Biol Reprod Email Content Delivery
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by CLARK, J. R.
Right arrow Articles by WOLF, R. C.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by CLARK, J. R.
Right arrow Articles by WOLF, R. C.
Agricola
Right arrow Articles by CLARK, J. R.
Right arrow Articles by WOLF, R. C.

Biology of Reproduction, Vol 25, 332-341, Copyright © 1981 by Society for the Study of Reproduction

Hormonal Regulation of Ovarian Folliculogenesis in Rhesus Monkeys: III. Atresia of the Preovulatory Follicle Induced by Exogenous Steroids and Subsequent Follicular Development

JAMES R. CLARK 1, DONALD J. DIERSCHKE 1, , and RICHARD C. WOLF 1

1 Wisconsin Regional Primate Research Center, University of Wisconsin, Madison, Wisconsin 53706


This experiment was designed to determine the effect of exogenous steroids on the preovulatory follicle and to evaluate subsequent ovarian and pituitary function as related to development of a substitute follicle. The original preovulatory follicle was identified by laparoscopy on Day 6 of the menstrual cycle in 29 monkeys, and Silastic capsules containing cholesterol, estradiol-17beta (E2), or progesterone (P) were implanted s.c. in the following groups of animals: A) one cholesterol capsule for 48 h, B) six E2 capsules for 48 h, C) four E2 capsules for 48 h, D) four E2 capsules for 24 h, E) four E2 plus one P capsule for 48 h, and F) one P capsule for 48 h. Serum concentrations of follicle stimulating hormone (FSH), luteinizing hormone (LH), E2, and P were determined by radioimmunoassay.

As expected, treatment with E2, for 48 h resulted in premature surges of LH and FSH, but no surges were induced with E2 treatment for 24 h or with P treatments. Rather, small increases in FSH (but not LH) were consistently noted following removal of the latter implants. Regardless of the E2 or P treatment used or the response observed in gonadotropmn secretion, serum concentrations of endogenous E2 declined within 36 h after the capsules were implanted, and the preovulatory follicle regressed. In animals receiving cholesterol, hormone profiles were typical of those in normal menstrual cycles and ovulation occurred at the usual time.

Following the FSH increases described above and atresia of the original preovulatory follicle, a different follicle developed and ovulated with normal luteal function ensuing. These extended follicular phases averaged 23.1 days, but the intervals from the FSH increase to ovulation approximated the length of a normal follicular phase (13.5 days in our control animals).

These results indicate that elevated serum concentrations of E2 or P during development of the follicle otherwise destined to ovulate disrupt the preovulatory development and result in atresia; based on declining amounts of estrogen in the peripheral circulation, this effect may be exerted within the first day of treatment. Furthermore, the consistent association between FSH increases and renewed follicular development suggests, but does not prove, a cause and effect relationship between these events.

Note:
ACKNOWLEDGMENTS The authors wish to thank Dr. W. E. Bridson for assaying the samples for LH and FSH and Dr. J. Rutledge for assistance with statistical analysis. They gratefully acknowledge the technical assistance of Robert Abrams, JoAnne Mc Kinlay, Patricia Meller, Joey Meyer, Don Phillips, Mary Jo Toivola, Robert Webber, and the animal care staff.

Submitted on September 30, 1980
Accepted on April 28, 1981







HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 1981 by the Society for the Study of Reproduction.