Naudascher M, Jaillon P, Lecocq B, Lecocq V, Ferry A, Hilaire J, Maria J F
Unité de Pharmacologie Clinique, Hôpital Saint-Antoine, Paris, France.
J Cardiovasc Pharmacol. 1989 Jul;14(1):1-5. doi: 10.1097/00005344-198907000-00002.
Falipamil (AQ-A 39) is a new verapamil derivative which exerts antitachycardic effects by a direct action on the sinus node. Its effects on heart rate (HR), blood pressure (BP) and ECG intervals were studied in 12 healthy volunteers, at rest and during bicycle exercise tests. In a double-blind, cross-over, single-dose study, the effects of falipamil (100 and 200 mg) during 8-h post-dosing were compared with those of placebo. Falipamil did not modify resting HR, BP, and electrocardiogram (ECG) intervals significantly. Maximal exercise HR significantly decreased by 5.3 +/- 2.9 (SD)% and 11.2 +/- 3.6% 2 h after the 100- and 200-mg dose respectively, whereas placebo had no effect. Exercise BP was not significantly modified by falipamil. The slopes of HR-workload relationships significantly decreased with falipamil. Peak plasma concentrations of falipamil occurred 1-1.5 h after absorption, and the falipamil-induced decrease in exercise HR over 8 h postdosing was proportional to falipamil plasma concentrations. These results suggest that falipamil decreases HR at exercise in normal subjects and may exert antianginal effects in patients with myocardial ischemia.
法利帕米(AQ - A 39)是一种新型维拉帕米衍生物,通过直接作用于窦房结发挥抗心动过速作用。在12名健康志愿者休息时及进行自行车运动试验期间,研究了其对心率(HR)、血压(BP)和心电图间期的影响。在一项双盲、交叉、单剂量研究中,比较了法利帕米(100毫克和200毫克)给药后8小时内与安慰剂的效果。法利帕米对静息时的心率、血压和心电图间期无显著影响。100毫克和200毫克剂量给药后2小时,最大运动心率分别显著降低5.3±2.9(标准差)%和11.2±3.6%,而安慰剂无此作用。法利帕米对运动血压无显著影响。法利帕米使心率 - 工作量关系的斜率显著降低。法利帕米吸收后1 - 1.5小时达到血浆峰浓度,给药后8小时内法利帕米引起的运动心率降低与法利帕米血浆浓度成正比。这些结果表明,法利帕米可降低正常受试者运动时的心率,并可能对心肌缺血患者发挥抗心绞痛作用。