Neuro-Epigenetics Research Group, School of Clinical Sciences, University of Bristol, Dorothy Hodgkin Building, Whitson Street, Bristol BS1 3NY, United Kingdom.
Neurobiology of Stress and Behaviour Research Group, School of Clinical Sciences, University of Bristol, Dorothy Hodgkin Building, Whitson Street, Bristol BS1 3NY, United Kingdom.
Neurobiol Stress. 2014 Oct 15;1:44-59. doi: 10.1016/j.ynstr.2014.10.001. eCollection 2015 Jan.
Glucocorticoid hormones play a pivotal role in the response to stressful challenges. The surge in glucocorticoid hormone secretion after stress needs to be tightly controlled with characteristics like peak height, curvature and duration depending on the nature and severity of the challenge. This is important as chronic hyper- or hypo-responses are detrimental to health due to increasing the risk for developing a stress-related mental disorder. Proper glucocorticoid responses to stress are critical for adaptation. Therefore, the tight control of baseline and stress-evoked glucocorticoid secretion are important constituents of an organism's resilience. Here, we address a number of mechanisms that illustrate the multitude and complexity of measures safeguarding the control of glucocorticoid function. These mechanisms include the control of mineralocorticoid (MR) and glucocorticoid receptor (GR) occupancy and concentration, the dynamic control of free glucocorticoid hormone availability by corticosteroid-binding globulin (CBG), and the control exerted by glucocorticoids at the signaling, epigenetic and genomic level on gene transcriptional responses to stress. We review the beneficial effects of regular exercise on HPA axis and sleep physiology, and cognitive and anxiety-related behavior. Furthermore, we describe that, possibly through changes in the GABAergic system, exercise reduces the impact of stress on a signaling pathway specifically in the dentate gyrus that is strongly implicated in the behavioral response to that stressor. These observations underline the impact of life style on stress resilience. Finally, we address how single nucleotide polymorphisms (SNPs) affecting glucocorticoid action can compromise stress resilience, which becomes most apparent under conditions of childhood abuse.
糖皮质激素在应对应激挑战中起着关键作用。应激后糖皮质激素分泌的激增需要根据挑战的性质和严重程度,通过峰值高度、曲率和持续时间等特征进行严格控制。这很重要,因为慢性高反应或低反应会因增加患与压力相关的精神障碍的风险而对健康造成损害。适当的糖皮质激素对应激的反应对于适应至关重要。因此,基础和应激诱导的糖皮质激素分泌的严格控制是生物体弹性的重要组成部分。在这里,我们介绍了许多机制,这些机制说明了多种措施对于保障糖皮质激素功能控制的复杂性。这些机制包括盐皮质激素(MR)和糖皮质激素受体(GR)占据和浓度的控制、糖皮质激素结合球蛋白(CBG)对游离糖皮质激素可用性的动态控制,以及糖皮质激素在信号转导、表观遗传和基因组水平上对基因转录对应激的反应的控制。我们回顾了有规律的运动对 HPA 轴和睡眠生理学以及认知和焦虑相关行为的有益影响。此外,我们描述了运动可能通过改变 GABA 能系统,减少应激对齿状回信号通路的影响,而齿状回在对该应激源的行为反应中起着重要作用。这些观察结果强调了生活方式对压力弹性的影响。最后,我们讨论了影响糖皮质激素作用的单核苷酸多态性(SNPs)如何影响压力弹性,在儿童虐待的情况下,这种影响最为明显。
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