Circulation, Vol 81, 308-311, Copyright © 1990 by American Heart Association
RA Mulinari, I Gavras, YX Wang, R Franco and H Gavras
These experiments assessed the hemodynamic and aquaretic effects of an
arginine vasopressin (AVP) antagonist with dual V1V2-receptor inhibiting
properties in rats with congestive heart failure resulting from ischemic
cardiomyopathy. The compound d(CH2)5-D-Tyr(Et)VAVP was used in these
studies. Rats with limited or extensive myocardial infarcts (i.e., with
less than 50% or greater than 66% necrosis of the left ventricular wall,
respectively, induced by left coronary ligation) and sham-operated controls
received the AVP antagonist (100 micrograms/kg i.v.) 4 weeks later. This
agent produced an 18% increase in cardiac output (p less than 0.05) and 13%
decrease in systemic vascular resistance in the severely damaged rats, both
changes being significantly different from those seen in the normal
controls or the rats with limited infarcts. All animals exhibited increases
in urinary output of 4-10-fold over baseline. We conclude that the
hemodynamic and renal effects of this agent are beneficial in animals with
left ventricular dysfunction.
ARTICLES
Effects of a vasopressin antagonist with combined antipressor and antiantidiuretic activities in rats with left ventricular dysfunction
Department of Medicine, Boston University School of Medicine, MA 02118.
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