Hypertension, Vol 8, 971-974, Copyright © 1986 by American Heart Association
A Benetos, H Gavras, JM Stewart, RJ Vavrek, S Hatinoglou and I Gavras
This study was designed to examine the contribution of bradykinin to the
depressor effect of different antihypertensive drugs in two-kidney
renovascular hypertensive rats, using a new specific antagonist of
bradykinin. First, the inhibitory capacity of this peptide for exogenously
injected bradykinin (75-200 ng) was tested. An inhibition of the
vasodepressor action of bradykinin by over 50% was found when the
bradykinin inhibitor was infused at a rate of 40 micrograms/min, with
little difference at higher rates of infusion. This inhibitor then was
infused in three groups of renovascular hypertensive rats after their blood
pressure had been decreased by pretreatment with the converting enzyme
inhibitor enalapril (MK 421), saralasin, or sodium nitroprusside,
respectively. Infusion of the inhibitor produced an immediate 30% increase
in blood pressure only in the enalapril-treated group. These results
indicate that bradykinin is involved in the decrease of blood pressure
produced by converting enzyme inhibition in experimental renovascular
hypertension.
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Vasodepressor role of endogenous bradykinin assessed by a bradykinin antagonist
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