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PMID: 2464946 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Analysis of regional responses to endothelin in hindquarters vascular bed of cats.

The American journal of physiology ·Vol. 256 ·No. 2 Pt 2 ·1989-02-00 ·Pages H598-602

Minkes RK, MacMillan LA, Bellan JA, Kerstein MD, McNamara DB, Kadowitz PJ

Abstract

Regional responses to endothelin, a peptide derived from endothelial cells in culture, were investigated in the hindquarters vascular bed of cats, when flow varied naturally and when flow was maintained constant with a pump. Intravenous injections of endothelin at doses of 0.03 and 0.1 nmol/kg caused dose-dependent decreases in systemic arterial pressure and increases in distal aortic blood flow. Injection of endothelin at a dose of 0.3 nmol/kg iv caused a biphasic response characterized by an initial decrease in arterial pressure and an increase in blood flow, which was followed by a secondary rise in pressure and a fall in blood flow. When blood flow to hindquarters was maintained constant with a pump, intra-arterial injection of 0.03 nmol endothelin caused a decrease in perfusion pressure, whereas 0.1-1 nmol doses elicited biphasic responses characterized by an initial decrease followed by a secondary increase in perfusion pressure. When compared with other vasoactive peptides, the pressor activity of endothelin was less than angiotensin II by an order of magnitude but was threefold greater than that of neuropeptide Y in the hindquarters vascular bed. The pressor component of the response to endothelin and the response to the calcium agonist BAY K 8644 were decreased in a reversible manner by nisoldipine, a dihydropyridine calcium entry blocking agent. The results of these studies indicate that porcine-human endothelin has both vasodilator and vasoconstrictor activity in the hindquarters vascular bed of cats. The predominant response at a low concentration is vasodilation, whereas at higher concentrations a vasoconstrictor response that was dependent in part on the influx of extracellular calcium could be demonstrated.(ABSTRACT TRUNCATED AT 250 WORDS)

MeSH Terms
3-Pyridinecarboxylic acid, 1,4-dihydro-2,6-dimethyl-5-nitro-4-(2-(trifluoromethyl)phenyl)-, Methyl ester/pharmacology Angiotensin II/pharmacology Animals Aorta, Abdominal/drug effects,physiology Blood Pressure/drug effects Calcium Channel Blockers/pharmacology Cats Endothelins Endothelium, Vascular/physiology Female Male Neuropeptide Y/pharmacology Nifedipine/analogs & derivatives,pharmacology Nisoldipine Peptides/pharmacology Perfusion Reference Values Regional Blood Flow/drug effects
Chemicals
Calcium Channel Blockers Endothelins Neuropeptide Y Peptides Angiotensin II Nisoldipine 3-Pyridinecarboxylic acid, 1,4-dihydro-2,6-dimethyl-5-nitro-4-(2-(trifluoromethyl)phenyl)-, Methyl ester Nifedipine
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Minkes R K
Department of Pharmacology, Tulane University School of Medicine, New Orleans, Louisiana 70112.
MacMillan L A
Bellan J A
Kerstein M D
McNamara D B
Kadowitz P J
Article Info
Journal
The American journal of physiology
Abbr.
Am J Physiol
ISSN
0002-9513
Published
1989-02-00
Pages
H598-602
Language
English
Region
United States
NLM ID
0370511
Subset
IM
Grants
NHLBI NIH HHS · HL-15580 · United States
NHLBI NIH HHS · HL-18070 · United States
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