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奈必洛尔与阿替洛尔对原发性高血压的降压及β1-肾上腺素能受体拮抗作用比较

Comparison of antihypertensive and beta 1-adrenoceptor antagonist effect of nebivolol and atenolol in essential hypertension.

作者信息

Simon G, Johnson M L

机构信息

Department of Medicine, Veterans Administration Medical Center, Minneapolis, MN.

出版信息

Clin Exp Hypertens. 1993 May;15(3):501-9. doi: 10.3109/10641969309041625.

Abstract

dl-nebivolol is a new, chemically unique, selective beta 1-adrenoceptor antagonist, without sympathomimetic activity. In the present study, the antihypertensive and negative chronotropic effects of 5 and 10 mg once-daily nebivolol were compared to those of 50 and 100 mg once-daily atenolol in 25 white, male subjects with essential hypertension, using a double-blind, crossover design, and a parallel placebo-treated group of subjects (N = 7). 24 hours after dosing, sitting and standing diastolic and systolic blood pressures and heart rates (at rest and during submaximal exercise) were reduced to the same extent by nebivolol and atenolol. On a weight-for-weight basis, nebivolol is ten times more potent than atenolol. Nebivolol and atenolol also reduced 1-hour ambulatory plasma renin activity. Once-daily nebivolol is an effective antihypertensive beta-adrenoceptor antagonist.

摘要

右旋奈必洛尔是一种新型的、化学结构独特的选择性β1肾上腺素能受体拮抗剂,无拟交感活性。在本研究中,采用双盲、交叉设计以及一组平行的安慰剂治疗组受试者(N = 7),对25名患有原发性高血压的白人男性受试者,比较了每日一次服用5毫克和10毫克奈必洛尔与每日一次服用50毫克和100毫克阿替洛尔的降压和负性变时作用。给药24小时后,奈必洛尔和阿替洛尔使坐位和立位的舒张压和收缩压以及心率(静息时和次极量运动时)降低到相同程度。按重量计算,奈必洛尔的效力是阿替洛尔的10倍。奈必洛尔和阿替洛尔还降低了1小时动态血浆肾素活性。每日一次服用奈必洛尔是一种有效的降压β肾上腺素能受体拮抗剂。

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