ABSTRACT
To determine whether the decrease in ovarian 5 alpha-reduced androgen production before first ovulation might be caused by an increase in serum LH, prepuberal female rats were injected at 28-31 days of age with low doses of human chorionic gonadotrophin (hCG) (0.05-0.075 i.u., four times daily). This treatment resulted in ovulation of six to ten ova per rat on day 32 in all animals. Treatment with hCG resulted in a gradual decrease in ovarian content and production (i.e. content in ovary and medium after 4h of incubation) of 5 alpha-dihydrotestosterone (DHT) and 5 alpha-androstane-3 alpha, 17 beta-diol. The ovarian content of DHT and the production of 5 alpha-androstane-3 alpha, 17 beta-diol decreased within 24 h after the first injection of hCG. Oestradiol content and production increased between 24 and 48 h after the start of treatment and was maximal on day 31 (day of pro-oestrus). Activities of 5 alpha-reductase and aromatase were measured in ovarian homogenates obtained on days 29-31. Activity of 5 alpha-reductase in hCG-treated rats was lower than that in control rats on all days studied. Aromatase activity in hCG-treated rats increased between days 29 and 31. It was concluded that multiple injections of low doses of hCG, which may induce ovulation, cause a decrease in 5 alpha-reduced androgen production, which is probably due to a decrease in 5 alpha-reductase activity. The subsequent increase in oestradiol production corresponds with an increase in aromatase activity.(ABSTRACT TRUNCATED AT 250 WORDS)
Subject(s)
Androgens/biosynthesis , Dihydrotestosterone/biosynthesis , Ovary/metabolism , Sexual Maturation , Androstane-3,17-diol/analogs & derivatives , Androstane-3,17-diol/biosynthesis , Animals , Aromatase/metabolism , Cholestenone 5 alpha-Reductase , Chorionic Gonadotropin/pharmacology , Estradiol/biosynthesis , Female , Ovary/enzymology , Ovulation Induction , Oxidoreductases/metabolism , Proestrus , Rats , Rats, Inbred Strains , Time FactorsABSTRACT
Serum LH changes in response to LH-RH injection were measured in intact and ovariectomized, steroid-treated female rats which were androgenized neonatally with 1,250 microgram testosterone propionate (TP) on day 5. At a dose of 20 ng LH-RH/100 g b.w., serum LH levels in intact rats increased over pre-injection levels, and at a dose of 100 ng LH-RH/100 g b.w., LH concentrations 15 min after injection were higher in nembutal-blocked proestrous rats than in androgen-sterilized rats. However, the ovulation response was not different between the groups. In ovariectomized estradiol benzoate (EB)-treated, androgen-sterilized rats, serum LH concentrations 15 and 60 min after LH-RH injection were lower than in similarly treated control rats. This effect was not secondary to the anovulatory state of the animal, since it also occurred in ovariectomized EB-treated prepuberal rats and in rats ovariectomized prepuberally and treated with EB in adulthood. Also, after treatment with 5alpha-dihydrotestosterone propionate (5alpha-DHTP), pituitary responsiveness to LH-RH in androgen-sterilized rats was lower than in control rats, which suggests that the subnormal response in the estrogen-treated rats was not due to a relative insensitivity to estrogen in the androgen-sterilized rats. The relatively high pituitary responsiveness to LH-RH in intact androgen-sterilized rats is probably due to the high circulating estrogen levels. The subnormal pituitary responsiveness to LH-RH after ovariectomy and estradiol treatment suggests, in addition to an effect on the hypothalamus, also a direct effect of neonatal androgen administration on the pituitary.
