Ingestion of resistant starch by mice markedly increases microbiome-derived metabolites

FASEB J. 2019 Jul;33(7):8033-8042. doi: 10.1096/fj.201900177R. Epub 2019 Mar 29.

Abstract

Recent research has shown significant health benefits deriving from high-dietary fiber or microbiome-accessible carbohydrate consumption. Compared with native starch (NS), dietary resistant starch (RS) is a high microbiome-accessible carbohydrate that significantly alters the gut microbiome. The aim of this study was to determine the systemic metabolic effects of high microbiome-accessible carbohydrate. Male C57BL/6 mice were divided into 2 groups and fed either NS or RS for 18 wk (n = 20/group). Metabolomic analyses revealed that plasma levels of numerous metabolites were significantly different between the RS-fed and NS-fed mice, many of which are microbiome-derived. Most strikingly, we observed a 22-fold increase in gut microbiome-derived tryptophan metabolite indole-3-propionate (IPA), which was positively correlated with several gut microbiota, including Allobaculum, Bifidobacterium, and Lachnospiraceae, with Allobaculum having the most consistently increased abundance of all the IPA-associated taxa across all RS-fed mice. In addition, major changes were observed for metabolites solely or primarily metabolized in the gut (e.g., trimethylamine-N-oxide), metabolites that have a significant entero-hepatic circulation (i.e., bile acids), lipid metabolites (e.g., cholesterol sulfate), metabolites indicating increased energy turnover (e.g., tricarboxylic acid cycle intermediates and ketone bodies), and increased antioxidants such as reduced glutathione. Our findings reveal potentially novel mediators of high microbiome-accessible carbohydrate-derived health benefits.-Koay,Y. C., Wali. J. A., Luk, A. W. S., Macia, L., Cogger, V. C., Pulpitel, T. J., Wahl, D., Solon-Biet, S. M., Holmes, A., Simpson, S. J., O'Sullivan, J. F. Ingestion of resistant starch by mice markedly increases microbiome-derived metabolites.

Keywords: gut microbiome; metabolomics; microbiome-accessible carbohydrate; plasma.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animal Feed
  • Animals
  • Bacteria / metabolism
  • Bile Acids and Salts / metabolism
  • Chromatography, Liquid
  • Gastrointestinal Microbiome*
  • Hydrophobic and Hydrophilic Interactions
  • Indoles / blood
  • Lipids / blood
  • Male
  • Metabolome
  • Methylamines / blood
  • Mice
  • Mice, Inbred C57BL
  • Solubility
  • Starch / pharmacokinetics
  • Starch / pharmacology*
  • Tandem Mass Spectrometry

Substances

  • Bile Acids and Salts
  • Indoles
  • Lipids
  • Methylamines
  • indolepropionic acid
  • Starch
  • trimethyloxamine