Molecular Human Reproduction Vol. 2, NUMBER 2 pp. 117-121, 1996
© European Society of Human Reproduction and Embryology 1996
research-article |
GnRH receptor mRNA expression by in-situ hybridization in the primate pituitary and ovary
MRC Reproductive Biology Unit, Centre for Reproductive Biology 37 Chalmers Street, Edinburgh EH3 9EW, UK
To whom correspondence should be addressed at: 1To whom correspondence should be addressed
Gonadotrophin-releasing hormone (GnRH) receptors are present on the ovary as well as in the anterior pituitary gland. GnRH analogues may exert their actions in part via these ovarian receptors. However, in the primate ovary, GnRH receptors are of low affinity and their significance is questionable. The aim of the present study was to compare pituitary and ovarian expression of the GnRH receptor mRNA by in-situ hybridization to gain further information on the possible significance of the ovarian receptor. Pituitaries and ovaries were obtained from two stump-tailed macaque monkeys and three marmoset monkeys at the mid-luteal phase of the ovulatory cycle. Human corpora lutea were obtained during the early and mid-luteal phase and after rescue by human chorionic gonadotrophin (HCG) and a whole ovary obtained during the late luteal phase (n=1 per group). Frozen tissue sections were incubated with a 33P-labelled probe to the human GnRH receptor and exposed for 4 weeks. All pituitary glands exhibited intense silver grains in the anterior pituitary gland. In the ovaries, grains were present at low levels in the granulosa cells of antral follicles, just above tissue background in corpora lutea and indistinguishable from tissue background in the remaining ovarian compartments. These results demonstrate that the GnRH receptor mRNA in the primate pituitary is present in sufficient quantities to be clearly detectable in the anterior pituitary gland by in-situ hybridization. In contrast, in the human and monkey, ovary levels of mRNA appear to be very low.
corpus luteum/follicle/GnRH mRNA/in-situ hybridization
![]()
CiteULike
Connotea
Del.icio.us What's this?
This article has been cited by other articles:
![]() |
P. Chen and S. M. Moenter GABAergic Transmission to Gonadotropin-Releasing Hormone (GnRH) Neurons Is Regulated by GnRH in a Concentration-Dependent Manner Engaging Multiple Signaling Pathways J. Neurosci., August 5, 2009; 29(31): 9809 - 9818. [Abstract] [Full Text] [PDF] |
||||
![]() |
C. Metallinou, B. Asimakopoulos, A. Schroer, and N. Nikolettos Gonadotropin-Releasing Hormone in the Ovary Reproductive Sciences, December 1, 2007; 14(8): 737 - 749. [Abstract] [PDF] |
||||
![]() |
C.-S. Chou, H. Zhu, E. Shalev, C. D. MacCalman, and P. C. K. Leung The Effects of Gonadotropin-Releasing Hormone (GnRH) I and GnRH II on the Urokinase-Type Plasminogen Activator/Plasminogen Activator Inhibitor System in Human Extravillous Cytotrophoblasts in Vitro J. Clin. Endocrinol. Metab., December 1, 2002; 87(12): 5594 - 5603. [Abstract] [Full Text] [PDF] |
||||
![]() |
O. Ortmann, J.M. Weiss, and K. Diedrich Embryo implantation and GnRH antagonists: Ovarian actions of GnRH antagonists Hum. Reprod., April 1, 2001; 16(4): 608 - 611. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. E. Dickson and H. M. Fraser Inhibition of Early Luteal Angiogenesis by Gonadotropin-Releasing Hormone Antagonist Treatment in the Primate J. Clin. Endocrinol. Metab., June 1, 2000; 85(6): 2339 - 2344. [Abstract] [Full Text] |
||||
![]() |
H.M. Fraser, S.F. Lunn, D.J. Harrison, and J.B. Kerr Luteal Regression in the Primate: Different Forms of Cell Death During Naturaland Gonadotropin-Releasing Hormone Antagonist or Prostaglandin Analogue-Induced Luteolysis Biol Reprod, December 1, 1999; 61(6): 1468 - 1479. [Abstract] [Full Text] |
||||




