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

AbstractSCOPE:
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.
AuthorsJavad Barouei, Zach Bendiks, Alice Martinic, Darya Mishchuk, Dustin Heeney, Yu-Hsin Hsieh, Dorothy Kieffer, Jose Zaragoza, Roy Martin, Carolyn Slupsky, Maria L Marco
JournalMolecular nutrition & food research (Mol Nutr Food Res) Vol. 61 Issue 11 (11 2017) ISSN: 1613-4133 [Electronic] Germany
PMID28736992 (Publication Type: Comparative Study, Journal Article)
Copyright© 2017 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
Chemical References
  • Adiponectin
  • Adipoq protein, rat
  • Biomarkers
  • Resistant Starch
  • high-amylose maize type 2 resistant starch, maize
  • Starch
Topics
  • Adiponectin (blood)
  • Animals
  • Bacteroidetes (growth & development, immunology, isolation & purification, physiology)
  • Biomarkers (blood, metabolism, urine)
  • Cecum (immunology, metabolism, microbiology)
  • Diet, Carbohydrate Loading (adverse effects)
  • Diet, High-Fat (adverse effects)
  • Digestion
  • Dysbiosis (etiology, immunology, metabolism, microbiology)
  • Firmicutes (growth & development, immunology, isolation & purification, physiology)
  • Gene Expression Profiling
  • Gene Expression Regulation
  • Ileum (immunology, metabolism, microbiology)
  • Immunity, Mucosal
  • Intestinal Mucosa (immunology, metabolism, microbiology)
  • Liver (immunology, metabolism)
  • Male
  • Metabolomics (methods)
  • Mice, Inbred C57BL
  • Obesity (etiology, immunology, metabolism, microbiology)
  • Principal Component Analysis
  • Resistant Starch
  • Starch (adverse effects, analogs & derivatives, metabolism)

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