Hall Baila S, Moda Rachel N, Liston Conor
Brain and Mind Research Institute and Program in Neuroscience, Weill Cornell Medical College, 413 East 69 Street, Box 240, New York, NY 10021.
Brain and Mind Research Institute and Program in Neuroscience, Weill Cornell Medical College, 413 East 69 Street, Box 240, New York, NY 10021 ; Sackler Institute for Developmental Psychobiology, Weill Cornell Medical College, 413 East 69 Street, Box 240, New York, NY 10021 ; Department of Psychiatry, Weill Cornell Medical College, 413 East 69 Street, Box 240, New York, NY 10021.
Neurobiol Stress. 2015 Jan 1;1:174-183. doi: 10.1016/j.ynstr.2014.10.008.
Stress-especially chronic, uncontrollable stress-is an important risk factor for many neuropsychiatric disorders. The underlying mechanisms are complex and multifactorial, but they involve correlated changes in structural and functional measures of neuronal connectivity within cortical microcircuits and across neuroanatomically distributed brain networks. Here, we review evidence from animal models and human neuroimaging studies implicating stress-associated changes in functional connectivity in the pathogenesis of PTSD, depression, and other neuropsychiatric conditions. Changes in fMRI measures of corticocortical connectivity across distributed networks may be caused by specific structural alterations that have been observed in the prefrontal cortex, hippocampus, and other vulnerable brain regions. These effects are mediated in part by glucocorticoids, which are released from the adrenal gland in response to a stressor and also oscillate in synchrony with diurnal rhythms. Recent work indicates that circadian glucocorticoid oscillations act to balance synapse formation and pruning after learning and during development, and chronic stress disrupts this balance. We conclude by considering how disrupted glucocorticoid oscillations may contribute to the pathophysiology of depression and PTSD in vulnerable individuals, and how circadian rhythm disturbances may affect non-psychiatric populations, including frequent travelers, shift workers, and patients undergoing treatment for autoimmune disorders.
压力——尤其是慢性的、无法控制的压力——是许多神经精神疾病的重要风险因素。其潜在机制复杂且多因素,但涉及皮质微回路内以及神经解剖学上分布的脑网络之间神经元连接的结构和功能测量的相关变化。在此,我们综述了来自动物模型和人类神经影像学研究的证据,这些证据表明功能连接的压力相关变化在创伤后应激障碍、抑郁症和其他神经精神疾病的发病机制中起作用。跨分布式网络的皮质皮质连接的功能磁共振成像测量变化可能由前额叶皮质、海马体和其他易损脑区中观察到的特定结构改变引起。这些效应部分由糖皮质激素介导,糖皮质激素在应激源作用下从肾上腺释放,并且也与昼夜节律同步振荡。最近的研究表明,昼夜糖皮质激素振荡在学习后和发育过程中起到平衡突触形成和修剪的作用,而慢性压力会破坏这种平衡。我们通过考虑糖皮质激素振荡紊乱如何可能导致易感个体的抑郁症和创伤后应激障碍的病理生理学,以及昼夜节律紊乱如何可能影响非精神疾病人群,包括频繁旅行者、轮班工作者和接受自身免疫性疾病治疗的患者,来得出结论。