Ezcurra, Marina, Reimann, Frank, Gribble, Fiona M, Emery, Edward (2013) Molecular mechanisms of incretin hormone secretion. Current Opinion in Pharmacology, 13 (6). pp. 922-927. ISSN 1471-4892. (doi:10.1016/j.coph.2013.08.013) (KAR id:91125)
PDF
Publisher pdf
Language: English |
|
Download this file (PDF/926kB) |
Preview |
Request a format suitable for use with assistive technology e.g. a screenreader | |
Official URL: https://doi.org/10.1016/j.coph.2013.08.013 |
Abstract
Incretin peptides (glucagon-like peptide-1 (GLP-1) and glucose-dependent insulinotropic polypeptide (GIP)) are secreted from enteroendocrine cells in the intestinal epithelium, and help to coordinate metabolic responses to food ingestion. A number of molecular mechanisms have recently been defined that underlie carbohydrate, lipid and protein sensing in gut endocrine cells. Knockout mice lacking sodium glucose tranporter-1 (SGLT-1) or the short chain fatty acid sensing receptor FFAR2 (GPR43), for example, have highlighted the importance of these molecules in incretin secretion. This review outlines our current understanding of sensory pathways in incretin secreting cells and highlights the therapeutic potential of targeting them for the development of novel therapies for obesity and diabetes.
Item Type: | Article |
---|---|
DOI/Identification number: | 10.1016/j.coph.2013.08.013 |
Subjects: | Q Science > QP Physiology (Living systems) |
Divisions: | Divisions > Division of Natural Sciences > Biosciences |
Depositing User: | Marina Ezcurra |
Date Deposited: | 27 Oct 2021 16:18 UTC |
Last Modified: | 05 Nov 2024 12:56 UTC |
Resource URI: | https://kar.kent.ac.uk/id/eprint/91125 (The current URI for this page, for reference purposes) |
- Link to SensusAccess
- Export to:
- RefWorks
- EPrints3 XML
- BibTeX
- CSV
- Depositors only (login required):