Abstract

The secretion of 17β-estradiol (E 2) and the effect of exogenous E 2 on progesterone (P) production by granulosa-luteal cells from 18 women attending an in vitro fertilization (IVF) program were studied. The cells were separated from follicular fluid and precultured in medium containing fetal calf serum. On the third day of culture E 2 (0.25–2.0 μg/ml) was added onto the cells and its effect on both hCG-stimulated and basal P production was measured. E 2 inhibited both basal and hCG-stimulated P production. 1 μg/ml of E 2 caused mean decrements of 55 and 56% in basal and hCG-stimulated P production, respectively. The maximal inhibition by E 2 occurred at 6 hours of incubation, but when the cells were allowed to react with E 2 for longer periods of time the effect became less significant and more variable. At 48 h no inhibition was observed. At 6 h E 2 (1.0 μg/ml) increased both basal and hCG-stimulated pregnenolone production by approx. 10-fold, suggesting that the supression of P production was due to inhibition of 3β-hydroxysteroid dehydrogenase. Exogenous androgen, 5-Androsten-3β-ol-17-one sulfate, dehydroepiandrosterone sulfate (DHEAS), in a dose-dependent manner increased granulosaluteal cell E 2 production. The maximal response was about 1000-fold above the E 2 production of unstimulated cells and was not affected by hCG. However, the maximal amount of E 2 produced was minor in comparison to exogenous doses required for the suppression of P production and did not have the inhibitory effect. It is concluded that the production of E 2 by granulosa-luteal cells is mainly regulated by the availability of androgen substrate, and that E 2 functions as a modulator of luteal P production.

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.