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A “Timed” Kiss Is Essential for Reproduction: Lessons from Mammalian Studies

Reproduction is associated with the circadian system, primarily as a result of the connectivity between the biological clock in the suprachiasmatic nucleus (SCN) and reproduction-regulating brain regions, such as preoptic area (POA), anteroventral periventricular nucleus (AVPV), and arcuate nucleus...

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Autores principales: Putteeraj, Manish, Soga, Tomoko, Ubuka, Takayoshi, Parhar, Ishwar S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5005330/
https://www.ncbi.nlm.nih.gov/pubmed/27630616
http://dx.doi.org/10.3389/fendo.2016.00121
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author Putteeraj, Manish
Soga, Tomoko
Ubuka, Takayoshi
Parhar, Ishwar S.
author_facet Putteeraj, Manish
Soga, Tomoko
Ubuka, Takayoshi
Parhar, Ishwar S.
author_sort Putteeraj, Manish
collection PubMed
description Reproduction is associated with the circadian system, primarily as a result of the connectivity between the biological clock in the suprachiasmatic nucleus (SCN) and reproduction-regulating brain regions, such as preoptic area (POA), anteroventral periventricular nucleus (AVPV), and arcuate nucleus (ARC). Networking of the central pacemaker to these hypothalamic brain regions is partly represented by close fiber appositions to specialized neurons, such as kisspeptin and gonadotropin-releasing hormone (GnRH) neurons; accounting for rhythmic release of gonadotropins and sex steroids. Numerous studies have attempted to dissect the neurochemical properties of GnRH neurons, which possess intrinsic oscillatory features through the presence of clock genes to regulate the pulsatile and circadian secretion. However, less attention has been given to kisspeptin, the upstream regulator of GnRH and a potent mediator of reproductive functions including puberty. Kisspeptin exerts its stimulatory effects on GnRH secretion via its cognate Kiss-1R receptor that is co-expressed on GnRH neurons. Emerging studies have found that kisspeptin neurons oscillate on a circadian basis and that these neurons also express clock genes that are thought to regulate its rhythmic activities. Based on the fiber networks between the SCN and reproductive nuclei such as the POA, AVPV, and ARC, it is suggested that interactions among the central biological clock and reproductive neurons ensure optimal reproductive functionality. Within this neuronal circuitry, kisspeptin neuronal system is likely to “time” reproduction in a long term during development and aging, in a medium term to regulate circadian or estrus cycle, and in a short term to regulate pulsatile GnRH secretion.
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spelling pubmed-50053302016-09-14 A “Timed” Kiss Is Essential for Reproduction: Lessons from Mammalian Studies Putteeraj, Manish Soga, Tomoko Ubuka, Takayoshi Parhar, Ishwar S. Front Endocrinol (Lausanne) Endocrinology Reproduction is associated with the circadian system, primarily as a result of the connectivity between the biological clock in the suprachiasmatic nucleus (SCN) and reproduction-regulating brain regions, such as preoptic area (POA), anteroventral periventricular nucleus (AVPV), and arcuate nucleus (ARC). Networking of the central pacemaker to these hypothalamic brain regions is partly represented by close fiber appositions to specialized neurons, such as kisspeptin and gonadotropin-releasing hormone (GnRH) neurons; accounting for rhythmic release of gonadotropins and sex steroids. Numerous studies have attempted to dissect the neurochemical properties of GnRH neurons, which possess intrinsic oscillatory features through the presence of clock genes to regulate the pulsatile and circadian secretion. However, less attention has been given to kisspeptin, the upstream regulator of GnRH and a potent mediator of reproductive functions including puberty. Kisspeptin exerts its stimulatory effects on GnRH secretion via its cognate Kiss-1R receptor that is co-expressed on GnRH neurons. Emerging studies have found that kisspeptin neurons oscillate on a circadian basis and that these neurons also express clock genes that are thought to regulate its rhythmic activities. Based on the fiber networks between the SCN and reproductive nuclei such as the POA, AVPV, and ARC, it is suggested that interactions among the central biological clock and reproductive neurons ensure optimal reproductive functionality. Within this neuronal circuitry, kisspeptin neuronal system is likely to “time” reproduction in a long term during development and aging, in a medium term to regulate circadian or estrus cycle, and in a short term to regulate pulsatile GnRH secretion. Frontiers Media S.A. 2016-08-31 /pmc/articles/PMC5005330/ /pubmed/27630616 http://dx.doi.org/10.3389/fendo.2016.00121 Text en Copyright © 2016 Putteeraj, Soga, Ubuka and Parhar. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Endocrinology
Putteeraj, Manish
Soga, Tomoko
Ubuka, Takayoshi
Parhar, Ishwar S.
A “Timed” Kiss Is Essential for Reproduction: Lessons from Mammalian Studies
title A “Timed” Kiss Is Essential for Reproduction: Lessons from Mammalian Studies
title_full A “Timed” Kiss Is Essential for Reproduction: Lessons from Mammalian Studies
title_fullStr A “Timed” Kiss Is Essential for Reproduction: Lessons from Mammalian Studies
title_full_unstemmed A “Timed” Kiss Is Essential for Reproduction: Lessons from Mammalian Studies
title_short A “Timed” Kiss Is Essential for Reproduction: Lessons from Mammalian Studies
title_sort “timed” kiss is essential for reproduction: lessons from mammalian studies
topic Endocrinology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5005330/
https://www.ncbi.nlm.nih.gov/pubmed/27630616
http://dx.doi.org/10.3389/fendo.2016.00121
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