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American Heart Journal

Publication date: 1983-08-01
Volume: 106 Pages: 321 -
Publisher: Elsevier

Author:

Staessen, Jan
Fagard, Robert ; Lijnen, Paul ; Verschueren, LJ ; Amery, A

Keywords:

Bendroflumethiazide, Body Weight, Captopril, Clinical Trials, Double-Blind Method, Drug Resistance, Drug Therapy, Combination, Electrolytes, Female, Humans, Hypertension, Male, Middle Aged, Proline, Propranolol, Prostaglandins, Pulse, Renin-Angiotensin System, Uric Acid, Science & Technology, Life Sciences & Biomedicine, Cardiac & Cardiovascular Systems, Cardiovascular System & Cardiology, Clinical Trials as Topic, 1102 Cardiorespiratory Medicine and Haematology, 1117 Public Health and Health Services, Cardiovascular System & Hematology, 3201 Cardiovascular medicine and haematology

Abstract:

In a double-blind crossover trial, 15 captopril (daily dose 600 mg) treated patients received in addition to the converting enzyme inhibitor, placebo, propranolol (240 mg), or bendroflumethiazide (7.5 mg). Propranolol produced an additional hypotensive effect, while pulse rate slowed, indicating effective beta-adrenoceptor blockade. Plasma renin activity decreased, but the hypotensive effect of propranolol was not accompanied by changes in the plasma angiotensin II and aldosterone levels or in the urinary aldosterone excretion. Also bendroflumethiazide lowered blood pressure, while body weight decreased slightly. During captopril-bendroflumethiazide treatment, serum sodium and potassium decreased while the plasma renin-angiotensin-aldosterone system was stimulated. In these captopril-treated patients, the hypotensive response to bendroflumethiazide tended to be somewhat larger than the response to propranolol, but the difference was small and statistically not significant.