Abstract

In vertebrates, gonadotropin-releasing hormone (GnRH) represents the primary neuroendocrine link between the brain and the reproductive axis, and in some species up to three different forms of GnRH have been detected. Until recently, it had been assumed that humans and non-human primates only express one form (GnRH-I), but it is now clear they also express a second form (GnRH-II). GnRH-II, like GnRH-I, is highly effective at stimulating gonadotropin release, both in vitro and in vivo, but the neurons that produce GnRH-II are completely distinct from those producing GnRH-I. Moreover, GnRH-II and GnRH-I producing neurons respond very differently to estradiol; specifically, estradiol stimulates GnRH-II gene expression in the former and inhibit GnRH-I gene expression in the latter. Consequently, the negative feedback action of estradiol may be mediated exclusively by the subpopulation of GnRH neurons that express GnRH-I, while the positive feedback action may be mediated exclusively by the subpopulation that expresses GnRH-II. Taken together, these findings raise the possibility that two completely different GnRH neuronal systems participate in the control of primate reproductive physiology. The primary role of GnRH-I neurons is likely to be focused on the maintenance and modulation of tonic pulsatile LH release, whereas the primary role of GnRH-II neurons is likely to be focused on the generation of the preovulatory LH surge. This functional segregation of the primate neuroendocrine reproductive axis lends itself for novel targeted approaches to fertility control and for treatment of human reproductive disorders.

Highlights

  • Reviewed by: Karine Rizzoti, National Institute for Medical Research, UK Anne Barlier, University Aix Marseille, France

  • The ovarian steroid estradiol usually exerts a negative feedback action on gonadotropin-releasing hormone (GnRH) and gonadotropin release, which is epitomized by the marked increases in circulating luteinizing hormone (LH) and follicle-stimulating hormone (FSH) levels that occur at menopause or after ovariectomy

  • The traditional explanation for these two radically different effects of estradiol is that GnRH neurons respond differentially to low and high levels of this sex steroid – negatively when estradiol levels are low and positively when estradiol levels are high

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Summary

Introduction

Show a high level of GnRH-II expression in the hypothalamus as well as in the midbrain (Urbanski et al, 1999; Latimer et al, 2001), which raises the interesting possibility that GnRH-II may contribute to the control of the primate reproductive neuroendocrine axis. Note that a second receptor for GnRH (GnRHR-2) has been cloned in monkeys and humans, but it probably does not have a specific role in controlling the reproductive neuroendocrine axis of primates; in monkeys the GnRHR-2 has a ubiquitous distribution pattern, while in humans there is a stop codon in the middle of its gene sequence which precludes its translation into a functional protein (Cheng and Leung, 2005; Herbison, 2006).

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