Please use this identifier to cite or link to this item: https://repository.monashhealth.org/monashhealthjspui/handle/1/33509
Title: Endothelin and neutral endopeptidase in the endometrium of women with menorrhagia.
Authors: Salamonsen L.A.;Marsh M.M.;Malakooti N.;Taylor N.H.;Findlay J.K.
Institution: (Marsh, Malakooti, Findlay, Salamonsen) Prnc. Henry's Inst. of Med. Research, PO Box 5152, Clayton 3168, Australia (Taylor) Monash University, Department of Obstetrics, Monash Medical Centre, 246 Clayton Road, Clayton, Vic. 3168, Australia
Issue Date: 11-Nov-1997
Copyright year: 1997
Publisher: Oxford University Press
Place of publication: United Kingdom
Publication information: Human Reproduction. 12 (9) (pp 2036-2040), 1997. Date of Publication: 1997.
Journal: Human Reproduction
Abstract: The mechanisms underlying excessive menstrual bleeding or menorrhagia are not understood. In view of its potent vasoconstrictor and growth factor properties, endothelin has been proposed to have a potential paracrine role in the regulation of uterine blood flow and therefore could be a factor in menorrhagia. We compared the cellular localization of endothelin and its metabolizing enzyme, neutral endopeptidase, in endometrial biopsies from women with documented menorrhagia and in those with a normal menstrual cycle. Menorrhagia was documented by measurement of menstual blood loss, 146 +/- 141 ml (median +/- SD). Endothelin and neutral endopeptidase were localized by immunohistochemistry, and the staining intensity was graded. Their immunostaining patterns were found to differ in menorrhagia compared to the normal menstrual cycle. Endothelin was reduced in glandular epithelium in menorrhagia and did not vary cyclically, while neutral endopeptidase was increased in the glandular epithelium. In menorrhagia, stromal endothelin immunoreactivity was not different from the normal cycle and although neutral endopeptidase immunostaining in stroma was similar to the secretory phase of normal endometrium, cyclical variation was absent. The potential for increased metabolism of endothelin could be an explanation for the decreased endothelin immunostaining in the glandular epithelium.
DOI: http://monash.idm.oclc.org/login?url=http://dx.doi.org/10.1093/humrep/12.9.2036
Link to associated publication: Click here for full text options
PubMed URL: 9363725 [http://www.ncbi.nlm.nih.gov/pubmed/?term=9363725]
ISSN: 0268-1161
URI: https://repository.monashhealth.org/monashhealthjspui/handle/1/33509
Type: Article
Subjects: clinical article
controlled study
*endometrium
endometrium biopsy
female
human
human tissue
immunohistochemistry
*menorrhagia/et [Etiology]
menstrual cycle
menstruation
stroma
*endothelin/ec [Endogenous Compound]
*membrane metalloendopeptidase/ec [Endogenous Compound]
cellular distribution
article
menstrual cycle
menstruation
stroma
human tissue
human
female
endometrium biopsy
*endometrium
immunohistochemistry
*menorrhagia / *etiology
controlled study
clinical article
cellular distribution
article
Appears in Collections:Articles

Show full item record

Page view(s)

10
checked on Jul 21, 2024

Google ScholarTM

Check


Items in Monash Health Research Repository are protected by copyright, with all rights reserved, unless otherwise indicated.