Microbiota, metabolome, and immune alterations in obese mice fed a high-fat diet containing type 2 resistant starch

Mol Nutr Food Res. 2017 Nov;61(11). doi: 10.1002/mnfr.201700184. Epub 2017 Sep 6.

Abstract

Scope: We examined the intestinal and systemic responses to incorporating a type 2 resistant starch (RS) into a high fat diet fed to obese mice.

Methods and results: Diet-induced obese, C57BL/6J male mice were fed an HF diet without or with 20% (by weight) high-amylose maize resistant starch (HF-RS) for 6 weeks. Serum adiponectin levels were higher with RS consumption, but there were no differences in weight gain and adiposity. With HF-RS, the expression levels of ileal TLR2 and Reg3g and cecal occludin, TLR2, TLR4, NOD1 and NOD2 were induced; whereas colonic concentrations of the inflammatory cytokine IL-17A declined. The intestinal, serum, liver, and urinary metabolomes were also altered. HF-RS resulted in lower amino acid concentrations, including lower serum branched chain amino acids, and increased quantities of urinary di/trimethylamine, 3-indoxylsulfate, and phenylacetylglycine. Corresponding to these changes were enrichments in Bacteroidetes (S24-7 family) and certain Firmicutes taxa (Lactobacillales and Erysipelotrichaceae) with the HF-RS diet. Parabacteroides and S24-7 positively associated with cecal maltose concentrations. These taxa and Erysipelotrichaceae, Allobaculum, and Bifidobacterium were directly correlated with uremic metabolites.

Conclusion: Consumption of RS modified the intestinal microbiota, stimulated intestinal immunity and endocrine-responses, and modified systemic metabolomes in obese mice consuming an otherwise obesogenic diet.

Keywords: High-fat diet; Metabolomics; Microbiota; Obesity; Resistant starch.

Publication types

  • Comparative Study

MeSH terms

  • Adiponectin / blood
  • Animals
  • Bacteroidetes / growth & development
  • Bacteroidetes / immunology
  • Bacteroidetes / isolation & purification
  • Bacteroidetes / physiology
  • Biomarkers / blood
  • Biomarkers / metabolism
  • Biomarkers / urine
  • Cecum / immunology
  • Cecum / metabolism
  • Cecum / microbiology
  • Diet, Carbohydrate Loading / adverse effects*
  • Diet, High-Fat / adverse effects*
  • Digestion
  • Dysbiosis / etiology*
  • Dysbiosis / immunology
  • Dysbiosis / metabolism
  • Dysbiosis / microbiology
  • Firmicutes / growth & development
  • Firmicutes / immunology
  • Firmicutes / isolation & purification
  • Firmicutes / physiology
  • Gene Expression Profiling
  • Gene Expression Regulation
  • Ileum / immunology
  • Ileum / metabolism
  • Ileum / microbiology
  • Immunity, Mucosal*
  • Intestinal Mucosa / immunology
  • Intestinal Mucosa / metabolism
  • Intestinal Mucosa / microbiology*
  • Liver / immunology
  • Liver / metabolism
  • Male
  • Metabolomics / methods
  • Mice, Inbred C57BL
  • Obesity / etiology*
  • Obesity / immunology
  • Obesity / metabolism
  • Obesity / microbiology
  • Principal Component Analysis
  • Resistant Starch
  • Starch / adverse effects
  • Starch / analogs & derivatives*
  • Starch / metabolism

Substances

  • Adiponectin
  • Adipoq protein, rat
  • Biomarkers
  • Resistant Starch
  • high-amylose maize type 2 resistant starch, maize
  • Starch