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Biology of Reproduction, Vol 22, 307-318, Copyright © 1980 by Society for the Study of Reproduction
1 Department of Physiology, Ralph L. Smith Research Center,
University of Kansas Medical Center,
Kansas City, Kansas 66103 The ovaries of hamsters hypophysectomized (H) on the afternoon of proestrus synthesize
in vitro substantial amounts of progesterone for as long as 20 days post-H (Taya and Greenwald,
1979b). The purpose of the present study was to identify by histochemistry and ultrastructure the
ovarian cell type which still possessed the enzymes capable of steroidogenesis despite the long term
absence of gonadotropins. After Day 6 post-H, the ovaries contained interstitium and viable and atretic small preantral
follicles. The viable preantral follicles were histochemically devoid of A single i.p. injection of 5 µg ovine LH on Day 10, 20 or 30 resulted 3 h later in dramatic
increases in the concentration of serum progesterone and ovarian progesterone and testosterone
but not estradiol-17 These data indicate that the interstitium is an active steroidogenic tissue for at least 30 days
post-H and that LH can rapidly stimulate synthesis and secretion of progesterone and testosterone
by the interstitium in long term hypophysectomized hamsters.
5-3
-hydroxysteroid dehydrogenase (3
-HSDH). Histochemically, there were no appreciable changes in lipids in the
interstitial gland cells (IGC) until Day 20 post-H, followed by a slight decrease by Day 30. The
3
-HSDH activity in the IGC showed no appreciable changes until Day 6 and thereafter decreased
gradually until Day 30. Trace amounts of glucose-6-phosphate dehydrogenase were found in the
IGC until Day 6 and thereafter the enzyme was undetectable. The IGC contained only trace
amounts of acid phosphatase until Day 10, followed by a gradual increase by Day 30.
. Concomitantly, the depletion of lipid droplets in viable interstitial cells was
observed by histochemical and ultrastructural criteria. However, lipid accumulations in degenerating interstitial cells and atretic granulosa cells were unaffected by LH treatment.
Note:
ACKNOWLEDGMENTS
K. T. and S.K.S. were supported as Ford Foundation fellows in reproductive biology. The research
was supported by a grant from NIH (HD00596). We
thank the NIAMDD program of NIH for providing the
ovine LH used in this study.
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