Hypertension, Vol 14, 111-114, Copyright © 1989 by American Heart Association
RJ Winquist, AL Scott and GP Vlasuk
Intravenous (bolus) administration of endothelin results in a transient
fall in blood pressure that is accentuated in spontaneously hypertensive
rats (SHR) compared with Wistar-Kyoto normotensive rats (WKY). In
attempting to discern possible mechanisms underlying this depressor
response, we examined the ability of endothelin to release atrial
natriuretic factor (ANF) from isolated, spontaneously contracting atria
from SHR and WKY. Isolated right atria were suspended under 3.0 g of
resting force in tissue baths with the amount of immunoreactive ANF (irANF)
released after exposure to endothelin assessed by radioimmunoassay.
Endothelin (10(-8) and 10(-7) M) caused a concentration-dependent increase
(1.5-4.5-fold) in the release of irANF, which was significantly greater in
atria of SHR compared with WKY. The greater release of irANF in atria of
SHR versus WKY was not related to tissue weight or changes in contractile
rate or force induced by endothelin. Therefore, endothelin appears to cause
a direct release of irANF from rat right atria in vitro. As found for the
depressor response in vivo, endothelin is more efficacious in the
hypertensive compared with the normotensive atrial preparation. Release of
ANF may be important in the hypotensive response to endothelin in vivo.
ARTICLES
Enhanced release of atrial natriuretic factor by endothelin in atria from hypertensive rats
Department of Pharmacology, Merck Sharp & Dohme Research Laboratories, West Point, Pennsylvania 19486.
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