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(Circulation. 2002;106:292.)
© 2002 American Heart Association, Inc.
Brief Rapid Communications |
From the Department of Medicine and Therapeutics (C.F., A.S., J.M.) and the Division of Neuroscience and Biomedical Systems (M.M., I.M.), Institute of Biomedical and Life Sciences, University of Glasgow, Scotland, UK; and the Vascular Assessment Group (F.J., C.H.), Caledonian University, Glasgow, Scotland, UK.
Correspondence to Professor J. McMurray, CRI in Heart Failure, Wolfson Building, University of Glasgow, G12 8QQ, Scotland, UK. E-mail j.mcmurray{at}bio.gla.ac.uk
Background It has been shown recently that the pregnancy and parturition hormone, relaxin, is secreted by the heart. This study examined the effects of relaxin in small human resistance arteries from the systemic and pulmonary circulations.
Methods and Results Arteries were obtained from gluteal biopsies and resected lung tissue and studied with the use of wire myography. Cumulative concentration relaxation curves were constructed in systemic arteries with substance P, epoprostenol, atrial natriuretic peptide, and relaxin (concentration range 10-13 -10-7M). The maximal responses were 88(±5)%, 67(±10)%, 52(±16)% and 66(±16)%, respectively. Endothelium removal virtually abolished the action of relaxin. Relaxin had no vasodilator effect in pulmonary arteries.
Conclusions Relaxin is a powerful dilator of systemic resistance arteries secreted by the heart that may contribute to cardiovascular regulation.
Key Words: vasodilation arteries endothelium peptides
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