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Lack of Ventral Striatal Response to Positive Stimuli in Depressed Versus Normal Subjects

心理学 功能磁共振成像 背景(考古学) 愉快 萧条(经济学) 神经影像学 神经科学 基底神经节 神经功能成像 统计参数映射 腹侧纹状体 意识的神经相关物 磁共振成像 中枢神经系统 纹状体 多巴胺 医学 认知 经济 古生物学 宏观经济学 放射科 生物
作者
Jane Epstein
出处
期刊:American Journal of Psychiatry [American Psychiatric Association]
卷期号:163 (10): 1784-1784 被引量:362
标识
DOI:10.1176/appi.ajp.163.10.1784
摘要

Objective: Most of the functional neuroimaging studies of depression have focused primarily on the resting state or responses to negatively valenced stimuli. However, depression consists not only of an accentuation of negative affective processing but of an inability to experience pleasure or positive motivation. The authors tested the hypothesis that depressed subjects would show less activation than healthy comparison subjects, in response to positive stimuli, in ventral striatal regions associated with processing of reward and positive stimuli. Method: Positive, negative, and neutral words were presented to 10 unmedicated depressed patients and 12 healthy comparison subjects in the context of a 3T functional magnetic resonance imaging (MRI) paradigm. Image processing and analysis were performed using statistical parametric mapping with a mixed-effects model. Significant differences in neural responses were assessed, examining group, condition, and interaction effects of interest within the context of a general linear model. Results: Relative to comparison subjects, depressed patients demonstrated significantly less bilateral ventral striatal activation to positive stimuli, correlating with decreased interest/pleasure in and performance of activities. They also displayed decreased activation to positive stimuli in a dorsomedial frontal region associated with processing of self-related stimuli. Responses of depressed subjects to negative stimuli were consistent with the growing literature on frontolimbic dysfunction in depression. Conclusions: This finding 1) supports a pathophysiological model of depression that includes reward/motivational pathway dysfunction, 2) suggests a contributing neural substrate of the inability to experience pleasure or engage in rewarding activities, 3) provides greater specification of abnormalities of basal ganglia function in depression, and 4) may help guide treatment approaches.

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