GLUT2 and the incretin receptors are involved in glucose-induced incretin secretion
Research output: Contribution to journal › Journal article › Research › peer-review
Patrice D Cani, Jens Juul Holst, Daniel J Drucker, Nathalie M Delzenne, Bernard Thorens, Rémy Burcelin, Claude Knauf
Glucagon-like peptide-1 (GLP-1) and glucose-dependent insulinotropic polypeptide (GIP) are incretins secreted in response to oral glucose ingestion by intestinal L and K cells, respectively. The molecular mechanisms responsible for intestinal cell glucose sensing are unknown but could be related to those described for beta-cells, brain and hepatoportal sensors. We determined the role of GLUT2, GLP-1 or GIP receptors in glucose-induced incretins secretion, in the corresponding knockout mice. GLP-1 secretion was reduced in all mutant mice, while GIP secretion did not require GLUT2. Intestinal GLP-1 content was reduced only in GIP and GLUT2 receptors knockout mice suggesting that this impairment could contribute to the phenotype. Intestinal GIP content was similar in all mice studied. Furthermore, the impaired incretins secretion was associated with a reduced glucose-stimulated insulin secretion and an impaired glucose tolerance in all mice. In conclusion, both incretins secretion depends on mechanisms involving their own receptors and GLP-1 further requires GLUT2.
|Journal||Molecular and Cellular Endocrinology|
|Number of pages||6|
|Publication status||Published - 30 Sep 2007|
- Animals, Gastric Inhibitory Polypeptide, Glucagon-Like Peptide 1, Glucose, Glucose Intolerance, Glucose Tolerance Test, Glucose Transporter Type 2, Intestines, Mice, Mice, Knockout, Models, Biological, Portal System, Receptors, Gastrointestinal Hormone, Receptors, Glucagon