Please use this identifier to cite or link to this item:
Title: Vasoconstrictor responses are normal but prostanoid-mediated vasodilatation is enhanced in human cirrhotic mesenteric arteries.
Austin Authors: Vaughan, Rhys B ;Angus, James A;Angus, Peter W 
Affiliation: Victorian Liver Transplant Unit, Department of Gastroenterology, Austin Health, Heidelberg, Melbourne, Victoria 3084, Australia
Issue Date: 1-Aug-2005
Publication information: Journal of Gastroenterology and Hepatology; 20(8): 1158-64
Abstract: The mechanisms responsible for mesenteric vasodilatation in cirrhosis have not been fully elucidated. The aim of the present study was to examine whether there is altered intrinsic vascular reactivity of human mesenteric vessels in cirrhosis, which might contribute to vasodilatation in vivo.Ten mesenteric arteries from six cirrhosis patients undergoing liver transplantation were compared with 11 arteries from six control patients. Vasoconstrictor responses to potassium, norepinephrine and methoxamine were determined. Endothelium-dependent vasodilatation responses to acetylcholine and substance P were determined both before and after inhibition of nitric oxide (NO) and prostanoid synthesis.Cirrhotic vessels responded normally to potassium depolarization and did not differ to control vessels with respect to sensitivity and maximal response to norepinephrine. In cirrhotic vessels, inhibition of NO synthesis had significantly less effect on substance P-induced vasorelaxation than in controls (% Relaxation: cirrhosis 70.3 +/- 9.6; control 34.9 +/- 9.5; P = 0.03). However, after inhibition of both NO and prostanoid synthesis, vasodilatory responses were eliminated in both groups.The findings of the present study indicate that intrinsic hyporesponsiveness to vasoconstrictors does not play a pathogenetic role in the mesenteric vasodilatation in human cirrhosis. Furthermore, vasodilator prostanoids might make a significant contribution in mediating enhanced endothelium-dependent vasorelaxation in the mesenteric circulation.
Gov't Doc #: 16048562
DOI: 10.1111/j.1440-1746.2005.03946.x
Type: Journal Article
Subjects: Cardiovascular Agents.pharmacology
Endothelium, Vascular.drug effects.pathology
Enzyme Inhibitors.pharmacology
In Vitro Techniques
Liver Transplantation
Mesenteric Arteries.drug effects.pathology
Middle Aged
Nitric Oxide.antagonists & inhibitors.metabolism.pharmacology
Vasoconstriction.drug effects
Vasoconstrictor Agents.pharmacology
Vasodilation.drug effects
Vasodilator Agents.pharmacology
Appears in Collections:Journal articles

Show full item record

Page view(s)

checked on Dec 7, 2022

Google ScholarTM


Items in AHRO are protected by copyright, with all rights reserved, unless otherwise indicated.