Thomas S H, Cooper R C, Ekwuru M, Fletcher S, Gilbody J, Husseyin T S, Ishaque M, Jagathesan R, Reddy G, Smith S E
Division of Pharmacological Sciences and Toxicology, United Medical School, London, UK.
Eur J Clin Pharmacol. 1992;42(1):47-53. doi: 10.1007/BF00314919.
We have evaluated Sramek's method of impedance cardiography as a non-invasive way of detecting the cardiovascular effects of drugs. We made cardiovascular measurements using the method during passive tilting and exercise 2 h after the oral administration of atenolol (50 and 100 mg), propranolol (40 and 80 mg), pindolol (5 and 10 mg), and placebo in seven separate studies involving eight healthy male volunteers. Equivalent doses of the pure antagonists atenolol (beta 1) and propranolol (beta 1, beta 2) produced similar reductions in heart rate, systolic blood pressure, and cardiac index, and increases in stroke volume and total peripheral resistance, particularly during exercise. In contrast the partial agonist pindolol produced increases in heart rate and cardiac index, and reductions in peripheral resistance at rest. During passive tilting and exercise pindolol reduced heart rate, but cardiac output and total peripheral resistance were unchanged except at the highest levels of exercise. The similar cardiovascular effects of atenolol and propranolol, but differing effects of pindolol, are consistent with reports using other methods of measurement. This suggests that impedance cardiography may have a place in the non-invasive assessment of the cardiovascular effects of drugs.
我们评估了斯拉梅克的阻抗心动描记法,将其作为一种检测药物心血管效应的非侵入性方法。在七项分别涉及八名健康男性志愿者的研究中,我们在口服阿替洛尔(50毫克和100毫克)、普萘洛尔(40毫克和80毫克)、吲哚洛尔(5毫克和10毫克)以及安慰剂2小时后,通过该方法在被动倾斜和运动期间进行心血管测量。等效剂量的纯拮抗剂阿替洛尔(β1)和普萘洛尔(β1、β2)使心率、收缩压和心脏指数有相似程度的降低,使每搏量和总外周阻力增加,尤其是在运动期间。相比之下,部分激动剂吲哚洛尔在静息时使心率和心脏指数增加,外周阻力降低。在被动倾斜和运动期间,吲哚洛尔使心率降低,但心输出量和总外周阻力除在最高运动水平外保持不变。阿替洛尔和普萘洛尔相似的心血管效应,但吲哚洛尔的效应不同,这与使用其他测量方法的报告一致。这表明阻抗心动描记法在药物心血管效应的非侵入性评估中可能占有一席之地。