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Social dominance predicts hippocampal glucocorticoid receptor recruitment and resilience to prenatal adversity

The developing fetus is highly sensitive to prenatal stress, which may alter Hypothalamic-Pituitary-Adrenal (HPA) axis programming and increase the risk of behavioral disorders. There is high variability among the human population, wherein many offspring of stressed pregnancies display resilience to...

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Autores principales: Gross, Moshe, Romi, Hava, Miller, Ayala, Pinhasov, Albert
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6018627/
https://www.ncbi.nlm.nih.gov/pubmed/29941995
http://dx.doi.org/10.1038/s41598-018-27988-9
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author Gross, Moshe
Romi, Hava
Miller, Ayala
Pinhasov, Albert
author_facet Gross, Moshe
Romi, Hava
Miller, Ayala
Pinhasov, Albert
author_sort Gross, Moshe
collection PubMed
description The developing fetus is highly sensitive to prenatal stress, which may alter Hypothalamic-Pituitary-Adrenal (HPA) axis programming and increase the risk of behavioral disorders. There is high variability among the human population, wherein many offspring of stressed pregnancies display resilience to adversity, while the remainder displays vulnerability. In order to identify biological substrates mediating between resilience or vulnerability to prenatal adversity, we exposed stress-resistant Dominant (Dom) and stress-sensitive Submissive (Sub) mice to mild prenatal restraint stress (PRS, 45 min on gestational days (GD) 15, 16 and 17). We hypothesized that PRS would differentially alter prenatal programming of limbic regions regulating the HPA axis and affect among Dom and Sub offspring. Indeed, PRS increased Sub offspring’s serum corticosterone, and exaggerated their anxiety- and depressive-like behavior, while Dom offspring remained resilient to the hormonal and behavioral consequences of PRS. Moreover, PRS exposure markedly facilitated glucocorticoid receptor (GR) recruitment to the hippocampus among Dom mice in response to restraint stress, which may be responsible for their resilience to stressful challenge. These findings suggest proclivity to adaptive or maladaptive prenatal programming of hippocampal GR recruitment to be inheritable and predictable by social dominance or submissiveness.
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spelling pubmed-60186272018-07-06 Social dominance predicts hippocampal glucocorticoid receptor recruitment and resilience to prenatal adversity Gross, Moshe Romi, Hava Miller, Ayala Pinhasov, Albert Sci Rep Article The developing fetus is highly sensitive to prenatal stress, which may alter Hypothalamic-Pituitary-Adrenal (HPA) axis programming and increase the risk of behavioral disorders. There is high variability among the human population, wherein many offspring of stressed pregnancies display resilience to adversity, while the remainder displays vulnerability. In order to identify biological substrates mediating between resilience or vulnerability to prenatal adversity, we exposed stress-resistant Dominant (Dom) and stress-sensitive Submissive (Sub) mice to mild prenatal restraint stress (PRS, 45 min on gestational days (GD) 15, 16 and 17). We hypothesized that PRS would differentially alter prenatal programming of limbic regions regulating the HPA axis and affect among Dom and Sub offspring. Indeed, PRS increased Sub offspring’s serum corticosterone, and exaggerated their anxiety- and depressive-like behavior, while Dom offspring remained resilient to the hormonal and behavioral consequences of PRS. Moreover, PRS exposure markedly facilitated glucocorticoid receptor (GR) recruitment to the hippocampus among Dom mice in response to restraint stress, which may be responsible for their resilience to stressful challenge. These findings suggest proclivity to adaptive or maladaptive prenatal programming of hippocampal GR recruitment to be inheritable and predictable by social dominance or submissiveness. Nature Publishing Group UK 2018-06-25 /pmc/articles/PMC6018627/ /pubmed/29941995 http://dx.doi.org/10.1038/s41598-018-27988-9 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Gross, Moshe
Romi, Hava
Miller, Ayala
Pinhasov, Albert
Social dominance predicts hippocampal glucocorticoid receptor recruitment and resilience to prenatal adversity
title Social dominance predicts hippocampal glucocorticoid receptor recruitment and resilience to prenatal adversity
title_full Social dominance predicts hippocampal glucocorticoid receptor recruitment and resilience to prenatal adversity
title_fullStr Social dominance predicts hippocampal glucocorticoid receptor recruitment and resilience to prenatal adversity
title_full_unstemmed Social dominance predicts hippocampal glucocorticoid receptor recruitment and resilience to prenatal adversity
title_short Social dominance predicts hippocampal glucocorticoid receptor recruitment and resilience to prenatal adversity
title_sort social dominance predicts hippocampal glucocorticoid receptor recruitment and resilience to prenatal adversity
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6018627/
https://www.ncbi.nlm.nih.gov/pubmed/29941995
http://dx.doi.org/10.1038/s41598-018-27988-9
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