Estrogen metabolites in human corpus luteum physiology: differential effects on angiogenic activity
Author
dc.contributor.author
Henríquez, Soledad
Author
dc.contributor.author
Kohen Skop, Paulina
Author
dc.contributor.author
Xu, Xia
Author
dc.contributor.author
Veenstra, Timothy D.
Author
dc.contributor.author
Muñoz, Alex
Author
dc.contributor.author
Palomino Avilés, Wilder
Author
dc.contributor.author
Strauss, Jerome F.
Author
dc.contributor.author
Devoto, Luigi
Admission date
dc.date.accessioned
2019-03-18T11:54:13Z
Available date
dc.date.available
2019-03-18T11:54:13Z
Publication date
dc.date.issued
2016
Cita de ítem
dc.identifier.citation
Fertility and Sterility, Vol. 106 No. 1 / July 2016
Identifier
dc.identifier.issn
15565653
Identifier
dc.identifier.issn
00150282
Identifier
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10.1016/j.fertnstert.2016.03.003
Identifier
dc.identifier.uri
https://repositorio.uchile.cl/handle/2250/166757
Abstract
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Objective: To determine tissue concentrations of E2, estrone, P, and estrogensmetabolites (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.