EFFECTS OF CHRONIC TREATMENT WITH CAPTOPRIL (SQ 14, 225), AN ORALLY ACTIVE INHIBITOR OF ANGIOTENSIN I-CONVERTING ENZYME, IN SPONTANEOUSLY HYPERTENSIVE RATS
The effects of hydralazine (3 mg/kg) and the angiotensin I-converting enzyme (ACE) inhibitor captopril (SQ 14, 225) (100 mg/kg) on mean arterial blood pressure, plasma renin activity, urinary volume and urinary Na+, K+, and aldosterone concentrations were examined in spontaneously hypertensive rats...
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Published in | Japanese journal of pharmacology Vol. 29; no. 2; pp. 285 - 294 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Japan
The Japanese Pharmacological Society
01.01.1979
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Subjects | |
Online Access | Get full text |
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Summary: | The effects of hydralazine (3 mg/kg) and the angiotensin I-converting enzyme (ACE) inhibitor captopril (SQ 14, 225) (100 mg/kg) on mean arterial blood pressure, plasma renin activity, urinary volume and urinary Na+, K+, and aldosterone concentrations were examined in spontaneously hypertensive rats of the Okamoto and Aoki strain (SHR) after oral daily dosing for 2 weeks, 3 or 6 months. Captopril caused progressive cumulative reductions in blood pressure resulting in normalization of pressure after 6 months of dosing. Hydralazine also significantly reduced blood pressure but not to the level of normotensive rats of the Wistar-Kyoto strain (WKY). Reductions in heart size paralleled the changes in blood pressure, normalization of cardiac hypertrophy occurring after captopril but not hydralazine. Plasma renin activity increased approximately 2-3 fold after hydralazine and 15-fold after captopril. Neither hydralazine nor captopril had any consistent effects on 24-hr urine volume, urinary Na+, K+ or aldosterone excretion. These results indicate that chronic inhibition of ACE with captopril induces normalization of blood pressure in SHR, a normal-renin model of hypertension. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 0021-5198 1347-3506 |
DOI: | 10.1254/jjp.29.285 |