Effects of inhibiting neutral endopeptidase and kininase ii on
coronary and systemic hemodynamics in rats.
Maxwell, Andrew J., Waleed K. Husseini, Giovanni Piedimonte, Julien I.
E. Hoffman.
Cardiovascular Research Institute and Department of Pediatrics,
University of California, San Francisco, CA 94143.
APStracts 2:0157H, 1995.
To determine whether neutral endopeptidase (NEP) and kininase II
(angiotensin converting enzyme, ACE) influence coronary hemodynamics,
we compared the effects of inhibiting NEP, ACE, or both before and
after isoproterenol (50 mg/kg i.p.). We measured flow and resistance
using radioactive microspheres in 90 anesthetized rats which received
the NEP inhibitor phosphoramidon (2.5 mg/kg), the ACE inhibitor
captopril (2.5 mg/kg), both combined, or vehicle alone. Before
isoproterenol, inhibiting NEP, ACE or both increased left ventricular
blood flow by 48 +/- 10% (SEM), 33 +/- 9% and 10 +/- 6% respectively,
and decreased left ventricular vascular resistance by 26 +/- 6%, 31
+/- 10%, and 10 +/- 6% respectively. After isoproterenol, NEP
inhibition augmented the decrease in left ventricular vascular
resistance (25 +/- 6% decrease within 90 seconds of isoproterenol vs.
8 +/- 5% in controls). ACE inhibition did not augment the decrease in
resistance but inhibiting both enzymes did so to a lesser extent than
inhibiting NEP. These effects cannot be explained by vascular
responses secondary to changes of myocardial oxygen consumption. We
conclude that NEP and ACE are regulators of myocardial blood flow.
Received 1 March 1994; accepted in final form 24 March 1995.
APS Manuscript Number H196-4.
Article publication pending Am. J. Physiol. (Heart Circ. Physiology).
ISSN 1080-4757 Copyright 1995 The American Physiological Society.
Published in APStracts on 25 April 1995.