Estrogen metabolites in human corpus luteum physiology: differential effects on angiogenic activity.

Soledad Henríquez, Paulina Kohen, Xia Xu, Timothy D Veenstra, Alex Muñoz, Wilder A Palomino, Jerome F Strauss, Luigi Devoto

Journal: Fertility and sterility 2017;106(1):230-237.e1

PMID: 26994433

Abstract

OBJECTIVE

To determine tissue concentrations of E2, estrone, P, and estrogens metabolites (EMs) 2-methoxyestradiol, 2-methoxyestrone, 4-hydroxyestrone, and 16-ketoestradiol in corpus luteum (CL) of different ages, and after hCG administration; and to examine the effects of EMs on vascular endothelial growth factor (VEGF) secretion and angiogenic activity released by cultured luteinizing granulosa cells in the presence and absence of hCG.

DESIGN

Experimental study.

SETTING

University.

PATIENT(S)

Thirty-two healthy women of reproductive age.

INTERVENTION(S)

Corpus luteum was collected at the time of minilaparotomy for tubal sterilization, at varying stages of the luteal phase (LP). Late-LP CL was collected 24 hours after IM administration of 10,000 IU hCG. Granulosa cells were isolated from follicular aspirates obtained from healthy women participating in our IVF program for male factor infertility.

MAIN OUTCOMES MEASURE(S)

Estrogen metabolite concentrations were determined in CL tissue, and VEGF was assessed in conditioned medium. The angiogenic activity was analyzed by bioassay.

RESULT(S)

Concentrations of EMs with proangiogenic activity (16-ketoestradiol and 4-hydroxyestrone) were higher in early and mid-LP CL vs. late-LP CL. These EMs and hCG increased VEGF production and angiogenic activity. Conversely, late-LP CL had significantly higher levels of 2-methoxyestrone and 2-methoxyestradiol, which have antiangiogenic activity. Administration of hCG reduced the production of these EMs.

CONCLUSION(S)

Our findings suggest that the EMs are important paracrine modulators of CL function. Administration of hCG increases the production of EMs with proangiogenic activity and reduces the secretion of those EMs with antiangiogenic action, suggesting a novel mechanism by which the late-LP CL is rescued in conception cycles.

Copyright © 2016 American Society for Reproductive Medicine. All rights reserved.

Address: Institute for Maternal and Child Research, Santiago, Chile.; Research Technology Program, Biomedical Research (formerly SAIC-Frederick), Frederick National Laboratory for Cancer Research, Frederick, Maryland.; Maranatha Baptist University, Watertown, Wisconsin.; Institute for Maternal and Child Research, Santiago, Chile; Department of Obstetrics and Gynecology, Faculty of Medicine, San Borja-Arriaran Clinical Hospital, University of Chile, Santiago, Chile.; Department of Obstetrics and Gynecology, School of Medicine, Virginia Commonwealth University, Richmond, Virginia.; Institute for Maternal and Child Research, Santiago, Chile; Department of Obstetrics and Gynecology, Faculty of Medicine, San Borja-Arriaran Clinical Hospital, University of Chile, Santiago, Chile. Electronic address: [email protected].

Link outs

Subscription / membership required

Bant logo

© Copyright 2026, Nutrition Evidence

NED wishes to thank the following organisations for their support:

We use cookies to improve your experience and analyze site traffic with Google Analytics. By continuing to use our site, you agree to our use of cookies. Learn more.