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慢性社会挫败应激通过调节雄性小鼠腹侧海马体活动损害了其目标导向行为。

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

机构信息

Department of Neuropsychiatry, Keio University School of Medicine, Tokyo, Japan.

Center for Learning and Memory, Department of Neuroscience, The University of Texas at Austin, Austin, TX, USA.

出版信息

Neuropsychopharmacology. 2021 Aug;46(9):1606-1616. doi: 10.1038/s41386-021-00990-y. Epub 2021 Mar 10.

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.

摘要

慢性应激是多种精神疾病的风险因素,包括抑郁症。尽管动机行为受损是临床抑郁症的主要症状之一,但对于应激如何损害动机的回路机制知之甚少。此外,抑郁症动物模型的研究集中在对动机愉悦方面的损害,而患者研究表明,对食欲、目标导向动机的损害对抑郁症中的动机损害有重要贡献。在这里,我们在雄性小鼠中描述了重复社会挫败应激(R-SDS)的目标导向动机,R-SDS 是一种用于抑郁症的成熟小鼠模型。R-SDS 损害了在食物寻求操作性杠杆按压任务中维持和完成目标导向行为的能力。此外,应激暴露的小鼠分为易感和弹性亚群。有趣的是,对压力引起的动机障碍的易感性与压力引起的社交回避无关,这是 R-SDS 在小鼠模型中的另一个突出效应。基于腹侧海马(vHP)调节目标导向行为的维持的证据,我们使用光纤光度法在任务期间监测 vHP 活动。成功完成任务与抑制腹侧海马神经活动有关。这种抑制在应激易感但应激弹性小鼠中 R-SDS 后减弱。选择性 5-羟色胺再摄取抑制剂(SSRI)依他普仑和氯胺酮都能使任务期间的 vHP 活动正常化,并恢复动机行为。此外,光遗传 vHP 抑制足以在应激后恢复动机行为。这些结果将 vHP 过度活跃确定为应激引起的目标导向行为障碍的回路机制,以及一种潜在的生物标志物,对抗抑郁治疗敏感,并区分易感和弹性个体。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aad2/8280175/3f596b696d5c/41386_2021_990_Fig1_HTML.jpg

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