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Molecular mechanisms of incretin hormone secretion()

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 t...

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Detalles Bibliográficos
Autores principales: Ezcurra, Marina, Reimann, Frank, Gribble, Fiona M, Emery, Edward
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Science Ltd 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3838618/
https://www.ncbi.nlm.nih.gov/pubmed/24035446
http://dx.doi.org/10.1016/j.coph.2013.08.013
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author Ezcurra, Marina
Reimann, Frank
Gribble, Fiona M
Emery, Edward
author_facet Ezcurra, Marina
Reimann, Frank
Gribble, Fiona M
Emery, Edward
author_sort Ezcurra, Marina
collection PubMed
description 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.
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spelling pubmed-38386182013-12-01 Molecular mechanisms of incretin hormone secretion() Ezcurra, Marina Reimann, Frank Gribble, Fiona M Emery, Edward Curr Opin Pharmacol Article 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. Elsevier Science Ltd 2013-12 /pmc/articles/PMC3838618/ /pubmed/24035446 http://dx.doi.org/10.1016/j.coph.2013.08.013 Text en © 2013 The Authors https://creativecommons.org/licenses/by-nc-nd/3.0/ Open Access under CC BY-NC-ND 3.0 (https://creativecommons.org/licenses/by-nc-nd/3.0/) license
spellingShingle Article
Ezcurra, Marina
Reimann, Frank
Gribble, Fiona M
Emery, Edward
Molecular mechanisms of incretin hormone secretion()
title Molecular mechanisms of incretin hormone secretion()
title_full Molecular mechanisms of incretin hormone secretion()
title_fullStr Molecular mechanisms of incretin hormone secretion()
title_full_unstemmed Molecular mechanisms of incretin hormone secretion()
title_short Molecular mechanisms of incretin hormone secretion()
title_sort molecular mechanisms of incretin hormone secretion()
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3838618/
https://www.ncbi.nlm.nih.gov/pubmed/24035446
http://dx.doi.org/10.1016/j.coph.2013.08.013
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