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Proteomic and microbial assessments on the effect of Antrodia cinnamomea in C57BL/6 mice.
Tsai, Yi-Ting; Ruan, Jhen-Wei; Chang, Cherng-Shyang; Ko, Mei-Lan; Chou, Hsiu-Chuan; Lin, Chi-Chien; Lin, Chiao-Mei; Huang, Chih-Ting; Wei, Yu-Shan; Liao, En-Chi; Chen, Hsin-Yi; Lin, Li-Hsun; Lin, Meng-Wei; Kao, Cheng-Yuan; Chan, Hong-Lin.
Affiliation
  • Tsai YT; Institute of Bioinformatics and Structural Biology, National Tsing Hua University, Hsinchu, 30013, Taiwan. Electronic address: peach19920722@gmail.com.
  • Ruan JW; Department of Medical Laboratory Science and Biotechnology, National Cheng Kung University, Tainan, 70101, Taiwan. Electronic address: jhenweiruan@mail.ncku.edu.tw.
  • Chang CS; Immunology Research Center, National Health Research Institutes, Zhunan, Miaoli, 35053, Taiwan. Electronic address: rebear0330@gmail.com.
  • Ko ML; Department of Ophthalmology, National Taiwan University Hospital Hsin-Chu Branch, Hsinchu, 30059, Taiwan. Electronic address: aaddch@gmail.com.
  • Chou HC; Department of Biomedical Engineering and Environmental Sciences, National Tsing Hua University, Hsinchu, 30013, Taiwan. Electronic address: chouhc@mx.nthu.edu.tw.
  • Lin CC; Department of Life Sciences, Institute of Biomedical Science, National Chung Hsing University, Taichung, 402, Taiwan. Electronic address: lincc@dragon.nchu.edu.tw.
  • Lin CM; Immunology Research Center, National Health Research Institutes, Zhunan, Miaoli, 35053, Taiwan. Electronic address: chiaomei@nhri.edu.tw.
  • Huang CT; Immunology Research Center, National Health Research Institutes, Zhunan, Miaoli, 35053, Taiwan. Electronic address: cindyhuang@nhri.edu.tw.
  • Wei YS; Institute of Bioinformatics and Structural Biology, National Tsing Hua University, Hsinchu, 30013, Taiwan. Electronic address: t91050127@hotmail.com.tw.
  • Liao EC; Institute of Bioinformatics and Structural Biology, National Tsing Hua University, Hsinchu, 30013, Taiwan. Electronic address: nakyla1215@gmail.com.
  • Chen HY; Institute of Bioinformatics and Structural Biology, National Tsing Hua University, Hsinchu, 30013, Taiwan. Electronic address: dful690@yahoo.com.tw.
  • Lin LH; Institute of Bioinformatics and Structural Biology, National Tsing Hua University, Hsinchu, 30013, Taiwan. Electronic address: lishlin0207@gmail.com.
  • Lin MW; Institute of Bioinformatics and Structural Biology, National Tsing Hua University, Hsinchu, 30013, Taiwan. Electronic address: eva1018cat@yahoo.com.tw.
  • Kao CY; Immunology Research Center, National Health Research Institutes, Zhunan, Miaoli, 35053, Taiwan. Electronic address: chengyuankao@nhri.edu.tw.
  • Chan HL; Institute of Bioinformatics and Structural Biology and Department of Medical Sciences, National Tsing Hua University, Hsinchu, 30013, Taiwan. Electronic address: hlchan@life.nthu.edu.tw.
Arch Biochem Biophys ; 713: 109058, 2021 11 30.
Article in En | MEDLINE | ID: mdl-34627749
ABSTRACT
Antrodia cinnamomea (AC) is a nutraceutical fungus and studies have suggested that AC has the potential to prevent or alleviate diseases. However, little is known about the AC-induced phenotypes on the intestine-liver axis and gut microbial alterations. Here, we performed two-dimensional difference gel electrophoresis (2D-DIGE) and MALDI-Biotyper to elaborate the AC-induced phenotypes on the intestine-liver axis and gut microbial distribution of C57BL/6 mice. The experimental outcomes showed that the hepatic density may increase by elevating hepatic redox regulation, lipid degradation and glycolysis-related proteins and alleviating cholesterol biosynthesis and transport-related proteins in C57BL/6 mice with AC treatment. Moreover, AC facilitates intestinal glycolysis, TCA cycle, redox and cytoskeleton regulation-related proteins, but also reduces intestinal vesicle transport-related proteins in C57BL/6 mice. However, the body weight, GTT, daily food/water intake, and fecal/urine weight were unaffected by AC supplementation in C57BL/6 mice. Notably, the C57BL/6-AC mice had a higher gut microbial abundance of Alistipes shahii (AS) than C57BL/6-Ctrl mice. In summary, the AC treatment affects intestinal permeability by regulating redox and cytoskeleton-related proteins and elevates the gut microbial abundance of AS in C57BL/6 mice that might be associated with increasing hepatic density and metabolism-related proteins of the liver in C57BL/6 mice. Our study provides an insight into the mechanisms of AC-induced phenotypes and a comprehensive assessment of AC's nutraceutical effect in C57BL/6 mice.
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Full text: 1 Database: MEDLINE Main subject: Dietary Supplements / Polyporales / Proteome / Gastrointestinal Microbiome Limits: Animals Language: En Year: 2021 Type: Article

Full text: 1 Database: MEDLINE Main subject: Dietary Supplements / Polyporales / Proteome / Gastrointestinal Microbiome Limits: Animals Language: En Year: 2021 Type: Article