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SAT-423 The Involvement of GnRH Neurons in Mediating the Effects of RFRP-3 on the Mouse Reproductive Axis

In 2000, gonadotrophin-inhibitory hormone was discovered in birds and shown to inhibit gonadotrophin secretion. The mammalian ortholog was concurrently discovered in humans and rats and termed RFamide-related peptide-3 (RFRP-3). Recent results have shown that the effects of centrally-administered RF...

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Autores principales: Ancel, Caroline, Plate, Mathilda, Inglis, Megan, Anderson, Greg
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Endocrine Society 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6552017/
http://dx.doi.org/10.1210/js.2019-SAT-423
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author Ancel, Caroline
Plate, Mathilda
Inglis, Megan
Anderson, Greg
author_facet Ancel, Caroline
Plate, Mathilda
Inglis, Megan
Anderson, Greg
author_sort Ancel, Caroline
collection PubMed
description In 2000, gonadotrophin-inhibitory hormone was discovered in birds and shown to inhibit gonadotrophin secretion. The mammalian ortholog was concurrently discovered in humans and rats and termed RFamide-related peptide-3 (RFRP-3). Recent results have shown that the effects of centrally-administered RFRP-3 on gonadotrophin secretion are sex- and cycle stage-dependent in mice (Ancel et al., 2017). Indeed, intracerebroventricular injections of RFRP-3 stimulated LH secretion in males, and inhibited LH secretion in females at the time of the preovulatory LH surge. In addition, the stimulatory effect observed in males was shown to be mediated in part by GPR54, the receptor for Kisspeptins, suggesting the involvement of other pathways. In order to further our understanding of the ways in which RFRP neurons modulate the reproductive axis, we have developed a novel transgenic mouse line. Using a Cre-loxP conditional transgenic method, we knocked the receptor for RFRP-3 (GPR147) out of GnRH neurons and analysed puberty onset in these mice. While the absence of GPR147 on GnRH neurons advanced puberty onset in male mice, it resulted in a delay in female puberty, once again indicating a sex-specific role of the RFRP system in the regulation of the reproductive function. Current work is aimed at dissecting the potential involvement of GnRH neurons in the pathways mediating RFRP-3 effects on LH secretion in mice carrying a deletion of GPR147 in GnRH neurons. Both male and female mice received intracerebroventricular injections of RFRP-3 and LH levels were subsequently assayed in tail-tip blood samples. This work is still ongoing. Taken together, these new tools provide us with the possibility to advance our understanding of the structure and the functions of the RFRP neuronal system in mice.
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spelling pubmed-65520172019-06-13 SAT-423 The Involvement of GnRH Neurons in Mediating the Effects of RFRP-3 on the Mouse Reproductive Axis Ancel, Caroline Plate, Mathilda Inglis, Megan Anderson, Greg J Endocr Soc Neuroendocrinology and Pituitary In 2000, gonadotrophin-inhibitory hormone was discovered in birds and shown to inhibit gonadotrophin secretion. The mammalian ortholog was concurrently discovered in humans and rats and termed RFamide-related peptide-3 (RFRP-3). Recent results have shown that the effects of centrally-administered RFRP-3 on gonadotrophin secretion are sex- and cycle stage-dependent in mice (Ancel et al., 2017). Indeed, intracerebroventricular injections of RFRP-3 stimulated LH secretion in males, and inhibited LH secretion in females at the time of the preovulatory LH surge. In addition, the stimulatory effect observed in males was shown to be mediated in part by GPR54, the receptor for Kisspeptins, suggesting the involvement of other pathways. In order to further our understanding of the ways in which RFRP neurons modulate the reproductive axis, we have developed a novel transgenic mouse line. Using a Cre-loxP conditional transgenic method, we knocked the receptor for RFRP-3 (GPR147) out of GnRH neurons and analysed puberty onset in these mice. While the absence of GPR147 on GnRH neurons advanced puberty onset in male mice, it resulted in a delay in female puberty, once again indicating a sex-specific role of the RFRP system in the regulation of the reproductive function. Current work is aimed at dissecting the potential involvement of GnRH neurons in the pathways mediating RFRP-3 effects on LH secretion in mice carrying a deletion of GPR147 in GnRH neurons. Both male and female mice received intracerebroventricular injections of RFRP-3 and LH levels were subsequently assayed in tail-tip blood samples. This work is still ongoing. Taken together, these new tools provide us with the possibility to advance our understanding of the structure and the functions of the RFRP neuronal system in mice. Endocrine Society 2019-04-30 /pmc/articles/PMC6552017/ http://dx.doi.org/10.1210/js.2019-SAT-423 Text en Copyright © 2019 Endocrine Society https://creativecommons.org/licenses/by-nc-nd/4.0/ This article has been published under the terms of the Creative Commons Attribution Non-Commercial, No-Derivatives License (CC BY-NC-ND; https://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Neuroendocrinology and Pituitary
Ancel, Caroline
Plate, Mathilda
Inglis, Megan
Anderson, Greg
SAT-423 The Involvement of GnRH Neurons in Mediating the Effects of RFRP-3 on the Mouse Reproductive Axis
title SAT-423 The Involvement of GnRH Neurons in Mediating the Effects of RFRP-3 on the Mouse Reproductive Axis
title_full SAT-423 The Involvement of GnRH Neurons in Mediating the Effects of RFRP-3 on the Mouse Reproductive Axis
title_fullStr SAT-423 The Involvement of GnRH Neurons in Mediating the Effects of RFRP-3 on the Mouse Reproductive Axis
title_full_unstemmed SAT-423 The Involvement of GnRH Neurons in Mediating the Effects of RFRP-3 on the Mouse Reproductive Axis
title_short SAT-423 The Involvement of GnRH Neurons in Mediating the Effects of RFRP-3 on the Mouse Reproductive Axis
title_sort sat-423 the involvement of gnrh neurons in mediating the effects of rfrp-3 on the mouse reproductive axis
topic Neuroendocrinology and Pituitary
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6552017/
http://dx.doi.org/10.1210/js.2019-SAT-423
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