G protein-coupled receptors of the hypothalamic–pituitary–gonadal axis: A case for gnrh, LH, FSH, and GPR54 receptor ligands

✍ Scribed by Laura H. Heitman; Adriaan P. IJzerman

• Publisher: John Wiley and Sons
• Year: 2008
• Tongue: English
• Weight: 438 KB
• Volume: 28
• Category: Article
• ISSN: 0198-6325
• DOI: 10.1002/med.20129

✦ Synopsis

Abstract

The hypothalamic–pituitary–gonadal (HPG) axis, important in reproduction and sex hormone‐dependent diseases, is regulated by a number of G protein‐coupled receptors. The recently “deorphanized” GPR54 receptor activated by the peptide metastin is thought to be the key regulator of the axis, mainly by releasing gonadotropin‐releasing hormone (GnRH) from the hypothalamus. The latter decapeptide, through the activation of the GnRH receptor in the anterior pituitary, causes the secretion of luteinizing hormone (LH) and follicle‐stimulating hormone (FSH), which subsequently activate their respective receptors on the gonadotrope cells. In this review we will discuss the small molecule agonists and antagonists that are currently being developed to intervene with the action of these four receptors. For GnRH receptors, 14 different chemical classes of non‐peptidic antagonists have been reported, while for the LH receptor three classes of agonists have been described. Both agonists and antagonists have been introduced for the FSH receptor. Recently, the first non‐peptidic agonist for GPR54 was reported. © 2008 Wiley Periodicals, Inc. Med Res Rev, 28, No. 6, 975–1011, 2008