Chronic social defeat stress impairs goal-directed behavior through dysregulation of ventral hippocampal activity in male mice

社会失败 心理学 神经科学 抗抑郁药 5-羟色胺再摄取抑制剂 海马结构 光遗传学 社会压力 抑郁症动物模型 西酞普兰 行为激活 行为绝望测验 海马体 认知
作者
Keitaro Yoshida,Michael R. Drew,Anna Kono,Masaru Mimura,Norio Takata,Kenji F. Tanaka
出处
期刊:Neuropsychopharmacology [Springer Nature]
卷期号:46 (9): 1606-1616 被引量:38
标识
DOI:10.1038/s41386-021-00990-y
摘要

Abstract Chronic stress is a risk factor for a variety of psychiatric disorders, including depression. Although impairments to motivated behavior are a major symptom of clinical depression, little is known about the circuit mechanisms through which stress impairs motivation. Furthermore, research in animal models for depression has focused on impairments to hedonic aspects of motivation, whereas patient studies suggest that impairments to appetitive, goal-directed motivation contribute significantly to motivational impairments in depression. Here, we characterized goal-directed motivation in repeated social defeat stress (R-SDS), a well-established mouse model for depression in male mice. R-SDS impaired the ability to sustain and complete goal-directed behavior in a food-seeking operant lever-press task. Furthermore, stress-exposed mice segregated into susceptible and resilient subpopulations. Interestingly, susceptibility to stress-induced motivational impairments was unrelated to stress-induced social withdrawal, another prominent effect of R-SDS in mouse models. Based on evidence that ventral hippocampus (vHP) modulates sustainment of goal-directed behavior, we monitored vHP activity during the task using fiber photometry. Successful task completion was associated with suppression of ventral hippocampal neural activity. This suppression was diminished after R-SDS in stress-susceptible but not stress-resilient mice. The serotonin selective reuptake inhibitor (SSRI) escitalopram and ketamine both normalized vHP activity during the task and restored motivated behavior. Furthermore, optogenetic vHP inhibition was sufficient to restore motivated behavior after stress. These results identify vHP hyperactivity as a circuit mechanism of stress-induced impairments to goal-directed behavior and a putative biomarker that is sensitive to antidepressant treatments and that differentiates susceptible and resilient individuals.
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