Depression-like behaviors are accompanied by disrupted mitochondrial energy metabolism in chronic corticosterone-induced mice

代谢组 生物 SIRT3 线粒体 生物能学 皮质酮 脂质代谢 糖酵解 新陈代谢 西妥因1 内分泌学 氧化应激 内科学 柠檬酸循环 锡尔图因 生物化学 细胞生物学 NAD+激酶 激素 下调和上调 代谢物 基因 医学
作者
Xiaoxian Xie,Qichen Shen,Chunan Yu,Qingfeng Xiao,Jiafeng Zhou,Ze Xiong,Zezhi Li,Zhengwei Fu
出处
期刊:The Journal of Steroid Biochemistry and Molecular Biology [Elsevier BV]
卷期号:200: 105607-105607 被引量:47
标识
DOI:10.1016/j.jsbmb.2020.105607
摘要

Stress exerts its negative effects by interference with mitochondrial energy production in rodents, and is able to impair mitochondrial bioenergetics. However, the underlying mechanism that stress hormone impacts depression-like behaviors and mitochondrial energy metabolism is still not well understood. Here, we investigated the changes of depression-like behaviors and mitochondrial energy metabolism induced by chronic corticosterone (CORT). The results showed that after treatment with CORT for 6 weeks, mice displayed depression-like behaviors, which were identified by tail suspension test, forced swimming test and open field test. Then, the livers were isolated and tested by RNA sequencing and metabolome analysis. RNA sequencing showed 354 up-regulated genes and 284 down-regulated genes, and metabolome analysis revealed 280 metabolites with increased abundances and 193 metabolites with reduced abundances in the liver of mice after CORT, which were closely associated with lipid metabolism and oxidative phosphorylation in mitochondria. Based on these findings, the changes of mitochondrial energy metabolism were investigated, and we revealed that CORT condition inhibited glycolysis and fatty acid degradation pathway, and activated synthesis of triacylglycerol, leading to the reduced levels of acetyl-CoA and attenuated TCA cycle. Also, the pathways of NAD+ synthesis were inhibited, resulting in the reduced activity of sirtuin 3 (SIRT3). Thus, all of these observations disrupted the function of mitochondria, and led to the decrease of ATP production. Our findings uncover a novel mechanism of stress on depression-like behaviors and mitochondrial energy metabolism in rodents.
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