Literature DB >> 31923756

Daidzein promotes the expression of oxidative phosphorylation- and fatty acid oxidation-related genes via an estrogen-related receptor α pathway to decrease lipid accumulation in muscle cells.

Kanano Kitamura1, Jane Surya Erlangga1, Sakuka Tsukamoto1, Yuri Sakamoto2, Hideaki Mabashi-Asazuma3, Kaoruko Iida4.   

Abstract

Estrogen-related receptor (ERR)α regulates genes involved in fatty acid oxidation (FAO) and oxidative phosphorylation (OXPHOS) in muscle. The soy isoflavone daidzein was reported to be a putative ERRα activator, but little is known about its effects on gene expression and FA metabolism. This study aimed to clarify whether daidzein affects FAO- and OXPHOS-related genes thereby modulating intracellular FA metabolism in muscle cells. For this purpose, we used the C2C12 murine muscle cell line. ERRα-expressing C2C12 myotubes were treated with 50 μM daidzein, and gene expression was examined. The expression of FAO genes such as pyruvate dehydrogenase kinase 4 (Pdk4) and acyl-coenzyme A dehydrogenase (Acadm) and that of OXPHOS genes such as ATP synthase F1 subunit beta (Atp5b) and cytochrome c (Cycs) was significantly increased by daidzein, and these effects were partially blocked by an ERRα inhibitor. Using a reporter assay, we showed that daidzein enhanced the promoter activity of these genes and that ERRα responsive elements in the promoter region were necessary for the action of daidzein. Finally, daidzein significantly decreased lipid accumulation in C2C12 myotubes associated with increased oxygen consumption. In conclusion, daidzein decreases lipid deposition in muscle cells by regulating the expression of genes related to FAO and OXPHOS via an ERRα-associated pathway at least in part. These results suggest that daidzein would be a beneficial tool to protect against various diseases caused by muscle lipotoxicity.
Copyright © 2019 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Daidzein; Estrogen-related receptor α; Fatty acid oxidation; Oxidative phosphorylation; Skeletal muscle cells

Mesh:

Substances:

Year:  2019        PMID: 31923756     DOI: 10.1016/j.jnutbio.2019.108315

Source DB:  PubMed          Journal:  J Nutr Biochem        ISSN: 0955-2863            Impact factor:   6.048


  3 in total

1.  Kangtaizhi Granule Alleviated Nonalcoholic Fatty Liver Disease in High-Fat Diet-Fed Rats and HepG2 Cells via AMPK/mTOR Signaling Pathway.

Authors:  Jiaxin Zhang; Haixia Du; Menglan Shen; Zhengqi Zhao; Xinmiao Ye
Journal:  J Immunol Res       Date:  2020-08-20       Impact factor: 4.818

2.  Mdfi Promotes C2C12 Cell Differentiation and Positively Modulates Fast-to-Slow-Twitch Muscle Fiber Transformation.

Authors:  Bo Huang; Yiren Jiao; Yifan Zhu; Zuocheng Ning; Zijian Ye; Qing X Li; Chingyuan Hu; Chong Wang
Journal:  Front Cell Dev Biol       Date:  2021-01-22

3.  Declined expressions of vast mitochondria-related genes represented by CYCS and transcription factor ESRRA in skeletal muscle aging.

Authors:  Jingbao Kan; Yifang Hu; Yaoqi Ge; WenSong Zhang; Shan Lu; Cuiping Zhao; Rihua Zhang; Yun Liu
Journal:  Bioengineered       Date:  2021-12       Impact factor: 3.269

  3 in total

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