High-Fat Proteins Drive Dynamic Changes in Gut Microbiota, Hepatic Metabolome, and Endotoxemia-TLR-4-NFκB-Mediated Inflammation in Mice

J Agric Food Chem. 2020 Oct 21;68(42):11710-11725. doi: 10.1021/acs.jafc.0c02570. Epub 2020 Oct 9.

Abstract

The responses of gut microbiota to dietary proteins have been studied previously. However, the effects of dietary proteins supplemented with a high-fat diet (HFD) on the metabolite biomarkers associated with non-alcoholic fatty liver disease (NAFLD) are not well understood. To understand the underlying mechanisms, C57BL/6J mice were fed with either a low-fat diet with casein (LFC) or an HFD with casein (HFC), fish (HFF), or mutton proteins (HFM), and their cecal microbiota and liver metabolites were analyzed. At the phylum level, the HFD group had a relatively higher abundance of Firmicutes compared to the LFC-diet group. At the genus level, the HFF-diet group had the highest abundance of Lactobacillus and Akkermansia compared to the HFC- and HFM-diet groups. Furthermore, mice fed with the HFF diet had significantly reduced levels of hepatic metabolites involved in oxidative stress and bile acid metabolism. Thus, meat proteins in HFD interact in the host to create distinct responses in the gut microbiota and its metabolites.

Keywords: gut microbiota; high-fat proteins; intestinal permeability; metabolites.

MeSH terms

  • Animals
  • Bacteria / classification
  • Bacteria / genetics
  • Bacteria / growth & development
  • Bacteria / isolation & purification
  • Bile Acids and Salts / metabolism
  • Diet, High-Fat / adverse effects
  • Dietary Proteins / adverse effects*
  • Dietary Proteins / metabolism
  • Endotoxemia / etiology
  • Endotoxemia / immunology*
  • Endotoxemia / metabolism
  • Endotoxemia / microbiology
  • Gastrointestinal Microbiome*
  • Humans
  • Liver / metabolism
  • Male
  • Mice
  • Mice, Inbred C57BL
  • NF-kappa B / genetics
  • NF-kappa B / immunology*
  • Oxidative Stress
  • Toll-Like Receptor 4 / genetics
  • Toll-Like Receptor 4 / immunology*

Substances

  • Bile Acids and Salts
  • Dietary Proteins
  • NF-kappa B
  • Toll-Like Receptor 4