Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 1989 Jan;83(1):317-20.
doi: 10.1172/JCI113876.

Integrated cardiac, renal, and endocrine actions of endothelin

Affiliations

Integrated cardiac, renal, and endocrine actions of endothelin

W L Miller et al. J Clin Invest. 1989 Jan.

Abstract

Endothelin, a newly discovered endothelial-derived peptide, has been demonstrated in vitro to have potent vasocontractile properties and has been speculated to play a role in vivo in arterial pressure-volume homeostasis. The present studies in anesthetized dogs were designed to determine the action of endothelin on cardiovascular-renal and endocrine function in vivo as in acute arterial pressure-volume regulation. Intravenous infusion of endothelin (50 ng/kg per min) increases arterial pressure by increasing peripheral vascular resistance but in association with an increase in coronary vascular resistance and decreases in cardiac output. Renal blood flow and glomerular filtration rate were markedly reduced in association with a sustained reduction in sodium excretion and an increase in plasma renin activity. Atrial natriuretic factor, vasopressin, and aldosterone were also elevated. These results indicate that endothelin is a potent vasoconstrictor that elevates systemic blood pressure in association with marked decreases in cardiovascular and renal function. This peptide may function as a counterregulatory hormone to the effects of endothelial-derived vasodilator agent(s).

PubMed Disclaimer

Similar articles

Cited by

References

    1. Nature. 1980 Nov 27;288(5789):373-6 - PubMed
    1. Science. 1986 Mar 7;231(4742):1145-7 - PubMed
    1. Circ Res. 1986 Dec;59(6):663-7 - PubMed
    1. Nature. 1988 Mar 31;332(6163):411-5 - PubMed
    1. Eur J Pharmacol. 1988 May 10;149(3):401-2 - PubMed

Publication types