Kirch W, Santos S R, Geller M, Mönig H, Stenzel J, Ohnhaus E E
I. Medizinische Klinik, Christian-Albrechts-Universität, Federal Republic of Germany.
Cardiovasc Drugs Ther. 1988 Jul;2(2):205-9. doi: 10.1007/BF00051235.
Following randomized allocation eight healthy volunteers were treated for 1 week each with metoprolol alone (100 mg twice daily), verapamil 80 mg three times a day plus metoprolol 100 mg twice daily, and with nitrendipine 20 mg twice daily. Plasma levels and urinary recovery of the beta-blocker, antipyrine clearance, and heart rate on exercise were measured. Verapamil and nitrendipine slightly prolonged elimination half-life of metoprolol. The urinary recovery of the parent beta-blocker and of its alpha-hydroxy metabolite was elevated by both calcium antagonists (verapamil and nitrendipine). Exercise tachycardia (150 beats/min without drugs) was inhibited more pronounced on the combination therapies than under metoprolol administration alone. Results of the present study indicate that calcium antagonists enhance inhibition of exercise tachycardia caused by metoprolol, possibly due to their binding to myocardial beta-adrenergic receptors which is known from the literature. As both calcium antagonists did not increase plasma levels of metoprolol, in the present study a kinetic interaction between the beta-blocker and the calcium channel blockers investigated does not appear to be responsible for the pharmacodynamic effects observed.
八名健康志愿者经随机分配后,分别接受为期1周的单独美托洛尔治疗(100mg,每日两次)、维拉帕米80mg每日三次加美托洛尔100mg每日两次,以及尼群地平20mg每日两次的治疗。测量了β受体阻滞剂的血浆水平和尿回收率、安替比林清除率以及运动时的心率。维拉帕米和尼群地平均略微延长了美托洛尔的消除半衰期。两种钙拮抗剂(维拉帕米和尼群地平)均使母体β受体阻滞剂及其α-羟基代谢产物的尿回收率升高。联合治疗对运动性心动过速(无药物时为150次/分钟)的抑制作用比单独使用美托洛尔时更为明显。本研究结果表明,钙拮抗剂增强了美托洛尔对运动性心动过速的抑制作用,这可能是由于它们与心肌β-肾上腺素能受体结合,这在文献中已有记载。由于两种钙拮抗剂均未提高美托洛尔的血浆水平,因此在本研究中,所研究的β受体阻滞剂与钙通道阻滞剂之间的动力学相互作用似乎并非观察到的药效学效应的原因。