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Biology of Reproduction, Vol 21, 673-681, Copyright © 1979 by Society for the Study of Reproduction
1 Diabetes Branch, National Institute of Arthritis, Metabolism and Digestive Diseases
National Institutes of Health, Bethesda, Maryland 20014 The biological effects of FSH in the presence and absence of a potent nonsteroidal antiandrogen,
SCH-16423, were investigated in rats to determine if androgens are required for antral follicle
maturation. Treatment of hypophysectomized diethylstilbestrol treated immature female rats with
oFSH for 24 h led to a nine-fold increase in [125I]-hCG binding to isolated granulosa cells and a
marked increase in the ability of cultured granulosa cells to secrete progesterone in vitro when
compared with saline injected controls. Coadministration of SCH-16423 with oFSH for 24 h did
not inhibit the induction of LH/hCG receptors on granulosa cells; progesterone production by
cultured granulosa cells was slightly increased when compared with cells from animals which received FSH alone. When rats were treated with FSH or FSH plus SCH-16423 for 54 h to advance
follicles to the preovulatory stage and subsequently treated with hCG to induce ovulation and
luteinization, it was observed that the antiandrogen potentiated the biological effects of the
gonadotropin as measured by increased ovarian weights and elevated serum progesterone levels
when compared with animals which received only FSH-hCG. These results indicate that androgens
are not required for FSH to initiate antral follicle maturation in vivo and further suggest that
androgens are antagonistic to this process.
2 Reproduction Research Branch, National Institutes of Child Health and Human Development,
National Institutes of Health, Bethesda, Maryland 20014
Note:
ACKNOWLEDGMENTS
We gratefully acknowledge Dr. Leo E. Reichert,
Jr., Department of Biochemistry, Albany Medical
College, Albany, NY 12208 for the gift of oFSH and
hFSH used in these studies.
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