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一种新型抑郁症小鼠模型:在免疫研究和临床转化方面的优势

A Novel Mouse Model of Depression: Advantages in Immune Research and Clinical Translation.

作者信息

Xiong Jing, Zhang Xian-Qiang, Li Ji-Tao, Ren Chi, Shen Tian, Su Yun-Ai, Si Tian-Mei

机构信息

Peking University Sixth Hospital, Peking University Institute of Mental Health, NHC Key Laboratory of Mental Health (Peking University), National Clinical Research Center for Mental Disorders (Peking University Sixth Hospital), China.

Department of Ophthalmology, Eye Disease and Optometry Institute, Peking University People's Hospital, Beijing Key Laboratory of Diagnosis and Therapy of Retinal and Choroid Diseases, China.

出版信息

Int J Biol Sci. 2025 Mar 19;21(6):2446-2461. doi: 10.7150/ijbs.104950. eCollection 2025.

DOI:10.7150/ijbs.104950
PMID:40303307
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12035903/
Abstract

The role of neuroimmune mechanisms in major depressive disorder (MDD) has been gradually highlighted, but existing classical animal models of MDD have limitations in immune inflammation research due to physical injury, high mortality rates, and immune tolerance. This study developed a novel mouse model of depression called the post-witness social defeat stress (PWSDS) model, which combines witness stress with the social defeat paradigm. The model was evaluated based on behavior, central and peripheral immune responses, and predictive validity. The findings revealed that PWSDS-exposed mice exhibited significant anxiety-like behavior, depressive-like behavior, cognitive deficits, and enhanced peripheral and central neuroimmune responses. Additionally, the antidepressant fluoxetine effectively ameliorated the depressive-like phenotypes and immune response in stressed mice. The model captured certain aspects of the behavioral and peripheral immune features of MDD patients. The levels of cortisol and proinflammatory cytokines such as TNFα in the serum of MDD patients with adult stressors increased compared with healthy controls, and were alleviated by SSRIs treatment, accompanied by improvement in depressive symptoms, anxiety symptoms and cognitive impairments. This study establishes an improved mouse model of MDD, which has specific advantages in immune research and offers a novel approach to further study the pathogenesis and new treatment of MDD.

摘要

神经免疫机制在重度抑郁症(MDD)中的作用已逐渐受到关注,但现有的经典MDD动物模型在免疫炎症研究方面存在局限性,原因包括物理损伤、高死亡率和免疫耐受等。本研究开发了一种新型抑郁症小鼠模型,即目睹后社会挫败应激(PWSDS)模型,该模型将目睹应激与社会挫败范式相结合。基于行为、中枢和外周免疫反应以及预测效度对该模型进行了评估。研究结果显示,暴露于PWSDS的小鼠表现出显著的焦虑样行为、抑郁样行为、认知缺陷,以及外周和中枢神经免疫反应增强。此外,抗抑郁药氟西汀有效改善了应激小鼠的抑郁样表型和免疫反应。该模型捕捉到了MDD患者行为和外周免疫特征的某些方面。与健康对照相比,有成年应激源的MDD患者血清中皮质醇和促炎细胞因子(如TNFα)水平升高,经选择性5-羟色胺再摄取抑制剂(SSRI)治疗后得到缓解,同时抑郁症状、焦虑症状和认知障碍也有所改善。本研究建立了一种改良的MDD小鼠模型,该模型在免疫研究方面具有特定优势,为进一步研究MDD的发病机制和新治疗方法提供了一种新途径。

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本文引用的文献

1
The multifaceted effects of fluoxetine treatment on cognitive functions.氟西汀治疗对认知功能的多方面影响。
Front Pharmacol. 2024 Jul 16;15:1412420. doi: 10.3389/fphar.2024.1412420. eCollection 2024.
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Emerging Therapeutic Potential of Fluoxetine on Cognitive Decline in Alzheimer's Disease: Systematic Review.氟西汀对阿尔茨海默病认知衰退的治疗潜力:系统评价。
Int J Mol Sci. 2024 Jun 13;25(12):6542. doi: 10.3390/ijms25126542.
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Down-regulation of MKP-1 in hippocampus protects against stress-induced depression-like behaviors and neuroinflammation.
下调海马中的 MKP-1 可预防应激诱导的抑郁样行为和神经炎症。
Transl Psychiatry. 2024 Mar 1;14(1):130. doi: 10.1038/s41398-024-02846-7.
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Major depressive disorder: hypothesis, mechanism, prevention and treatment.重度抑郁症:假说、机制、预防与治疗。
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Major depressive disorder as a neuro-immune disorder: Origin, mechanisms, and therapeutic opportunities.作为一种神经免疫性疾病的重度抑郁症:起源、机制及治疗机遇
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Proinflammatory phenotype in major depressive disorder with adulthood adversity: In line with social signal transduction theory of depression.成年逆境与重性抑郁障碍中促炎表型:与抑郁的社会信号转导理论一致。
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