Human Reproduction, Vol 12, 1877-1885, Copyright © 1997 by Oxford University Press
MB Zelinski-Wooten, JS Hutchison, I Trinchard-Lugan, DL Hess, DP Wolf and RL Stouffer
During in-vitro fertilization (IVF) cycles, a large bolus of human
chorionic gonadotrophin (HCG) is used to induce periovulatory events, but
the efficacy of lower doses is undefined. Following follicular stimulation
in rhesus monkeys, oocyte nuclear maturation, IVF, granulosa cell
luteinization and corpus luteum function were compared after injection of
100, 300 or 1000 IU recombinant HCG or 1000 IU urinary HCG. Bioactive HCG
rose to peak concentrations within 2 h that were proportional to the dose
administered (100 < 300 < 1000 IU, recombinant HCG = urinary HCG).
The duration of surge values (>100 ng/ml) was also dose-dependent (0 h,
100 IU; 24 h, 300 IU; >48 h, 1000 IU, recombinant and urinary HCG).
While the proportions of oocytes resuming meiosis and undergoing IVF were
similar among groups, fewer animals yielded fertilizable oocytes following
100 and 300 IU (five of nine) compared to 1000 IU recombinant and urinary
HCG (nine of 10). Peak values of serum progesterone in the luteal phase
were similar, but declined 2 days earlier after 100 and 300 IU relative to
1000 IU recombinant and urinary HCG. Thus, 3-10 fold lower doses of HCG
elicit low amplitude surges of short duration that induce periovulatory
events such as re-initiation of oocyte meiosis and granulosa cell
luteinization. However, oocyte fertilization and luteal function may
optimally require surges of higher amplitude and longer duration similar to
those produced by standard doses of 1000 IU recombinant or urinary HCG.
ARTICLES
Initiation of periovulatory events in gonadotrophin-stimulated macaques with varying doses of recombinant human chorionic gonadotrophin
Oregon Regional Primate Research Center, Beaverton 97006, USA.
![]()
CiteULike
Connotea
Del.icio.us What's this?
This article has been cited by other articles:
![]() |
B. L Dozier, K. Watanabe, and D. M Duffy Two pathways for prostaglandin F2{alpha} synthesis by the primate periovulatory follicle Reproduction, July 1, 2008; 136(1): 53 - 63. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. Bloch, Y. Folman, M. Kaim, Z. Roth, R. Braw-Tal, and D. Wolfenson Endocrine Alterations Associated with Extended Time Interval Between Estrus and Ovulation in High-Yield Dairy Cows J Dairy Sci, December 1, 2006; 89(12): 4694 - 4702. [Abstract] [Full Text] [PDF] |
||||
![]() |
H. Al-Inany, M. A. Aboulghar, R. T. Mansour, and M. Proctor Recombinant versus urinary gonadotrophins for triggering ovulation in assisted conception Hum. Reprod., August 1, 2005; 20(8): 2061 - 2073. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. Honaramooz, M.-W. Li, M. C. T. Penedo, S. Meyers, and I. Dobrinski Accelerated Maturation of Primate Testis by Xenografting into Mice Biol Reprod, May 1, 2004; 70(5): 1500 - 1503. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. Kaim, A. Bloch, D. Wolfenson, R. Braw-Tal, M. Rosenberg, H. Voet, and Y. Folman Effects of GnRH Administered to Cows at the Onset of Estrus on Timing of Ovulation, Endocrine Responses, and Conception J Dairy Sci, June 1, 2003; 86(6): 2012 - 2021. [Abstract] [Full Text] [PDF] |
||||
![]() |
T. L. Tollner, J. W. Overstreet, M. W. Li, S. A. Meyers, A. I. Yudin, E. R. Salinas, and G. N. Cherr Lignosulfonic Acid Blocks In Vitro Fertilization of Macaque Oocytes When Sperm Are Treated Either Before or After Capacitation J Androl, November 1, 2002; 23(6): 889 - 898. [Abstract] [Full Text] [PDF] |
||||
![]() |
J.T. Jensen, K.M. Schwinof, M.B. Zelinski-Wooten, M. Conti, L.V. DePaolo, and R.L. Stouffer Phosphodiesterase 3 inhibitors selectively block the spontaneous resumption of meiosis by macaque oocytes in vitro Hum. Reprod., August 1, 2002; 17(8): 2079 - 2084. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. Fritz, I. Wessler, R. Breitling, W. Rossmanith, S. R. Ojeda, G. A. Dissen, A. Amsterdam, and A. Mayerhofer Expression of Muscarinic Receptor Types in the Primate Ovary and Evidence for Nonneuronal Acetylcholine Synthesis J. Clin. Endocrinol. Metab., January 1, 2001; 86(1): 349 - 354. [Abstract] [Full Text] |
||||
![]() |
A. Mayerhofer, S. Fritz, R. Grünert, S. L. Sanders, D. M. Duffy, S. R. Ojeda, and R. L. Stouffer D1-Receptor, DARPP-32, and PP-1 in the Primate Corpus Luteum and Luteinized Granulosa Cells: Evidence for Phosphorylation of DARPP-32 by Dopamine and Human Chorionic Gonadotropin J. Clin. Endocrinol. Metab., December 1, 2000; 85(12): 4750 - 4757. [Abstract] [Full Text] |
||||
![]() |
N. Yesildaglar and P.R. Koninckx Adhesion formation in intubated rabbits increases with high insufflation pressure during endoscopic surgery Hum. Reprod., March 1, 2000; 15(3): 687 - 691. [Abstract] [Full Text] [PDF] |
||||
![]() |
T.M. Hazzard, T.A. Molskness, C.L. Chaffin, and R.L. Stouffer Vascular endothelial growth factor (VEGF) and angiopoietin regulation by gonadotrophin and steroids in macaque granulosa cells during the peri-ovulatory interval Mol. Hum. Reprod., December 1, 1999; 5(12): 1115 - 1121. [Abstract] [Full Text] [PDF] |
||||
![]() |
E.S. Sills, D. P. Levy, M. Moomjy, M. McGee, and Z. Rosenwaks A prospective, randomized comparison of ovulation induction using highly purified follicle-stimulating hormone alone and with recombinant human luteinizing hormone in in-vitro fertilization Hum. Reprod., September 1, 1999; 14(9): 2230 - 2235. [Abstract] [Full Text] [PDF] |
||||
![]() |
C. L. Chaffin, D. L. Hess, and R. L. Stouffer Dynamics of periovulatory steroidogenesis in the rhesus monkey follicle after ovarian stimulation Hum. Reprod., March 1, 1999; 14(3): 642 - 649. [Abstract] [Full Text] [PDF] |
||||
![]() |
D. M. Duffy, D. R. Stewart, and R. L. Stouffer Titrating Luteinizing Hormone Replacement to Sustain the Structure and Function of the Corpus Luteum after Gonadotropin-Releasing Hormone Antagonist Treatment in Rhesus Monkeys J. Clin. Endocrinol. Metab., January 1, 1999; 84(1): 342 - 349. [Abstract] [Full Text] |
||||
![]() |
N. Yesildaglar, J.L. Ordonez, I. Laermans, and P.R. Koninckx The mouse as a model to study adhesion formation following endoscopic surgery: a preliminary report Hum. Reprod., January 1, 1999; 14(1): 55 - 59. [Abstract] [Full Text] [PDF] |
||||






