Incrétines, sécrétion d'insuline et diabète


Autoria(s): Thorens, B.
Data(s)

01/09/2003

Resumo

Nutrient ingestion triggers a complex hormonal response aimed at stimulating glucose utilization in liver, muscle and adipose tissue to minimize the raise in blood glucose levels. Insulin secretion by pancreatic beta cells plays a major role in this response. Although the beta cell secretory response is mainly controlled by blood glucose levels, gut hormones secreted in response to food intake have an important role in potentiating glucose-stimulated insulin secretion. These gluco-incretin hormones are GLP-1 (glucagon-like peptide-1) and GIP (gluco-dependent insulinotropic polypeptide). Their action on pancreatic beta cells depends on binding to specific G-coupled receptors linked to activation of the adenylyl cyclase pathway. In addition to their effect on insulin secretion both hormones also stimulate insulin production at the transcriptional and translational level and positively regulate beta cell mass. Because the glucose-dependent insulinotropic action of GLP-1 is preserved in type 2 diabetic patients, this peptide is now developed as a novel therapeutic drug for this disease.

Identificador

https://serval.unil.ch/notice/serval:BIB_478FD742F151

info:pmid:14593618

pmid:14593618

isiid:000185269700019

Idioma(s)

fre

Fonte

Médecine sciences : M/S198-9860-863

Palavras-Chave #Animals; Diabetes Mellitus; Gastric Inhibitory Polypeptide; Glucagon; Glucagon-Like Peptide 1; Glucagon-Like Peptides; Humans; Insulin; Islets of Langerhans; Mice; Peptide Fragments; Protein Precursors; Rats
Tipo

info:eu-repo/semantics/review

article