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Early-Life Stress, HPA Axis Adaptation, and Mechanisms Contributing to Later Health Outcomes
Stress activates the hypothalamic–pituitary–adrenal (HPA) axis, which then modulates the degree of adaptation and response to a later stressor. It is known that early-life stress can impact on later health but less is known about how early-life stress impairs HPA axis activity, contributing to malad...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2014
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4026717/ https://www.ncbi.nlm.nih.gov/pubmed/24860550 http://dx.doi.org/10.3389/fendo.2014.00073 |
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author | Maniam, Jayanthi Antoniadis, Christopher Morris, Margaret J. |
author_facet | Maniam, Jayanthi Antoniadis, Christopher Morris, Margaret J. |
author_sort | Maniam, Jayanthi |
collection | PubMed |
description | Stress activates the hypothalamic–pituitary–adrenal (HPA) axis, which then modulates the degree of adaptation and response to a later stressor. It is known that early-life stress can impact on later health but less is known about how early-life stress impairs HPA axis activity, contributing to maladaptation of the stress–response system. Early-life stress exposure (either prenatally or in the early postnatal period) can impact developmental pathways resulting in lasting structural and regulatory changes that predispose to adulthood disease. Epidemiological, clinical, and experimental studies have demonstrated that early-life stress produces long term hyper-responsiveness to stress with exaggerated circulating glucocorticoids, and enhanced anxiety and depression-like behaviors. Recently, evidence has emerged on early-life stress-induced metabolic derangements, for example hyperinsulinemia and altered insulin sensitivity on exposure to a high energy diet later in life. This draws our attention to the contribution of later environment to disease vulnerability. Early-life stress can alter the expression of genes in peripheral tissues, such as the glucocorticoid receptor and 11-beta hydroxysteroid dehydrogenase (11β-HSD1). We propose that interactions between altered HPA axis activity and liver 11β-HSD1 modulates both tissue and circulating glucocorticoid availability, with adverse metabolic consequences. This review discusses the potential mechanisms underlying early-life stress-induced maladaptation of the HPA axis, and its subsequent effects on energy utilization and expenditure. The effects of positive later environments as a means of ameliorating early-life stress-induced health deficits, and proposed mechanisms underpinning the interaction between early-life stress and subsequent detrimental environmental exposures on metabolic risk will be outlined. Limitations in current methodology linking early-life stress and later health outcomes will also be addressed. |
format | Online Article Text |
id | pubmed-4026717 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-40267172014-05-23 Early-Life Stress, HPA Axis Adaptation, and Mechanisms Contributing to Later Health Outcomes Maniam, Jayanthi Antoniadis, Christopher Morris, Margaret J. Front Endocrinol (Lausanne) Endocrinology Stress activates the hypothalamic–pituitary–adrenal (HPA) axis, which then modulates the degree of adaptation and response to a later stressor. It is known that early-life stress can impact on later health but less is known about how early-life stress impairs HPA axis activity, contributing to maladaptation of the stress–response system. Early-life stress exposure (either prenatally or in the early postnatal period) can impact developmental pathways resulting in lasting structural and regulatory changes that predispose to adulthood disease. Epidemiological, clinical, and experimental studies have demonstrated that early-life stress produces long term hyper-responsiveness to stress with exaggerated circulating glucocorticoids, and enhanced anxiety and depression-like behaviors. Recently, evidence has emerged on early-life stress-induced metabolic derangements, for example hyperinsulinemia and altered insulin sensitivity on exposure to a high energy diet later in life. This draws our attention to the contribution of later environment to disease vulnerability. Early-life stress can alter the expression of genes in peripheral tissues, such as the glucocorticoid receptor and 11-beta hydroxysteroid dehydrogenase (11β-HSD1). We propose that interactions between altered HPA axis activity and liver 11β-HSD1 modulates both tissue and circulating glucocorticoid availability, with adverse metabolic consequences. This review discusses the potential mechanisms underlying early-life stress-induced maladaptation of the HPA axis, and its subsequent effects on energy utilization and expenditure. The effects of positive later environments as a means of ameliorating early-life stress-induced health deficits, and proposed mechanisms underpinning the interaction between early-life stress and subsequent detrimental environmental exposures on metabolic risk will be outlined. Limitations in current methodology linking early-life stress and later health outcomes will also be addressed. Frontiers Media S.A. 2014-05-13 /pmc/articles/PMC4026717/ /pubmed/24860550 http://dx.doi.org/10.3389/fendo.2014.00073 Text en Copyright © 2014 Maniam, Antoniadis and Morris. http://creativecommons.org/licenses/by/3.0/ 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 Maniam, Jayanthi Antoniadis, Christopher Morris, Margaret J. Early-Life Stress, HPA Axis Adaptation, and Mechanisms Contributing to Later Health Outcomes |
title | Early-Life Stress, HPA Axis Adaptation, and Mechanisms Contributing to Later Health Outcomes |
title_full | Early-Life Stress, HPA Axis Adaptation, and Mechanisms Contributing to Later Health Outcomes |
title_fullStr | Early-Life Stress, HPA Axis Adaptation, and Mechanisms Contributing to Later Health Outcomes |
title_full_unstemmed | Early-Life Stress, HPA Axis Adaptation, and Mechanisms Contributing to Later Health Outcomes |
title_short | Early-Life Stress, HPA Axis Adaptation, and Mechanisms Contributing to Later Health Outcomes |
title_sort | early-life stress, hpa axis adaptation, and mechanisms contributing to later health outcomes |
topic | Endocrinology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4026717/ https://www.ncbi.nlm.nih.gov/pubmed/24860550 http://dx.doi.org/10.3389/fendo.2014.00073 |
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