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Circadian Control of Neuroendocrine Circuits Regulating Female Reproductive Function

Female reproduction requires the precise temporal organization of interacting, estradiol-sensitive neural circuits that converge to optimally drive hypothalamo-pituitary–gonadal (HPG) axis functioning. In mammals, the master circadian pacemaker in the suprachiasmatic nucleus (SCN) of the anterior hy...

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Autores principales: Williams, Wilbur P., Kriegsfeld, Lance J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Research Foundation 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3356853/
https://www.ncbi.nlm.nih.gov/pubmed/22661968
http://dx.doi.org/10.3389/fendo.2012.00060
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author Williams, Wilbur P.
Kriegsfeld, Lance J.
author_facet Williams, Wilbur P.
Kriegsfeld, Lance J.
author_sort Williams, Wilbur P.
collection PubMed
description Female reproduction requires the precise temporal organization of interacting, estradiol-sensitive neural circuits that converge to optimally drive hypothalamo-pituitary–gonadal (HPG) axis functioning. In mammals, the master circadian pacemaker in the suprachiasmatic nucleus (SCN) of the anterior hypothalamus coordinates reproductively relevant neuroendocrine events necessary to maximize reproductive success. Likewise, in species where periods of fertility are brief, circadian oversight of reproductive function ensures that estradiol-dependent increases in sexual motivation coincide with ovulation. Across species, including humans, disruptions to circadian timing (e.g., through rotating shift work, night shift work, poor sleep hygiene) lead to pronounced deficits in ovulation and fecundity. Despite the well-established roles for the circadian system in female reproductive functioning, the specific neural circuits and neurochemical mediators underlying these interactions are not fully understood. Most work to date has focused on the direct and indirect communication from the SCN to the gonadotropin-releasing hormone (GnRH) system in control of the preovulatory luteinizing hormone (LH) surge. However, the same clock genes underlying circadian rhythms at the cellular level in SCN cells are also common to target cell populations of the SCN, including the GnRH neuronal network. Exploring the means by which the master clock synergizes with subordinate clocks in GnRH cells and its upstream modulatory systems represents an exciting opportunity to further understand the role of endogenous timing systems in female reproduction. Herein we provide an overview of the state of knowledge regarding interactions between the circadian timing system and estradiol-sensitive neural circuits driving GnRH secretion and the preovulatory LH surge.
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spelling pubmed-33568532012-06-01 Circadian Control of Neuroendocrine Circuits Regulating Female Reproductive Function Williams, Wilbur P. Kriegsfeld, Lance J. Front Endocrinol (Lausanne) Endocrinology Female reproduction requires the precise temporal organization of interacting, estradiol-sensitive neural circuits that converge to optimally drive hypothalamo-pituitary–gonadal (HPG) axis functioning. In mammals, the master circadian pacemaker in the suprachiasmatic nucleus (SCN) of the anterior hypothalamus coordinates reproductively relevant neuroendocrine events necessary to maximize reproductive success. Likewise, in species where periods of fertility are brief, circadian oversight of reproductive function ensures that estradiol-dependent increases in sexual motivation coincide with ovulation. Across species, including humans, disruptions to circadian timing (e.g., through rotating shift work, night shift work, poor sleep hygiene) lead to pronounced deficits in ovulation and fecundity. Despite the well-established roles for the circadian system in female reproductive functioning, the specific neural circuits and neurochemical mediators underlying these interactions are not fully understood. Most work to date has focused on the direct and indirect communication from the SCN to the gonadotropin-releasing hormone (GnRH) system in control of the preovulatory luteinizing hormone (LH) surge. However, the same clock genes underlying circadian rhythms at the cellular level in SCN cells are also common to target cell populations of the SCN, including the GnRH neuronal network. Exploring the means by which the master clock synergizes with subordinate clocks in GnRH cells and its upstream modulatory systems represents an exciting opportunity to further understand the role of endogenous timing systems in female reproduction. Herein we provide an overview of the state of knowledge regarding interactions between the circadian timing system and estradiol-sensitive neural circuits driving GnRH secretion and the preovulatory LH surge. Frontiers Research Foundation 2012-05-21 /pmc/articles/PMC3356853/ /pubmed/22661968 http://dx.doi.org/10.3389/fendo.2012.00060 Text en Copyright © 2012 Williamsn III and Kriegsfeld. http://www.frontiersin.org/licenseagreement This is an open-access article distributed under the terms of the Creative Commons Attribution Non Commercial License, which permits non-commercial use, distribution, and reproduction in other forums, provided the original authors and source are credited.
spellingShingle Endocrinology
Williams, Wilbur P.
Kriegsfeld, Lance J.
Circadian Control of Neuroendocrine Circuits Regulating Female Reproductive Function
title Circadian Control of Neuroendocrine Circuits Regulating Female Reproductive Function
title_full Circadian Control of Neuroendocrine Circuits Regulating Female Reproductive Function
title_fullStr Circadian Control of Neuroendocrine Circuits Regulating Female Reproductive Function
title_full_unstemmed Circadian Control of Neuroendocrine Circuits Regulating Female Reproductive Function
title_short Circadian Control of Neuroendocrine Circuits Regulating Female Reproductive Function
title_sort circadian control of neuroendocrine circuits regulating female reproductive function
topic Endocrinology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3356853/
https://www.ncbi.nlm.nih.gov/pubmed/22661968
http://dx.doi.org/10.3389/fendo.2012.00060
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