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Reduction of resistance artery stiffness by treatment with the AT1-receptor antagonist losartan in essential hypertension
In spontaneously hypertensive rats resistance artery structure, endothelial dysfunction and geometry-independent wall stiffness were reduced by an angiotensin AT1-receptor antagonist. In previous studies of human hypertension, interruption of the renin-angiotensin system corrected small artery struc...
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Published in: | Journal of the renin-angiotensin-aldosterone system 2000-03, Vol.1 (1), p.40-45 |
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Main Authors: | , , |
Format: | Article |
Language: | English |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | In spontaneously hypertensive rats resistance artery structure, endothelial dysfunction and geometry-independent wall stiffness were reduced by an angiotensin AT1-receptor antagonist. In previous studies of human hypertension, interruption of the renin-angiotensin system corrected small artery structure and endothelial dysfunction, whereas the β-blocker atenolol did not. We hypothesized that the AT1R antagonist losartan, but not the β-blocker atenolol, would reduce stiffness of gluteal subcutaneous small arteries in essential hypertensive patients. Seventeen untreated mild essential hypertensive patients (47±2years; 75% male) were randomly assigned in double-blind fashion to losartan or atenolol treatment for one year. Small, resistance size arteries were studied on pressurized myographs. Blood pressure (mmHg) was reduced (p |
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ISSN: | 1470-3203 1752-8976 |
DOI: | 10.3317/jraas.2000.009 |