Metformin Alters Upper Small Intestinal Microbiota that Impact a Glucose-SGLT1-Sensing Glucoregulatory Pathway

Cell Metab. 2018 Jan 9;27(1):101-117.e5. doi: 10.1016/j.cmet.2017.09.019. Epub 2017 Oct 19.

Abstract

The gut microbiota alters energy homeostasis. In parallel, metformin regulates upper small intestinal sodium glucose cotransporter-1 (SGLT1), but whether changes of the microbiota or SGLT1-dependent pathways in the upper small intestine mediate metformin action is unknown. Here we report that upper small intestinal glucose sensing triggers an SGLT1-dependent pathway to lower glucose production in rodents. High-fat diet (HFD) feeding reduces glucose sensing and SGLT1 expression in the upper small intestine. Upper small intestinal metformin treatment restores SGLT1 expression and glucose sensing while shifting the upper small intestinal microbiota partly by increasing the abundance of Lactobacillus. Transplantation of upper small intestinal microbiota from metformin-treated HFD rats to the upper small intestine of untreated HFD rats also increases the upper small intestinal abundance of Lactobacillus and glucose sensing via an upregulation of SGLT1 expression. Thus, we demonstrate that metformin alters upper small intestinal microbiota and impacts a glucose-SGLT1-sensing glucoregulatory pathway.

Keywords: metformin; nutrient sensing; upper small intestinal microbiota.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Diet, High-Fat
  • Feeding Behavior
  • Gastrointestinal Microbiome / drug effects*
  • Glucagon-Like Peptide 1 / metabolism
  • Glucagon-Like Peptide-1 Receptor / metabolism
  • Glucose / metabolism*
  • Intestine, Small / drug effects
  • Intestine, Small / metabolism
  • Intestine, Small / microbiology
  • Metformin / pharmacology*
  • Principal Component Analysis
  • Rats
  • Sodium-Glucose Transporter 1 / metabolism*

Substances

  • Glucagon-Like Peptide-1 Receptor
  • Sodium-Glucose Transporter 1
  • Glucagon-Like Peptide 1
  • Metformin
  • Glucose

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