Kimura S, DeQuattro V, Hernandez P H, Lee D D
University of Southern California School of Medicine, Los Angeles 90033.
Am J Cardiol. 1988 Oct 1;62(10 Pt 1):751-4. doi: 10.1016/0002-9149(88)91216-7.
Celiprolol is a newly developed cardioselective beta-blocking agent with mild beta 2-agonist and weak alpha 2-antagonist properties. To evaluate the acute (2.5 hours) and chronic (2 weeks) effects of celiprolol (400 mg once a day) on plasma renin, aldosterone, norepinephrine and epinephrine, 20 patients with mild to moderate primary hypertension were studied in a double-blind placebo-controlled crossover trial. Two and one-half hours after the first dose of both placebo and celiprolol, supine and standing measurements of blood pressure showed a significant reduction, whereas plasma norepinephrine increases were comparable with baseline values. Placebo and celiprolol produced similar changes on supine blood pressure and plasma norepinephrine. In 9 patients celiprolol decreased plasma renin (from a mean +/- standard deviation of 1.09 +/- 0.35 to 0.77 +/- 0.52 ng/ml/hr, p less than 0.05) and aldosterone (from 9.2 +/- 3.7 to 6.7 +/- 3.9 ng/dl, p less than 0.05) acutely both supine and standing, but placebo did not change these parameters. Celiprolol increased pulse rate supine (but not standing) as compared with baseline values. After 2 weeks of celiprolol therapy, blood pressure was decreased both supine and standing compared with placebo in 18 patients (140 +/- 18/88 +/- 8 vs 149 +/- 18/94 +/- 7, 136 +/- 18/91 +/- 6 vs 142 +/- 20/97 +/- 9 mm Hg, respectively, each p less than 0.05), without a change of pulse rate when supine and with a reduction when standing. There were no significant changes of plasma renin, aldosterone, norepinephrine and epinephrine levels during chronic therapy compared with placebo.
塞利洛尔是一种新开发的具有轻度β₂激动剂和弱α₂拮抗剂特性的心脏选择性β受体阻滞剂。为了评估塞利洛尔(每日一次,400毫克)对血浆肾素、醛固酮、去甲肾上腺素和肾上腺素的急性(2.5小时)和慢性(2周)影响,在一项双盲安慰剂对照交叉试验中对20例轻度至中度原发性高血压患者进行了研究。在服用安慰剂和塞利洛尔的首剂后2.5小时,仰卧位和站立位血压测量均显示显著降低,而血浆去甲肾上腺素的升高与基线值相当。安慰剂和塞利洛尔对仰卧位血压和血浆去甲肾上腺素产生了相似的变化。在9例患者中,塞利洛尔急性地使仰卧位和站立位的血浆肾素(从平均±标准差1.09±0.35降至0.77±0.52纳克/毫升/小时,p<0.05)和醛固酮(从9.2±3.7降至6.7±3.9纳克/分升,p<0.05)降低,但安慰剂未改变这些参数。与基线值相比,塞利洛尔使仰卧位(而非站立位)脉搏率增加。塞利洛尔治疗2周后,18例患者仰卧位和站立位血压均较安慰剂降低(分别为140±18/88±8与149±18/94±7,136±18/91±6与142±20/97±9毫米汞柱,各p<0.05),仰卧位时脉搏率无变化,站立位时脉搏率降低。与安慰剂相比,慢性治疗期间血浆肾素、醛固酮、去甲肾上腺素和肾上腺素水平无显著变化。