Shumake J, Gonzalez-Lima F
Department of Psycology, University of Texas at Austin, USA.
Behav Cogn Neurosci Rev. 2003 Sep;2(3):198-221. doi: 10.1177/1534582303259057.
There has been a relative lack of research into the neurobiological predispositions that confer vulnerability to depression. This article reviews functional brain mappings from a genetic animal model, the congenitally helpless rat, which is predisposed to develop learned helplessness. Neurometabolic findings from this model are integrated with the neuroscientific literature from other animal models of depression as well as depressed humans. Changes in four major brain systems are suggested to underlie susceptibility to helplessness and possibly depression: (a) an unbalanced prefrontal-cingulate cortical system, (b) a dissociated hypothalamic-pituitary-adrenal axis, (c) a dissociated septal-hippocampal system, and (d) a hypoactive brain reward system, as exemplified by a hypermetabolic habenula-interpeduncular nucleus pathway and a hypometabolic ventral tegmental area-striatum pathway. Functional interconnections and causal relationships among these systems are considered and further experiments are suggested, with theoretical attention to how an abnormality in any one system could affect the others.
对于那些使人易患抑郁症的神经生物学易感性,相关研究相对较少。本文回顾了来自一种遗传动物模型——先天性无助大鼠的功能性脑图谱,这种大鼠易发展出习得性无助。该模型的神经代谢研究结果与来自其他抑郁症动物模型以及抑郁症患者的神经科学文献相结合。研究表明,四个主要脑系统的变化是易患无助感乃至可能患抑郁症的基础:(a)前额叶 - 扣带回皮质系统失衡;(b)下丘脑 - 垂体 - 肾上腺轴解离;(c)隔区 - 海马系统解离;(d)脑奖赏系统活性不足,例如缰核 - 脚间核通路代谢亢进和腹侧被盖区 - 纹状体通路代谢减退。文中考虑了这些系统之间的功能联系和因果关系,并提出了进一步的实验建议,从理论上关注任何一个系统的异常如何影响其他系统。