(Hypertension. 2000;36:132.)
© 2000 American Heart Association, Inc.
Scientific Contributions |
From the Department of Medicine & Therapeutics and the Robertson Centre for Biostatistics (N.A.), University of Glasgow, Glasgow, Scotland.
Correspondence to Dr Iain Squire, Department of Medicine & Therapeutics, University of Leicester, Clinical Sciences Building, Leicester LE2 7LX, UK. E-mail is11{at}le.ac.uk
AbstractThe physiological effects of angiotensin-converting enzyme (ACE) inhibition may be in part mediated by bradykinin. We investigated the effect of coadministration of the specific bradykinin B2 receptor antagonist icatibant on hemodynamic and neurohormonal responses to acute intravenous ACE inhibition in normal men on a normal sodium diet. We performed a 4-phase, double-blind, double-dummy, placebo-controlled study in 12 male volunteers. The bradykinin antagonist icatibant (10 mg IV) was coadministered over the first 15 minutes of a 2-hour infusion of the ACE inhibitor perindoprilat (1.5 mg IV). Perindoprilat inhibited ACE activity and elicited the expected changes in active renin concentration and angiotensin peptides. Over the 3 hours after the start of drug infusion, perindoprilat lowered and icatibant increased mean arterial blood pressure (each P<0.0005 versus placebo). Coadministration of icatibant attenuated the mean arterial blood pressure response to perindoprilat (P<0.0005) but had no effect on neurohormonal responses to perindoprilat. Our study indicates that the bradykinin B2 receptor antagonist icatibant attenuates the short-term blood pressurelowering effect of acute ACE inhibition in normal men on a normal sodium diet. Bradykinin B2 receptor antagonism alone increases resting blood pressure. Bradykinin may be involved in the control of blood pressure in the resting state in humans.
Key Words: blood pressure angiotensin-converting enzyme bradykinin icatibant
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