Early-life stress, HPA axis adaptation, and mechanisms contributing to later health outcomes

被引:203
|
作者
Maniam, Jayanthi [1 ]
Antoniadis, Christopher [1 ]
Morris, Margaret J. [1 ]
机构
[1] UNSW Australia, Sch Med Sci, Dept Pharmacol, Sydney, NSW 2052, Australia
来源
关键词
early-life stress; metabolic disorders; 11-beta hydroxysteroid dehydrogenase 1; hyperinsulinemia; liver; insulin signaling; glucocorticoids;
D O I
10.3389/fendo.2014.00073
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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 (11 beta-HSD1). We propose that interactions between altered HPA axis activity and liver 11 beta-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.
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页数:17
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