17β-Estradiol induces a rapid, endothelium-dependent, sex-specific vasodilatation in spontaneous constricted rat arterioles

Objective: Our purpose was to resolve the apparent contradiction between the endothelium-dependent and endothelium-independent vasodilator effects of 17β-estradiol reported in different studies. Study Design: The inner diameters of isolated pressurized spontaneously constricted muscle arterioles (di...

Full description

Saved in:
Bibliographic Details
Published inAmerican journal of obstetrics and gynecology Vol. 187; no. 2; pp. 375 - 381
Main Authors Smolders, Ramon G.V., van der Mooren, Marius J., Kenemans, Peter, van der Linden, Peter W.J., Stehouwer, Coen D.A., Sipkema, Pieter
Format Journal Article
LanguageEnglish
Published Philadelphia, PA Mosby, Inc 01.08.2002
Elsevier
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:Objective: Our purpose was to resolve the apparent contradiction between the endothelium-dependent and endothelium-independent vasodilator effects of 17β-estradiol reported in different studies. Study Design: The inner diameters of isolated pressurized spontaneously constricted muscle arterioles (diameter = 63 μm) from Wistar rats (n = 21) were measured during exposure to 17β-estradiol, and the role of the endothelium and the influence of sex were assessed. Results: A dose-dependent dilatation was observed during exposure to 17β-estradiol concentrations from 10−10 to 10−4 mol/L. Arterioles of female rats displayed significantly more dilatation than vessels from male rats. The dilatation was significantly less in endothelium-denuded arterioles or after pretreatment with and in the presence of a nitric oxide synthase inhibitor. Conclusions: These results provide strong evidence that, in addition to an endothelium-independent effect, 17β-estradiol has a dose-dependent, endothelium-mediated, rapid vasodilatory effect on muscle arterioles from the rat, which is stronger in female rats than in male rats. (Am J Obstet Gynecol 2002;187:375-81.)
ISSN:0002-9378
1097-6868
DOI:10.1067/mob.2002.123599