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Relaxin-3 stimulates the hypothalamic-pituitary-gonadal axis
The hypothalamus plays a key role in the regulation of both energy homeostasis and reproduction. Evidence suggests that relaxin-3, a recently discovered member of the insulin superfamily, is an orexigenic hypothalamic neuropeptide. Relaxin-3 is thought to act in the brain via the RXFP3 receptor, alt...
Autores principales: | , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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American Physiological Society
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2519759/ https://www.ncbi.nlm.nih.gov/pubmed/18492777 http://dx.doi.org/10.1152/ajpendo.00028.2008 |
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author | McGowan, B. M. Stanley, S. A. Donovan, J. Thompson, E. L. Patterson, M. Semjonous, N. M. Gardiner, J. V. Murphy, K. G. Ghatei, M. A. Bloom, S. R. |
author_facet | McGowan, B. M. Stanley, S. A. Donovan, J. Thompson, E. L. Patterson, M. Semjonous, N. M. Gardiner, J. V. Murphy, K. G. Ghatei, M. A. Bloom, S. R. |
author_sort | McGowan, B. M. |
collection | PubMed |
description | The hypothalamus plays a key role in the regulation of both energy homeostasis and reproduction. Evidence suggests that relaxin-3, a recently discovered member of the insulin superfamily, is an orexigenic hypothalamic neuropeptide. Relaxin-3 is thought to act in the brain via the RXFP3 receptor, although the RXFP1 receptor may also play a role. Relaxin-3, RXFP3, and RXFP1 are present in the hypothalamic paraventricular nucleus, an area with a well-characterized role in the regulation of energy balance that also modulates reproductive function by providing inputs to hypothalamic gonadotropin-releasing hormone (GnRH) neurons. Other members of the relaxin family are known to play a role in the regulation of reproduction. However, the effects of relaxin-3 on reproductive function are unknown. We studied the role of relaxin-3 in the regulation of the hypothalamo-pituitary-gonadal (HPG) axis. Intracerebroventricular (5 nmol) and intraparaventricular (540–1,620 pmol) administration of human relaxin-3 (H3) in adult male Wistar rats significantly increased plasma luteinizing hormone (LH) 30 min postinjection. This effect was blocked by pretreatment with a peripheral GnRH antagonist. Central administration of human relaxin-2 showed no significant effect on plasma LH. H3 dose-dependently stimulated the release of GnRH from hypothalamic explants and GT(1)-7 cells, which express RXFP1 and RXFP3, but did not influence LH or follicle-stimulating hormone release from pituitary fragments in vitro. We have demonstrated a novel role for relaxin-3 in the stimulation of the HPG axis, putatively via hypothalamic GnRH neurons. Relaxin-3 may act as a central signal linking nutritional status and reproductive function. |
format | Text |
id | pubmed-2519759 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | American Physiological Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-25197592009-08-01 Relaxin-3 stimulates the hypothalamic-pituitary-gonadal axis McGowan, B. M. Stanley, S. A. Donovan, J. Thompson, E. L. Patterson, M. Semjonous, N. M. Gardiner, J. V. Murphy, K. G. Ghatei, M. A. Bloom, S. R. Am J Physiol Endocrinol Metab Articles The hypothalamus plays a key role in the regulation of both energy homeostasis and reproduction. Evidence suggests that relaxin-3, a recently discovered member of the insulin superfamily, is an orexigenic hypothalamic neuropeptide. Relaxin-3 is thought to act in the brain via the RXFP3 receptor, although the RXFP1 receptor may also play a role. Relaxin-3, RXFP3, and RXFP1 are present in the hypothalamic paraventricular nucleus, an area with a well-characterized role in the regulation of energy balance that also modulates reproductive function by providing inputs to hypothalamic gonadotropin-releasing hormone (GnRH) neurons. Other members of the relaxin family are known to play a role in the regulation of reproduction. However, the effects of relaxin-3 on reproductive function are unknown. We studied the role of relaxin-3 in the regulation of the hypothalamo-pituitary-gonadal (HPG) axis. Intracerebroventricular (5 nmol) and intraparaventricular (540–1,620 pmol) administration of human relaxin-3 (H3) in adult male Wistar rats significantly increased plasma luteinizing hormone (LH) 30 min postinjection. This effect was blocked by pretreatment with a peripheral GnRH antagonist. Central administration of human relaxin-2 showed no significant effect on plasma LH. H3 dose-dependently stimulated the release of GnRH from hypothalamic explants and GT(1)-7 cells, which express RXFP1 and RXFP3, but did not influence LH or follicle-stimulating hormone release from pituitary fragments in vitro. We have demonstrated a novel role for relaxin-3 in the stimulation of the HPG axis, putatively via hypothalamic GnRH neurons. Relaxin-3 may act as a central signal linking nutritional status and reproductive function. American Physiological Society 2008-08 2008-05-20 /pmc/articles/PMC2519759/ /pubmed/18492777 http://dx.doi.org/10.1152/ajpendo.00028.2008 Text en Copyright © 2008, American Physiological Society This document may be redistributed and reused, subject to www.the-aps.org/publications/journals/funding_addendum_policy.htm (http://www.the-aps.org/publications/journals/funding_addendum_policy.htm) . |
spellingShingle | Articles McGowan, B. M. Stanley, S. A. Donovan, J. Thompson, E. L. Patterson, M. Semjonous, N. M. Gardiner, J. V. Murphy, K. G. Ghatei, M. A. Bloom, S. R. Relaxin-3 stimulates the hypothalamic-pituitary-gonadal axis |
title | Relaxin-3 stimulates the hypothalamic-pituitary-gonadal axis |
title_full | Relaxin-3 stimulates the hypothalamic-pituitary-gonadal axis |
title_fullStr | Relaxin-3 stimulates the hypothalamic-pituitary-gonadal axis |
title_full_unstemmed | Relaxin-3 stimulates the hypothalamic-pituitary-gonadal axis |
title_short | Relaxin-3 stimulates the hypothalamic-pituitary-gonadal axis |
title_sort | relaxin-3 stimulates the hypothalamic-pituitary-gonadal axis |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2519759/ https://www.ncbi.nlm.nih.gov/pubmed/18492777 http://dx.doi.org/10.1152/ajpendo.00028.2008 |
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