Department of Psychiatry, University of California, San Francisco, San Francisco, CA 94143-0848, USA.
Neurosci Biobehav Rev. 2010 Sep;35(1):39-45. doi: 10.1016/j.neubiorev.2010.01.003. Epub 2010 Jan 18.
Major life events involving social rejection are strongly associated with onset of depression. To account for this relation, we propose a psychobiological model in which rejection-related stressors elicit a distinct and integrated set of cognitive, emotional, and biological changes that may evoke depression. In this model, social rejection events activate brain regions involved in processing negative affect and rejection-related distress (e.g., anterior insula, dorsal anterior cingulate cortex). They also elicit negative self-referential cognitions (e.g., "I'm undesirable," "Other people don't like me") and related self-conscious emotions (e.g., shame, humiliation). Downstream biological consequences include upregulation of the hypothalamic-pituitary-adrenal axis, sympathetic-adrenal-medullary axis, and inflammatory response. Pro-inflammatory cytokines play an important role in this process because they induce a constellation of depressotypic behaviors called sickness behaviors. Although these changes can be short-lived, sustained inflammation may occur via glucocorticoid resistance, catecholamines, sympathetic innervation of immune organs, and immune cell aging. This response also may be moderated by several factors, including prior life stress, prior depression, and genes implicated in stress reactivity.
重大的生活事件,涉及社会排斥,与抑郁发作强烈相关。为了解释这种关系,我们提出了一个心理生物学模型,其中与排斥相关的应激源会引起一系列独特而综合的认知、情感和生理变化,这些变化可能会引发抑郁。在这个模型中,社会排斥事件会激活涉及处理负面情绪和与排斥相关的痛苦的大脑区域(例如,前岛叶、背侧前扣带皮层)。它们还会引发消极的自我参照认知(例如,“我不可爱”、“别人不喜欢我”)和相关的自我意识情绪(例如,羞耻、屈辱)。下游的生物学后果包括下丘脑-垂体-肾上腺轴、交感肾上腺髓质轴和炎症反应的上调。促炎细胞因子在这个过程中起着重要的作用,因为它们会引起一系列被称为疾病行为的抑郁样行为。尽管这些变化可能是短暂的,但持续的炎症可能会通过糖皮质激素抵抗、儿茶酚胺、免疫器官的交感神经支配和免疫细胞衰老而发生。这种反应也可能受到多种因素的调节,包括先前的生活压力、先前的抑郁和与应激反应相关的基因。