Chrysin alleviated CUMS-induced depressive-like behaviors in mice via directly targeting Fyn

被引:3
|
作者
Li, Zhipeng [1 ]
Wang, Qingchen [1 ]
Zhang, Zhonghong [1 ]
Guo, Yaping [1 ]
Sun, Mingna [2 ]
Li, Li [3 ]
He, Wenbin [4 ]
机构
[1] Binzhou Med Univ, Sch Pharm, Yantai, Shandong, Peoples R China
[2] Guangzhou Med Univ, Sch Pharmaceut Sci, Guangzhou 511436, Peoples R China
[3] Zhejiang Hosp, Dept Pharm, Hangzhou 310013, Zhejiang, Peoples R China
[4] Shanxi Univ Chinese Med, Shanxi Key Lab Chinese Med Encephalopathy, Taiyuan 030619, Shanxi, Peoples R China
基金
中国国家自然科学基金;
关键词
Chrysin; Neuroinflammation; Fyn; Depression; NF-& kappa; B; KINASE;
D O I
10.1016/j.jff.2023.105603
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
Neuroinflammation is the common pathological feature of neuropsychiatric diseases. Chrysin, a kind of natural flavonoid compound, was reported to exert antidepressant effects, however the direct targets of chrysin remain unclear. Currently studies showed chrysin alleviated CUMS-induced depressive-like behaviors in mice. We found chrysin inhibited CUMS-induced microglia activation in mice. We further found that chrysin inhibited the activation of Fyn and NF-?B pathway, and decreased the expression of iNOS, COX2 and NLRP3. Furthermore, our data showed that chrysin can bind to Fyn using pull-down assay. Transfection siRNA-Fyn abolished the inhibitory effect of chrysin on activation of NF-?B pathway. This study revealed that targeting inhibition of Fyn by chrysin to alleviate CUMS-induced neuroinflammation and depressive-like behaviors via inhibiting the expression of iNOS, COX2 and NLRP3 mediated by inhibition of NF-?B pathway. Thus, this study has revealed, for the first time, Fyn was the direct target of chrysin against neuroinflammation and neuroinflammation-related depression.
引用
收藏
页数:7
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