制最大运动试验,采用自行车运动,速度为每分钟10瓦。通过心电图和袖带法对患者进行研究以测定收缩压。与安慰剂相比,GSR治疗后,缺血阈值和心绞痛阈值至少升高12小时(缺血阈值:GSR为663±37,安慰剂为571±36,p<0.01;心绞痛阈值:GSR为708±32,安慰剂为646±38,p<0.05)。在相同运动水平下,心率-血压乘积未发生变化,但在缺血阈值运动期间显著升高。总之,GSR具有至少持续12小时的抗缺血和抗心绞痛活性。这种活性似乎是由于缺血区域冠状动脉血流量增加所致。