Resveratrol ameliorates lipopolysaccharide-induced anxiety-like behavior by attenuating YAP-mediated neuro-inflammation and promoting hippocampal autophagy in mice

被引:22
作者
Tian, Qiuyun [1 ]
Fan, Xiaofang [1 ]
Ma, Jianshe [1 ]
Han, Yujiao [1 ]
Li, Dantong [1 ]
Jiang, Shan [1 ]
Zhang, Fukun [1 ]
Guang, Hui [1 ]
Shan, Xiaoqiong [1 ]
Chen, Ran [1 ]
Wang, Ping [1 ]
Wang, Qing [1 ]
Yang, Jinge [2 ]
Wang, Yongyu [1 ]
Hu, Lianggang [1 ]
Shentu, Yangping [3 ]
Gong, Yongsheng [1 ]
Fan, Junming [1 ]
机构
[1] Wenzhou Med Univ, Sch Basic Med Sci, Inst Hypoxia Med, Wenzhou 325035, Zhejiang, Peoples R China
[2] Jiangxi Med Coll, Dept Med Technol, Shangrao 334709, Jiangxi, Peoples R China
[3] Wenzhou Med Univ, Affiliated Hosp 1, Dept Pathol, Wenzhou 325000, Zhejiang, Peoples R China
基金
中国国家自然科学基金;
关键词
Resveratrol; Lipopolysaccharide; Anxiety-like behavior; Autophagy; Yes-associated protein; DEPRESSIVE-LIKE BEHAVIOR; NF-KAPPA-B; MAMMALIAN AUTOPHAGY; SEX-DIFFERENCES; SIRT1; PROTECTS; HIPPO PATHWAY; MICROGLIA; ACTIVATION; STRESS; NEUROINFLAMMATION;
D O I
10.1016/j.taap.2020.115261
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Resveratrol, a type of natural polyphenol mainly extracted from the skin of grapes, has been reported to protect against inflammatory responses and exert anxiolytic effect. Yes-associated protein (YAP), a major downstream effector of the Hippo signaling pathway, plays a critical role in inflammation. The present study aimed to explore whether YAP pathway was involved in the anxiolytic effect of resveratrol in lipopolysaccharide (LPS)-treated C57BL/6J male mice. LPS treatment induced anxiety-like behavior and decreased sirtuin 1 while increased YAP expression in the hippocampus. Resveratrol attenuated LPS-induced anxiety-like behavior, which was blocked by EX-527 (a sirtuin 1 inhibitor). Mechanistically, the anxiolytic effects of resveratrol were accompanied by a marked decrease in YAP, interleukin-1 beta and ionized calcium binding adaptor molecule 1 (Iba-1) while a significant increase in autophagic protein expression in the hippocampus. Pharmacological study using XMU-MP-1, a YAP activator, showed that activating YAP could induce anxiety-like behavior and neuro-inflammation as well as decrease hippocampal autophagy. Moreover, activation of YAP by XMU-MP-1 treatment attenuated the ameliorative effects of resveratrol on LPS-induced anxiety-like behavior, while blockade of YAP activation with verteporfin, a YAP inhibitor, attenuated LPS-induced anxiety-like behavior and neuro-inflammation as well as hippocampal autophagy. Finally, rapamycin-mediated promotion of autophagy attenuated LPS-induced anxiety like behavior and decreased interleukin-1 beta and Iba-1 expression in the hippocampus. Collectively, these results indicate that amelioration by resveratrol in LPS-induced anxiety-like behavior is through attenuating YAP mediated neuro-inflammation and promoting hippocampal autophagy, and suggest that inhibition of YAP pathway could be a potential therapeutic target for anxiety-like behavior induced by neuro-inflammation.
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页数:14
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