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 HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Terasawa, E.
Right arrow Articles by Schultz, N. J.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Terasawa, E.
Right arrow Articles by Schultz, N. J.
Agricola
Right arrow Articles by Terasawa, E.
Right arrow Articles by Schultz, N. J.

Biology of Reproduction, Vol 31, 732-741, Copyright © 1984 by Society for the Study of Reproduction


ARTICLES

Factors influencing the progesterone-induced luteinizing hormone surge in rhesus monkeys: diurnal influence and time interval after estrogen

E Terasawa, RR Yeoman and NJ Schultz

In the rhesus monkey, progesterone (P) given after a small dose of estradiol benzoate (EB) induces a luteinizing hormone (LH) surge with a short latency and short duration (Terasawa et al., 1982). In the present study, effects of P injection in relation to the interval after EB and to the time of day were investigated. Nine long-term ovariectomized female rhesus monkeys (which were implanted with an estradiol-17 beta (E2) capsule 2 wk prior to the experiments) were injected with EB (10 micrograms) and P (2.5 mg). In order to determine the period of estrogen priming necessary to induce the facilitatory effects of P, P was injected at 30, 24, 12 or 0 h after EB in the first four experiments. The time of EB injections was fixed at 0830 h. To determine whether there is any diurnal influence on the action of P, the EB injection was moved to 2030 h, followed by P 30 h later. Administration of P 30 h after EB induced a typical LH surge with peak latency (6.7 +/- 0.5 h) and duration (16.0 +/- 1.4 h) in all animals. Similarly, P injection 24 h after EB induced a LH surge with peak latency (7.4 +/- 0.4 h) and duration (18.0 +/- 1.2 h) in all animals. The amplitudes of the P-induced LH surges at both 30 h and 24 h after EB were also similar (P 30 h; 65.0 +/- 18.7 ng/ml, P 24 h; 59.8 +/- 24.4 ng/ml). In contrast, administration of P 12 h or 0 h after EB resulted in a LH surge in only 4 and 3 of 9 animals, respectively, and these numbers of responders were significantly less (P 12 h: P=0.0147, P 0 h: P=0.0045) than those of P 30 h and P 24 h. The amplitudes of the LH surge in animals responding to P 12 h and P 0 h after EB were much smaller than those of P 30 and P 24 h after EB (P less than 0.01), although the peak latency and duration of the response were similar. Overall responses to P 12 h and P 0 h after EB were significantly (P less than 0.005) different from those of P 30 h and P 24 h after EB. A 12-h shift of the injection time of both EB and P did not alter the LH response. Reversed timing of EB and P injections induced a LH surge with peak latency, 7.7 +/- 0.5 h; duration, 16.3 +/- 1.7 h; and amplitude, 59.2 +/- 20.7 ng/ml. These results indicate that 1) P injection 24 h or 30 h after EB reliably induces a LH surge with a short latency and duration, 2) P injection 12 h or 0 h after EB is not effective in inducing a LH surge, and 3) there is no diurnal influence on the P-induced LH surge. Therefore, the time interval of estrogen priming required for progesterone action in the rhesus monkey is similar to that required in rodents for LH release as well as for lordosis behavior.(ABSTRACT TRUNCATED AT 400 WORDS)


This article has been cited by other articles:


Home page
EndocrinologyHome page
T. A. Roepke, C. Xue, M. A. Bosch, T. S. Scanlan, M. J. Kelly, and O. K. Ronnekleiv
Genes Associated with Membrane-Initiated Signaling of Estrogen and Energy Homeostasis
Endocrinology, December 1, 2008; 149(12): 6113 - 6124.
[Abstract] [Full Text] [PDF]


Home page
EndocrinologyHome page
T. A. Roepke, A. Malyala, M. A. Bosch, M. J. Kelly, and O. K. Ronnekleiv
Estrogen Regulation of Genes Important for K+ Channel Signaling in the Arcuate Nucleus
Endocrinology, October 1, 2007; 148(10): 4937 - 4951.
[Abstract] [Full Text] [PDF]


Home page
J. Pharmacol. Exp. Ther.Home page
N. K. Mello, J. H. Mendelson, M. Kelly, and C. A. Bowen
The Effects of Cocaine on Basal and Human Chorionic Gonadotropin-Stimulated Ovarian Steroid Hormones in Female Rhesus Monkeys
J. Pharmacol. Exp. Ther., September 1, 2000; 294(3): 1137 - 1145.
[Abstract] [Full Text]


Home page
EndocrinologyHome page
M. Mizuno, M. Gearing, and E. Terasawa
The Role of Neuropeptide Y in the Progesterone-Induced Luteinizing Hormone-Releasing Hormone Surge in Vivo in Ovariectomized Female Rhesus Monkeys
Endocrinology, May 1, 2000; 141(5): 1772 - 1779.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 1984 by the Society for the Study of Reproduction.