Anti-diabetic treatment leads to changes in gut microbiome

Front Biosci (Landmark Ed). 2019 Mar 1;24(4):688-699. doi: 10.2741/4743.

Abstract

Numerous micro-organisms naturally reside in the human body assuming a symbiotic, or, at times, even a dysbiotic relationship with the host. These microbial populations are referred to as the human microbiota. Host microbial populations are an important mediator of gastro-intestinal mucosal permeability, bile acid metabolism, short-chain fatty acids synthesis, fermentation of dietary polysaccharides and FXR/TGR5 signaling. Variations in the composition and function of gut microbiota have been observed in type 2 diabetes mellitus, insulin resistance and obesity, as well as in inflammatory bowel diseases. The microbial imbalance induced by such pathological processes is described as dysbiosis. In this review, we describe the pathophysiological links between type 2 diabetes mellitus and gut microbiota, explore the effect of anti-diabetic drugs on gut microbiota and suggest possible therapeutic targets.

Publication types

  • Review

MeSH terms

  • Animals
  • Diabetes Mellitus, Type 2 / drug therapy*
  • Diabetes Mellitus, Type 2 / microbiology
  • Dipeptidyl Peptidase 4 / metabolism
  • Dipeptidyl-Peptidase IV Inhibitors / pharmacology
  • Dysbiosis / chemically induced
  • Fermentation
  • Gastrointestinal Microbiome / drug effects*
  • Glucagon-Like Peptide 1 / agonists
  • Humans
  • Hypoglycemic Agents / pharmacology*
  • Incretins / metabolism
  • Insulin Resistance
  • Lipid Metabolism
  • Metformin / pharmacology
  • Mice
  • Obesity / metabolism
  • Permeability
  • Polysaccharides / metabolism
  • Signal Transduction
  • Sodium-Glucose Transporter 2 Inhibitors / pharmacology
  • alpha-Glucosidases / metabolism

Substances

  • Dipeptidyl-Peptidase IV Inhibitors
  • Hypoglycemic Agents
  • Incretins
  • Polysaccharides
  • Sodium-Glucose Transporter 2 Inhibitors
  • Glucagon-Like Peptide 1
  • Metformin
  • alpha-Glucosidases
  • DPP4 protein, human
  • Dipeptidyl Peptidase 4