help button home button Endocrine Society Endocrine Reviews
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS

Endocrine Reviews, doi:10.1210/edrv-7-1-3
Endocrine Reviews 7 (1): 3-10
Copyright © 1986 by The Endocrine Society
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
Right arrow Citation Map
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 Request Copyright Permission
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by CONN, P. M.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by CONN, P. M.

The Molecular Basis of Gonadotropin-Releasing Hormone Action*

P. MICHAEL CONN

Department of Pharmacology, University of Iowa College of Medicine Iowa City, Iowa 52242

Correspondence: Address requests for reprints to: Dr. P. Michael Conn, Department of Pharmacology, University of Iowa, College of Medicine, Iowa City, Iowa, 52240.

Abstract

Introduction: WE HAVE known for more than 15 yr that release of the pituitary gonadotropins (LH and FSH) is regulated by a decapeptide from the hypothalamus, GnRH. This releasing hormone is active in vivo, as well as in pituitary explants, and in cell cultures. Accordingly, it has been possible to obtain a great deal of data which have been used to develop an understanding of GnRH action at the cellular level. Models of GnRH action have been useful to understand and predict the actions of GnRH in vivo and to design means for using the releasing hormone in the treatment of human disorders. The present review will describe our current understanding of GnRH action and serve to update our previous review in this series (1).

Footnotes

* This work was supported in part by NIH Grant HD-19899.




This article has been cited by other articles:


Home page
Proc. Natl. Acad. Sci. USAHome page
M. Lindemans, F. Liu, T. Janssen, S. J. Husson, I. Mertens, G. Gade, and L. Schoofs
Adipokinetic hormone signaling through the gonadotropin-releasing hormone receptor modulates egg-laying in Caenorhabditis elegans
PNAS, February 3, 2009; 106(5): 1642 - 1647.
[Abstract] [Full Text] [PDF]


Home page
Hum ReprodHome page
R.F. Arrais and S.A. Dib
The hypothalamus-pituitary-ovary axis and type 1 diabetes mellitus: a mini review
Hum. Reprod., February 1, 2006; 21(2): 327 - 337.
[Abstract] [Full Text] [PDF]


Home page
Biol. Reprod.Home page
A. Nagy and A. V. Schally
Targeting of Cytotoxic Luteinizing Hormone-Releasing Hormone Analogs to Breast, Ovarian, Endometrial, and Prostate Cancers
Biol Reprod, November 1, 2005; 73(5): 851 - 859.
[Abstract] [Full Text] [PDF]


Home page
Proc. Natl. Acad. Sci. USAHome page
G. Halmos and A. V. Schally
Changes in subcellular distribution of pituitary receptors for luteinizing hormone-releasing hormone (LH-RH) after treatment with the LH-RH antagonist cetrorelix
PNAS, January 22, 2002; 99(2): 961 - 965.
[Abstract] [Full Text] [PDF]


Home page
Proc. Natl. Acad. Sci. USAHome page
M. Kovacs and A. V. Schally
Comparison of mechanisms of action of luteinizing hormone-releasing hormone (LHRH) antagonist cetrorelix and LHRH agonist triptorelin on the gene expression of pituitary LHRH receptors in rats
PNAS, October 9, 2001; 98(21): 12197 - 12202.
[Abstract] [Full Text] [PDF]


Home page
Hum ReprodHome page
T. European Middle East Orgalutran Study Group*
Comparable clinical outcome using the GnRH antagonist ganirelix or a long protocol of the GnRH agonist triptorelin for the prevention of premature LH surges in women undergoing ovarian stimulation
Hum. Reprod., April 1, 2001; 16(4): 644 - 651.
[Abstract] [Full Text] [PDF]


Home page
Endocr. Rev.Home page
U. B. Kaiser, P. M. Conn, and W. W. Chin
Studies of Gonadotropin-Releasing Hormone (GnRH) Action Using GnRH Receptor-Expressing Pituitary Cell Lines
Endocr. Rev., February 1, 1997; 18(1): 46 - 70.
[Abstract] [Full Text]


Home page
Toxicol PatholHome page
J. J. Heindel and K. A. Treinen
Physiology of the Male Reproductive System: Endocrine, Paracrine and Autocrine Regulation
Toxicol Pathol, February 1, 1989; 17(2): 411 - 445.
[Abstract] [PDF]


Home page
Proc. Natl. Acad. Sci. USAHome page
M. Kovacs, A. V. Schally, B. Csernus, and Z. Rekasi
Luteinizing hormone-releasing hormone (LH-RH) antagonist Cetrorelix down-regulates the mRNA expression of pituitary receptors for LH-RH by counteracting the stimulatory effect of endogenous LH-RH
PNAS, February 13, 2001; 98(4): 1829 - 1834.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Endocrinology Endocrine Reviews J. Clin. End. & Metab.
Molecular Endocrinology Recent Prog. Horm. Res. All Endocrine Journals
Copyright © 1986 by The Endocrine Society