Furuyashiki Tomoyuki, Deguchi Yuichi
Department of Pharmacology, Kyoto University Graduate School of Medicine, Kyoto, Japan.
Brain Nerve. 2012 Aug;64(8):919-26.
Major depression, a psychiatric disorder characterized by depressive mood and loss of interest and pleasure, is a leading cause of disability and suicide in developed countries. However, the mechanisms that underlie major depression remain to be elucidated. Clinical studies on patients with major depression have shown abnormalities in multiple brain areas, each of which can account for a distinct symptom or endophenotype. Notably, the striatum in healthy control subjects responds to positive emotional stimuli and to positive feedback signals during cognitive tasks, but these striatal responses are greatly reduced in depressive patients. Given the role of the striatum in behavioral learning with positive reinforcers, abnormalities as such suggest that impairment in reward processing and/or reinforcement learning in major depression is the basis of anhedonia and reduced psychomotor activity. In animal studies, stress -a risk factor for major depression- is frequently used to induce behavioral depression. Repeated social defeat stress increases the excitability of dopamine neurons and subsequent CREB-mediated transcription in the nucleus accumbens shell, leading to behavioral depression. Surprisingly, this pathway seems not to be involved in behavioral depression caused by prolonged social isolation, suggesting distinct mechanisms underlying the two stressful contexts. In contrast, ΔFosB-mediated gene expression in the nucleus accumbens shell confers resilience to stress. Repeated social defeat stress induces accumbal ΔFosB expression in a stress-resilient subset of individuals, whereas prolonged social isolation decreases this expression, leading to stress susceptibility. In addition to emotional changes, chronic stress also alters the mode of instrumental behavior from goal-directed to habitual responding, with consistent morphological changes in striatal subregions responsible for the corresponding behavioral modes. Therefore, these clinical and preclinical findings suggest that striatal abnormalities play a role in emotional and cognitive changes associated with major depression.
重度抑郁症是一种以情绪低落、兴趣和愉悦感丧失为特征的精神障碍,是发达国家残疾和自杀的主要原因。然而,重度抑郁症的潜在机制仍有待阐明。对重度抑郁症患者的临床研究表明,多个脑区存在异常,每个脑区都可解释一种独特的症状或内表型。值得注意的是,健康对照受试者的纹状体在认知任务期间对积极情绪刺激和积极反馈信号有反应,但抑郁症患者的这些纹状体反应大大降低。鉴于纹状体在通过积极强化物进行行为学习中的作用,此类异常表明,重度抑郁症中奖励处理和/或强化学习受损是快感缺失和精神运动活动减少的基础。在动物研究中,压力(重度抑郁症的一个风险因素)常被用于诱发行为性抑郁。反复的社会挫败应激会增加多巴胺能神经元的兴奋性以及伏隔核壳中随后的CREB介导的转录,从而导致行为性抑郁。令人惊讶的是,这条通路似乎不参与由长期社会隔离引起的行为性抑郁,这表明两种应激情境背后存在不同的机制。相比之下,伏隔核壳中ΔFosB介导的基因表达赋予对应激的恢复力。反复的社会挫败应激会在一部分具有应激恢复力的个体中诱导伏隔核ΔFosB表达,而长期社会隔离会降低这种表达,导致对应激敏感。除了情绪变化外,慢性应激还会将工具性的行为模式从目标导向转变为习惯性反应,负责相应行为模式的纹状体亚区会出现一致的形态学变化。因此,这些临床和临床前研究结果表明,纹状体异常在与重度抑郁症相关的情绪和认知变化中起作用。