Anti-diabetic treatment leads to changes in gut microbiome.
Animals
Diabetes Mellitus, Type 2
/ drug therapy
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
Journal
Frontiers in bioscience (Landmark edition)
ISSN: 2768-6698
Titre abrégé: Front Biosci (Landmark Ed)
Pays: Singapore
ID NLM: 101612996
Informations de publication
Date de publication:
01 03 2019
01 03 2019
Historique:
entrez:
8
3
2019
pubmed:
8
3
2019
medline:
10
8
2019
Statut:
epublish
Résumé
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.
Substances chimiques
Dipeptidyl-Peptidase IV Inhibitors
0
Hypoglycemic Agents
0
Incretins
0
Polysaccharides
0
Sodium-Glucose Transporter 2 Inhibitors
0
Glucagon-Like Peptide 1
89750-14-1
Metformin
9100L32L2N
alpha-Glucosidases
EC 3.2.1.20
DPP4 protein, human
EC 3.4.14.5
Dipeptidyl Peptidase 4
EC 3.4.14.5
Types de publication
Journal Article
Review
Langues
eng