氧化应激
纳米笼
神经炎症
小胶质细胞
炎症
药理学
医学
重性抑郁障碍
受体
萧条(经济学)
抗氧化剂
补体系统
肽
免疫学
促炎细胞因子
活性氧
氧化磷酸化
病态行为
炎症反应
作者
Meng Shi,Xiangyü Li,Zhen Fan,Yi Wang,Congcong Li,Yuanmeng Ning,Yizhao Ma,Min Sun,Xiaohuan Xia,Jianzhong Du,Jialin Zheng
出处
期刊:ACS Nano
[American Chemical Society]
日期:2025-10-14
卷期号:19 (42): 37186-37205
标识
DOI:10.1021/acsnano.5c11681
摘要
Major depressive disorder (MDD) is the most prevalent neuropsychiatric disorder globally. Promising therapies for MDD are urgently needed due to the limited effectiveness, delayed efficacy, and non-negligible side effects of current treatments. Oxidative stress and neuroinflammation have been recognized as key contributors to MDD. Here, we developed an antioxidant N-acetylcysteine (NAC)-capped Au nanocage (TNNC) that entrapped VGF-derived peptide TLQP21 with neuro-immunomodulatory effects. Once internalized by cells suffering from oxidative stress, NAC was consumed, and TLQP21 was released from TNNC. TNNC administration alleviated MDD-like behaviors of the chronic unpredictable mild stress (CUMS)-exposed mice and effectively relieved oxidative stress in the brains. Moreover, TLQP21 in TNNC inhibits the activation, excessive synaptic pruning, and inflammatory responses of microglia through targeting the complement C1q receptor (C1qR) and complement C3a receptor 1 (C3aR1). This work provides a bioinspired strategy to target multiple pathogenic factors in one nanoparticle for the intervention of MDD and other diseases.
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