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Blood pressure, plasma volume, and catecholamine levels during enalapril therapy in blacks with hypertension
Author(s) -
Freier Paul A,
Wollam Gary L,
Hall W Dallas,
Unger Deanne J,
Douglas Margaret B,
Bain Raymond P
Publication year - 1984
Publication title -
clinical pharmacology and therapeutics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.941
H-Index - 188
eISSN - 1532-6535
pISSN - 0009-9236
DOI - 10.1038/clpt.1984.250
Subject(s) - enalapril , blood pressure , hydrochlorothiazide , supine position , medicine , epinephrine , essential hypertension , endocrinology , norepinephrine , catecholamine , angiotensin converting enzyme , anesthesia , dopamine
The effect of enalapril, an antihypertensive inhibitor of angiotensin‐converting enzyme, on plasma catecholamine levels and plasma volume (PV) has not been well established. In a randomized, double‐blind study, 29 subjects (28 blacks and one white) received one of the following dosing regimens: hydrochlorothiazide (HCTZ), 25 mg twice a day (group 1; n = 12); enalapril, 10 mg twice a day (group 2; n = 12); or enalapril, 10 mg twice a day, with HCTZ, 25 mg twice a day (group 3; n = 5). Dosages were doubled after 4 wk if diastolic blood pressure was ≥90 mm Hg. After 8 wk of therapy, supine blood pressure decreased by 24.1/16.0 mm Hg (systolic/diastolic) in group 1, by 10.8/4.0 mm Hg in group 2, and by 48.0/27.8 mm Hg in group 3. Mean values of supine plasma levels of norepinephrine, epinephrine, and dopamine did not change with therapy. PV fell 7.9% in group 1, 1.3% in group 2, and 5.0% in group 3. There were no correlations between changes in PV and blood pressure, but a decrease in PV correlated with an increase in plasma norepinephrine levels in the group treated with HCTZ alone (r = −0.65) and in all 29 subjects combined (r = −0.45). Enalapril alone was not very effective in lowering blood pressure in these subjects, but the combination of enalapril with HCTZ was very effective. There was no evidence of a direct effect of enalapril on the sympathetic nervous system or on PV. Clinical Pharmacology and Therapeutics (1984) 36 , 731–737; doi: 10.1038/clpt.1984.250

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