Functional luteolysis in response to hydrogen peroxide in human luteal cells
Author
dc.contributor.author
Vega Vega, Luis Felipe
Author
dc.contributor.author
Carrasco,
Author
dc.contributor.author
Castillo, Andrea
Author
dc.contributor.author
Troncoso, Sofía
Author
dc.contributor.author
Videla, Ximena
Author
dc.contributor.author
Devoto, Luigi
Admission date
dc.date.accessioned
2019-01-29T14:55:19Z
Available date
dc.date.available
2019-01-29T14:55:19Z
Publication date
dc.date.issued
1995
Cita de ítem
dc.identifier.citation
Journal of Endocrinology, Volumen 147, Issue 1, 2018, Pages 177-182
Identifier
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00220795
Identifier
dc.identifier.other
10.1677/joe.0.1470177
Identifier
dc.identifier.uri
https://repositorio.uchile.cl/handle/2250/161333
Abstract
dc.description.abstract
To evaluate the effect of reactive oxygen species in human corpus luteum function, we investigated whether hydrogen peroxide (H2O2) affects the in vitro luteal cell production of steroids. H2O2 treatment (1.0-100 μM) of mid and late luteal cell cultures elicited a dose-dependent decrease in basal progesterone production. However, treatment of mid luteal cells with a low concentration of H2O2 (0.01 μM) significantly stimulated progesterone secretion (P < 0.05). In addition, H2O2 (100 μM) markedly inhibited human chorionic gonadotropin (hCG)-stimulated progesterone and estradiol secretion. cAMP production was enhanced (2.4-fold, P < 0.05) by hCG treatment of luteal cells. The addition of H2O2 (0.1-100 μM) to hCG-stimulated luteal cell cultures elicited a decrease in cAMP concentration (P < 0.05) and in the specific binding of radiolabeled hCG by luteal cells. Progesterone and estradiol production stimulated by dibutyryl cAMP were significantly inhibited by H2O2 (P < 0.05). These findings