High fat diet-induced obesity leads to depressive and anxiety-like behaviors in mice via AMPK/mTOR-mediated autophagy

自噬 安普克 PI3K/AKT/mTOR通路 内分泌学 内科学 小胶质细胞 脂质代谢 神经炎症 磷酸化 医学 生物 炎症 信号转导 蛋白激酶A 细胞生物学 生物化学 细胞凋亡
作者
Yong Li,Yujie Cheng,Yuan Zhou,Hongmei Du,Cui Zhang,Zhentao Zhao,Yuenan Chen,Zhongnan Zhou,Jinyu Mei,Wen Li Wu,Ming Chen
出处
期刊:Experimental Neurology [Elsevier]
卷期号:348: 113949-113949 被引量:49
标识
DOI:10.1016/j.expneurol.2021.113949
摘要

Depression is one of the most common mental illnesses in modern society. In recent years, several studies show that there are disturbances in lipid metabolism in depressed patients. High-fat diet may lead to anxiety and depression, but the mechanisms involved remain unclear. In our study, we found that 8 weeks of high-fat feeding effectively induced metabolic disorders, including obesity and hyperlipidemia in mice. Interestingly, the mice also showed depressive and anxiety-like behaviors. We further found activated microglia and astrocyte, increased neuroinflammation, decreased autophagy and BDNF levels in mice after high-fat feeding. Besides, high-fat feeding can also inhibit AMPK phosphorylation and induce mTOR phosphorylation. After treating with the mTOR inhibitor rapamycin, autophagy and BDNF levels were elevated. The number of activated microglia and astrocyte, and pro-inflammation levels were reduced. Besides, rapamycin can also reduce the body weight and serum lipid level in high fat feeding mice. Depressive and anxiety-like behaviors were also ameliorated to some extent after rapamycin treatment. In summary, these results suggest that high-fat diet-induced obesity may lead to depressive and anxiety-like behaviors in mice by inhibiting AMPK phosphorylation and promoting mTOR shift to phosphorylation to inhibit autophagy. Therefore, improving lipid metabolism or enhancing autophagy through the AMPK/mTOR pathway could be potential targets for the treatment of obesity depression.
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