1. Renal and Depressor Activities of Inhibitors of Neutral Endopeptidase and Angiotensin Converting Enzyme in Monkeys Infused with Angiotensin II
- Author
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M. M. Asaad, Smith Pl, B.E. Abboa-Offei, Charles R. Dorso, Parker D. Mathers, A A Seymour, and W L Rogers
- Subjects
medicine.medical_specialty ,Angiotensin receptor ,Angiotensin-Converting Enzyme Inhibitors ,Blood Pressure ,Kidney ,chemistry.chemical_compound ,Atrial natriuretic peptide ,Internal medicine ,Renin–angiotensin system ,medicine ,Animals ,Protease Inhibitors ,Cyclic GMP ,Cyclic guanosine monophosphate ,Pharmacology ,Angiotensin II receptor type 1 ,biology ,Angiotensin II ,Sodium ,Angiotensin-converting enzyme ,Benzazepines ,Macaca fascicularis ,Endocrinology ,chemistry ,ACE inhibitor ,biology.protein ,Female ,Neprilysin ,Cardiology and Cardiovascular Medicine ,Atrial Natriuretic Factor ,medicine.drug - Abstract
In a previous study, the depressor activity of combined selective inhibitors of neutral endopeptidase EC 3.4.24.11 (NEP) and angiotensin-converting enzyme (ACE) depended on the level of ACE inhibition, whereas the renal responses were determined by NEP inhibition. Our study confirmed that a mixed NEP/ACE inhibitor BMS-182657 ([S-(R*,R*)]-2,3,4,5-tetrahydro-3-[(2-mercapto-1-oxo-3- phenylpropyl)amino]-2-oxo-1H-benzazepine-1-acetic acid) reduced mean arterial pressure (MAP) when renin release was reduced by a sodium load, suggesting that the depressor response did not require suppression of endogenous angiotensin II generation. Furthermore, a pressor dose of 30 ng/min of angiotensin II was required to block the depressor response to BMS-182657 in the presence or absence of exogenous human atrial natriuretic peptide (hANP 99-126). Thirty ng/min of angiotensin II also significantly enhanced the natriuresis induced by hANP 99-126 after BMS-182657 administration. In contrast, a nonpressor dose of angiotensin II (3 ng/min) reduced basal sodium excretion and the natriuretic responses to exogenous hANP 99-126 in the presence or absence of BMS-182657. The potentiation of the urinary ANP and cyclic guanosine monophosphate (cGMP) responses to hANP 99-126 by BMS-182657 was similar for all doses of angiotensin II; therefore angiotensin did not alter the effects of BMS-182657 on ANP metabolism or cGMP accumulation in the kidney. In summary, the renal responses to mixed metalloprotease inhibitors were apparently mediated by ANP potentiation and were modulated by angiotensin II. The depressor activity depended on ACE inhibition but was not mediated solely by reductions in endogenous angiotensin II levels. more...
- Published
- 1996
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