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Biology of Reproduction, Vol 23, 974-980, Copyright © 1980 by Society for the Study of Reproduction
1 Department of Obstetrics and Gynecology,
St. Louis University School of Medicine,
St. Louis, Missouri 63104 Progesterone production was studied in granulosa cells isolated from the two largest preovulatory follicles of regularly laying White Leghorn hens. oLH (0.1 µg/ml) and dibutyryl cyclic AMP
(BU2 cAMP; 2 mM) stimulated progesterone release after a lag period of 10 and 40 min, respectively. While this "induction" period appeared to be related to the intensity of the stimulus, the
rate of increase in the intracellular content of progesterone was different for the two agonists.
Moreover, dose-response curves during the early phase of steroidogenesis (40 min) were markedly
different from those obtained after 3 h incubation. Under the latter conditions, 50 ng/ml oLH
provoked maximal steroidogenic responses while higher concentrations of the hormone were less
effective. During the early phase, however, maximal stimulation was not observed even at 2 µg/ml
concentrations. When we compared the relative potencies of the two agonists, we found BU2 cAMP
to be more effective than oLH during this early phase but less so after more prolonged incubation
(3h). By employing cycloheximide we demonstrated that continuous protein synthesis is required
for full steroidogenic responses to both oLH and BU2 cAMP. On the other hand actinomycin D was
inhibitory only when present during the first hour. Later addition of this inhibitor actually potentiated the steroidogenic effect of LH. These results are consistent with current concepts of the
mode of action of LH in ovarian cells of mammals.
Note:
ACKNOWLEDGMENTS
This work was supported in part by NIH Grant
HD-09763. Purified oLH was a gift from the Hormone
Distribution Officer, NIH, Bethesda, MD. The experimental birds were generously supplied by Dr. H. V.
Biellier, University of Missouri, Columbia. Miss Janet
Kirchoff provided expert secretarial assistance.
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