| Literature DB >> 1661764 |
A Erman1, J Winkler, B Chen-Gal, M Rabinov, A Zelykovski, S Tadjer, J Shmueli, E Levi, A Akbary, J B Rosenfeld.
Abstract
Studies in animal models have indicated that ramipril is a potent inhibitor of angiotensin converting enzyme (ACE) in serum and tissue. In our study, the normal range of ACE activity and the inhibitory effect of short-term oral administration of ramipril on ACE activity in human serum and tissue samples of renal cortex, heart and blood vessels were determined. ACE activity in the renal cortex (125.2 +/- 11.5 nmol/mg per min) was greater than 600 times that of the heart (0.20 +/- 0.01 nmol/mg per min), greater than 500 times that of the veins (0.23 +/- 0.09 nmol/mg per min) and greater than 150 times that of the arteries (0.80 +/- 0.23 nmol/mg per min). ACE activity in the renal cortex and arteries 2 h after last dosing was almost completely inhibited by ramipril whereas ACE activity in the veins and heart was inhibited to a lesser extent. Our results demonstrate in man, for the first time, an inhibition of tissue ACE following short-term oral treatment with an ACE inhibitor.Entities:
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Year: 1991 PMID: 1661764 DOI: 10.1097/00004872-199111000-00012
Source DB: PubMed Journal: J Hypertens ISSN: 0263-6352 Impact factor: 4.844