Endothelial dysfunction in uterine circulation in preeclampsia: Can estrogens improve it?
Objective: The purpose of this study was to evaluate whether a 3-hour incubation with 17β-estradiol will enhance blood flow- and bradykinin-mediated dilatation and alter pressure-induced basal tone in myometrial resistance arteries from women with preeclampsia and to evaluate the role of nitric oxid...
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Published in | American journal of obstetrics and gynecology Vol. 187; no. 6; pp. 1608 - 1616 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
Philadelphia, PA
Mosby, Inc
01.12.2002
Elsevier |
Subjects | |
Online Access | Get full text |
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Summary: | Objective: The purpose of this study was to evaluate whether a 3-hour incubation with 17β-estradiol will enhance blood flow- and bradykinin-mediated dilatation and alter pressure-induced basal tone in myometrial resistance arteries from women with preeclampsia and to evaluate the role of nitric oxide in the responses that were observed. Study Design: Blood flow- and bradykinin-mediated dilatation and responses to intraluminal pressure of 60 and 80 mm Hg were compared before and after 3 hours of incubation with 17β-estradiol (10−8 mol/L) in isolated myometrial arteries with the pressure myography technique. In separate experiments, the role of nitric oxide on 17β-estradiol-induced responses was evaluated in the presence of the nitric oxide synthase inhibitor (10−4 mol/L). Endothelial morphologic condition was evaluated by scanning electron microscopy. Results: Incubation with 17β-estradiol significantly improved blood flow-mediated dilatation compared with initial blood flow-mediated response in arteries from women with preeclampsia. This effect was nitric oxide mediated, because the nitric oxide synthase inhibitor abolished the response. Arteries from women with preeclampsia demonstrated impaired bradykinin-mediated dilatation compared with that obtained in arteries from normal pregnant women. The 17β-estradiol had no effect on bradykinin-mediated dilatation in arteries from women with preeclampsia. The enhanced pressure-induced tone at 80 mm Hg compared with the tone that developed at 60 mm Hg in arteries from women with preeclampsia was reduced after incubation with 17β-estradiol. This reduction was also nitric oxide mediated. Morphologic signs of endothelial dysfunction were evident in arteries from women with preeclampsia. Conclusion: The 17β-estradiol improved impaired blood flow-mediated dilatation and reduced basal tone through a nitric oxide-mediated pathway in isolated myometrial arteries from women with preeclampsia. (Am J Obstet Gynecol 2002;187:1608-16.) |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 0002-9378 1097-6868 |
DOI: | 10.1067/mob.2002.127378 |