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Molecular and Environmental Mechanisms Regulating Puberty Initiation: An Integrated Approach

The mechanisms underlying the initiation of puberty, one of the cornerstones of human evolution, have not been fully elucidated as yet. However, recently, an accumulating body of evidence has helped unravel several critical aspects of the process. It is clear that a change in the pattern of pituitar...

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Autores principales: Livadas, Sarantis, Chrousos, George P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6915095/
https://www.ncbi.nlm.nih.gov/pubmed/31920956
http://dx.doi.org/10.3389/fendo.2019.00828
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author Livadas, Sarantis
Chrousos, George P.
author_facet Livadas, Sarantis
Chrousos, George P.
author_sort Livadas, Sarantis
collection PubMed
description The mechanisms underlying the initiation of puberty, one of the cornerstones of human evolution, have not been fully elucidated as yet. However, recently, an accumulating body of evidence has helped unravel several critical aspects of the process. It is clear that a change in the pattern of pituitary gonadotropin secretion serves as a hormonal trigger for puberty induction. This change is directly guided by the hypothalamic GnRH pulse generation, a phenomenon regulated by the Kisspeptin-Neurokinin-Dynorphin (KNDy) system also in the hypothalamus. This represents the kisspeptin molecule, which is crucial in augmenting GnRH secretion at puberty, whose secretion is fine-tuned by the opposing signals neurokinin B and dynorphin. Recently, the novel kisspeptin inhibitory signal MKRN3 was described, whose role in puberty initiation provided further insight into the mechanistic aspects of pubertal onset. Furthermore, the description of higher inhibitory and stimulatory signals acting upstream of the KNDy neurons suggested that the trigger point of puberty is located upstream of the KNDy system and the GnRH pulse generator. However, the mechanism of pubertal onset should not be considered as an isolated closed loop system. On the contrary, it is influenced by such factors as adipose tissue, gastrointestinal function, adrenal androgen production, energy sensing, and physical and psychosocial stress. Also, fetal and early life stressful events, as well as exposure to endocrine disruptors, may play important roles in pubertal initiation, the latter primarily through epigenetic modifications. Here we present the available data in the field and attempt to provide an integrated view of this unique and crucial phenomenon.
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spelling pubmed-69150952020-01-09 Molecular and Environmental Mechanisms Regulating Puberty Initiation: An Integrated Approach Livadas, Sarantis Chrousos, George P. Front Endocrinol (Lausanne) Endocrinology The mechanisms underlying the initiation of puberty, one of the cornerstones of human evolution, have not been fully elucidated as yet. However, recently, an accumulating body of evidence has helped unravel several critical aspects of the process. It is clear that a change in the pattern of pituitary gonadotropin secretion serves as a hormonal trigger for puberty induction. This change is directly guided by the hypothalamic GnRH pulse generation, a phenomenon regulated by the Kisspeptin-Neurokinin-Dynorphin (KNDy) system also in the hypothalamus. This represents the kisspeptin molecule, which is crucial in augmenting GnRH secretion at puberty, whose secretion is fine-tuned by the opposing signals neurokinin B and dynorphin. Recently, the novel kisspeptin inhibitory signal MKRN3 was described, whose role in puberty initiation provided further insight into the mechanistic aspects of pubertal onset. Furthermore, the description of higher inhibitory and stimulatory signals acting upstream of the KNDy neurons suggested that the trigger point of puberty is located upstream of the KNDy system and the GnRH pulse generator. However, the mechanism of pubertal onset should not be considered as an isolated closed loop system. On the contrary, it is influenced by such factors as adipose tissue, gastrointestinal function, adrenal androgen production, energy sensing, and physical and psychosocial stress. Also, fetal and early life stressful events, as well as exposure to endocrine disruptors, may play important roles in pubertal initiation, the latter primarily through epigenetic modifications. Here we present the available data in the field and attempt to provide an integrated view of this unique and crucial phenomenon. Frontiers Media S.A. 2019-12-06 /pmc/articles/PMC6915095/ /pubmed/31920956 http://dx.doi.org/10.3389/fendo.2019.00828 Text en Copyright © 2019 Livadas and Chrousos. 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) and the copyright owner(s) 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
Livadas, Sarantis
Chrousos, George P.
Molecular and Environmental Mechanisms Regulating Puberty Initiation: An Integrated Approach
title Molecular and Environmental Mechanisms Regulating Puberty Initiation: An Integrated Approach
title_full Molecular and Environmental Mechanisms Regulating Puberty Initiation: An Integrated Approach
title_fullStr Molecular and Environmental Mechanisms Regulating Puberty Initiation: An Integrated Approach
title_full_unstemmed Molecular and Environmental Mechanisms Regulating Puberty Initiation: An Integrated Approach
title_short Molecular and Environmental Mechanisms Regulating Puberty Initiation: An Integrated Approach
title_sort molecular and environmental mechanisms regulating puberty initiation: an integrated approach
topic Endocrinology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6915095/
https://www.ncbi.nlm.nih.gov/pubmed/31920956
http://dx.doi.org/10.3389/fendo.2019.00828
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