Abstract
Immature female rats were sacrificed at 0, 4, 8 or 16 h following a single s.c. injection of estradiol-1713 (estradiol, 1 mg). Ovaries from each animal were incubated individually: one in the presence of LH (10 pg/mI) for 4 h, the other with progesterone4-[’4C1 (106 M) for 2 h. For the LH incubated ovaries, in vivo treatment with estradiol had no significant effect on progesterone accumulation, whereas production of both testosterone and androstenedione was inhibited by estradiol in a manner dependent on the duration of estradiol treatment in vivo. Analysis of the conversion of radioactive progesterone to its major metabolites by the contralateral ovaries revealed a time-dependent inhibition by estradiol in the formation of androstenedione, 5n-androstanedione and androsterone, whereas the production of 5n-pregnanedione and 3n-OH-5n-pregnan-20-one was significantly stimulated, also in a time-dependent manner. In another experiment, in vivo stimulation for 1 h with LH produced alterations in the pattern of metabolites of progesterone-4-[’4C1 identical to those found upon treatment with estradiol; both treatments resulted in a marked stimulation of 3n-OH-5n-pregnan-20-one, accompanied by an inhibition, of similar magnitude, of production of androsterone. These results suggest that 1) estradiol may act to inhibit ovarian androgen production by impairing the C170-hydroxylase/C,,20-lyase enzyme systems, thereby diverting C2, -substrates through alternate metabolic pathways leading to accumulation of Snpregnane compounds and 2) the inhibitory action of LH upon ovarian androgen production may be mediated by estrogen.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
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.