De Servi S, Ferrario M, Ghio S, Mussini A, Angoli L, Bramucci E, Bartoli A, Poma E, Rondanelli R, Specchia G
Br Heart J. 1987 Mar;57(3):226-31. doi: 10.1136/hrt.57.3.226.
The effects of short term intravenous administration of gallopamil on coronary haemodynamic variables were studied in 10 patients with stable exertional angina and angiographically confirmed coronary artery disease that affected the proximal portion of the left anterior descending artery. Blood flow in the great cardiac vein was measured by a thermodilution technique, both at rest and during ischaemia induced by atrial pacing, before and after intravenous administration of gallopamil (0.02 mg/kg as a bolus dose given over three minutes, followed by an infusion of 0.0005 mg/kg/min). Gallopamil significantly prolonged the mean (SD) duration of pacing that was tolerated (11 (2.6) vs 14.8 (2.4] min, significantly increased the mean (SD) peak heart rate attained during pacing (142 (15) vs 158 (11) beats/min), and reduced mean (SD) arterial pressure (133 (17) vs 116 (17) mm Hg). There were no changes in mean (SD) blood flow in the great cardiac vein (134.1 (57) vs 112.9 (38) ml/min, mean (SD) anterior regional coronary resistance (1.18 (0.6) vs 1.15 (0.5) mm Hg/ml/min), and mean (SD) anterior regional myocardial oxygen consumption (16.6 (6) vs 13.7 (4) ml/min). These data confirm that gallopamil is an effective antianginal agent and suggest that a reduction of myocardial oxygen demand is the predominant mechanism by which the drug exerts its beneficial effects.
在10例稳定型劳力性心绞痛且经血管造影证实冠状动脉疾病累及左前降支近端的患者中,研究了短期静脉注射加洛帕米对冠状动脉血流动力学变量的影响。采用热稀释技术测量了大心静脉在静息时以及心房起搏诱发缺血时的血流,测量时间为静脉注射加洛帕米(0.02mg/kg推注剂量,3分钟内给予,随后以0.0005mg/kg/min的速度输注)前后。加洛帕米显著延长了可耐受的起搏平均(标准差)持续时间(11(2.6)分钟对14.8(2.4)分钟),显著增加了起搏期间达到的平均(标准差)峰值心率(142(15)次/分钟对158(11)次/分钟),并降低了平均(标准差)动脉压(133(17)mmHg对116(17)mmHg)。大心静脉的平均(标准差)血流(134.1(57)ml/min对112.9(38)ml/min)、平均(标准差)前降支区域冠状动脉阻力(1.18(0.6)mmHg/ml/min对1.15(0.5)mmHg/ml/min)以及平均(标准差)前降支区域心肌耗氧量(16.6(6)ml/min对13.7(4)ml/min)均无变化。这些数据证实加洛帕米是一种有效的抗心绞痛药物,并表明降低心肌需氧量是该药物发挥有益作用的主要机制。