Birth elicits a conserved neuroendocrine response with implications for perinatal osmoregulation and neuronal cell death

Abstract Long-standing clinical findings report a dramatic surge of vasopressin in umbilical cord blood of the human neonate, but the neural underpinnings and function(s) of this phenomenon remain obscure. We studied neural activation in perinatal mice and rats, and found that birth triggers activat...

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Autores principales: Yarely C. Hoffiz, Alexandra Castillo-Ruiz, Megan A. L. Hall, Taylor A. Hite, Jennifer M. Gray, Carla D. Cisternas, Laura R. Cortes, Andrew J. Jacobs, Nancy G. Forger
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Publicado: Nature Portfolio 2021
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Acceso en línea:https://doaj.org/article/3ffec8c8a6a547f1966ab65d7e48170b
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spelling oai:doaj.org-article:3ffec8c8a6a547f1966ab65d7e48170b2021-12-02T13:57:58ZBirth elicits a conserved neuroendocrine response with implications for perinatal osmoregulation and neuronal cell death10.1038/s41598-021-81511-12045-2322https://doaj.org/article/3ffec8c8a6a547f1966ab65d7e48170b2021-01-01T00:00:00Zhttps://doi.org/10.1038/s41598-021-81511-1https://doaj.org/toc/2045-2322Abstract Long-standing clinical findings report a dramatic surge of vasopressin in umbilical cord blood of the human neonate, but the neural underpinnings and function(s) of this phenomenon remain obscure. We studied neural activation in perinatal mice and rats, and found that birth triggers activation of the suprachiasmatic, supraoptic, and paraventricular nuclei of the hypothalamus. This was seen whether mice were born vaginally or via Cesarean section (C-section), and when birth timing was experimentally manipulated. Neuronal phenotyping showed that the activated neurons were predominantly vasopressinergic, and vasopressin mRNA increased fivefold in the hypothalamus during the 2–3 days before birth. Copeptin, a surrogate marker of vasopressin, was elevated 30-to 50-fold in plasma of perinatal mice, with higher levels after a vaginal than a C-section birth. We also found an acute decrease in plasma osmolality after a vaginal, but not C-section birth, suggesting that the difference in vasopressin release between birth modes is functionally meaningful. When vasopressin was administered centrally to newborns, we found an ~ 50% reduction in neuronal cell death in specific brain areas. Collectively, our results identify a conserved neuroendocrine response to birth that is sensitive to birth mode, and influences peripheral physiology and neurodevelopment.Yarely C. HoffizAlexandra Castillo-RuizMegan A. L. HallTaylor A. HiteJennifer M. GrayCarla D. CisternasLaura R. CortesAndrew J. JacobsNancy G. ForgerNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 11, Iss 1, Pp 1-14 (2021)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Yarely C. Hoffiz
Alexandra Castillo-Ruiz
Megan A. L. Hall
Taylor A. Hite
Jennifer M. Gray
Carla D. Cisternas
Laura R. Cortes
Andrew J. Jacobs
Nancy G. Forger
Birth elicits a conserved neuroendocrine response with implications for perinatal osmoregulation and neuronal cell death
description Abstract Long-standing clinical findings report a dramatic surge of vasopressin in umbilical cord blood of the human neonate, but the neural underpinnings and function(s) of this phenomenon remain obscure. We studied neural activation in perinatal mice and rats, and found that birth triggers activation of the suprachiasmatic, supraoptic, and paraventricular nuclei of the hypothalamus. This was seen whether mice were born vaginally or via Cesarean section (C-section), and when birth timing was experimentally manipulated. Neuronal phenotyping showed that the activated neurons were predominantly vasopressinergic, and vasopressin mRNA increased fivefold in the hypothalamus during the 2–3 days before birth. Copeptin, a surrogate marker of vasopressin, was elevated 30-to 50-fold in plasma of perinatal mice, with higher levels after a vaginal than a C-section birth. We also found an acute decrease in plasma osmolality after a vaginal, but not C-section birth, suggesting that the difference in vasopressin release between birth modes is functionally meaningful. When vasopressin was administered centrally to newborns, we found an ~ 50% reduction in neuronal cell death in specific brain areas. Collectively, our results identify a conserved neuroendocrine response to birth that is sensitive to birth mode, and influences peripheral physiology and neurodevelopment.
format article
author Yarely C. Hoffiz
Alexandra Castillo-Ruiz
Megan A. L. Hall
Taylor A. Hite
Jennifer M. Gray
Carla D. Cisternas
Laura R. Cortes
Andrew J. Jacobs
Nancy G. Forger
author_facet Yarely C. Hoffiz
Alexandra Castillo-Ruiz
Megan A. L. Hall
Taylor A. Hite
Jennifer M. Gray
Carla D. Cisternas
Laura R. Cortes
Andrew J. Jacobs
Nancy G. Forger
author_sort Yarely C. Hoffiz
title Birth elicits a conserved neuroendocrine response with implications for perinatal osmoregulation and neuronal cell death
title_short Birth elicits a conserved neuroendocrine response with implications for perinatal osmoregulation and neuronal cell death
title_full Birth elicits a conserved neuroendocrine response with implications for perinatal osmoregulation and neuronal cell death
title_fullStr Birth elicits a conserved neuroendocrine response with implications for perinatal osmoregulation and neuronal cell death
title_full_unstemmed Birth elicits a conserved neuroendocrine response with implications for perinatal osmoregulation and neuronal cell death
title_sort birth elicits a conserved neuroendocrine response with implications for perinatal osmoregulation and neuronal cell death
publisher Nature Portfolio
publishDate 2021
url https://doaj.org/article/3ffec8c8a6a547f1966ab65d7e48170b
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