Modulation of the gut microbiota by metformin improves metabolic profiles in aged obese mice

Gut Microbes. 2018 Mar 4;9(2):155-165. doi: 10.1080/19490976.2017.1405209. Epub 2018 Feb 13.

Abstract

The gut microbiota is a contributing factor in obesity-related metabolic disorders. The effect of metformin on the gut microbiota has been reported; however, the relationship between the gut microbiota and the mechanism of action of metformin in elderly individuals is unclear. In this study, the effect of metformin on the gut microbiota was investigated in aged obese mice. The abundance of the genera Akkermansia, Bacteroides, Butyricimonas, and Parabacteroides was significantly increased by metformin in mice fed a high-fat diet. Metformin treatment decreased the expression of IL-1β and IL-6 in epididymal fat, which was correlated with the abundance of various bacterial genera. In addition, both fecal microbiota transplantation from metformin-treated mice and extracellular vesicles of Akkermansia muciniphila improved the body weight and lipid profiles of the mice. Our findings suggest that modulation of the gut microbiota by metformin results in metabolic improvements in aged mice, and that these effects are associated with inflammatory immune responses.

Keywords: Akkermansia muciniphila; aged mice; extracellular vesicles; gut microbiota; metformin.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Age Factors
  • Animals
  • Bacteria / classification
  • Bacteria / drug effects
  • Blood Glucose / drug effects
  • Body Weight / drug effects
  • Diet, High-Fat / adverse effects*
  • Disease Models, Animal
  • Epididymis / drug effects
  • Epididymis / immunology*
  • Feces / microbiology
  • Gastrointestinal Microbiome / drug effects*
  • Gastrointestinal Microbiome / physiology
  • Gene Expression Regulation / immunology
  • Interleukin-1beta / genetics
  • Interleukin-6 / genetics
  • Lipid Metabolism / drug effects
  • Male
  • Metformin / pharmacology*
  • Metformin / therapeutic use
  • Mice
  • Mice, Inbred C57BL
  • Obesity / drug therapy
  • Obesity / immunology
  • Obesity / metabolism*
  • Obesity / microbiology*

Substances

  • Blood Glucose
  • Interleukin-1beta
  • Interleukin-6
  • Metformin

Grants and funding

This work was supported by Korea Institute of Planning & Evaluation for Technology in Food, Agriculture, Forestry and Fisheries (iPET) (314044-3).