Johnson B F, Romero L, Marwaha R
Clin Pharmacol Ther. 1986 Apr;39(4):389-94. doi: 10.1038/clpt.1986.60.
In an open crossover comparison of propranolol and nitrendipine, 19 patients with hypertension received 40 to 160 mg propranolol and 5 to 20 mg nitrendipine twice a day. Mean (+/- SD) predose supine blood pressure fell from 145/98 +/- 11/7 to 132/88 +/- 12/8 mm Hg with propranolol and to 135/92 +/- 11/9 mm Hg with nitrendipine. Resting heart rate was reduced by propranolol but was unchanged 12 hours after nitrendipine dosing. Neither propranolol nor nitrendipine altered plasma glucose or insulin after oral glucose. Propranolol significantly increased fasting triglyceride levels and reduced high-density lipoprotein cholesterol levels, but nitrendipine induced no change. Propranolol reduced and nitrendipine increased plasma renin activity after exercise. Peak plasma nitrendipine levels were dose proportional and occurred at 1 to 2 hours after dosing, whereas peak blood pressure reductions occurred 4 hours after the last dose of nitrendipine and were associated with mean increases in heart rate. Nitrendipine is almost equivalent in hypotensive effect to propranolol, but nitrendipine increases plasma renin activity after exertion and may produce transient tachycardia. However, nitrendipine does not cause unwanted metabolic effects.
在一项普萘洛尔与尼群地平的开放性交叉对照试验中,19例高血压患者每日两次服用40至160毫克普萘洛尔和5至20毫克尼群地平。服用普萘洛尔后,平均(±标准差)给药前仰卧血压从145/98±11/7毫米汞柱降至132/88±12/8毫米汞柱;服用尼群地平后降至135/92±11/9毫米汞柱。普萘洛尔可降低静息心率,但尼群地平给药12小时后心率无变化。口服葡萄糖后,普萘洛尔和尼群地平均未改变血浆葡萄糖或胰岛素水平。普萘洛尔显著升高空腹甘油三酯水平并降低高密度脂蛋白胆固醇水平,但尼群地平未引起变化。运动后,普萘洛尔降低而尼群地平升高血浆肾素活性。尼群地平血浆峰值水平与剂量成正比,给药后1至2小时出现,而最大血压降幅出现在最后一剂尼群地平给药后4小时,并伴有心率平均升高。尼群地平的降压效果与普萘洛尔几乎相当,但尼群地平运动后会升高血浆肾素活性,并可能产生短暂性心动过速。然而,尼群地平不会引起不良代谢效应。