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The Origin and Understanding of the Incretin Concept

Gastrointestinal hormones that stimulate insulin secretion at physiological concentrations are incretins. This concept has recently attracted considerable attention in the wake of drugs developed from the gut hormone GLP-1 (glucagon-like peptide-1) for diabetes therapy. But the renewed enthusiasm ha...

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Autor principal: Rehfeld, Jens F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6054964/
https://www.ncbi.nlm.nih.gov/pubmed/30061863
http://dx.doi.org/10.3389/fendo.2018.00387
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author Rehfeld, Jens F.
author_facet Rehfeld, Jens F.
author_sort Rehfeld, Jens F.
collection PubMed
description Gastrointestinal hormones that stimulate insulin secretion at physiological concentrations are incretins. This concept has recently attracted considerable attention in the wake of drugs developed from the gut hormone GLP-1 (glucagon-like peptide-1) for diabetes therapy. But the renewed enthusiasm has also restricted the concept to just two hormones, GLP-1 and GIP (glucose-dependent insulinotropic polypeptide). The purpose of the present overview is two-fold: First to tell that the incretin concept is far from new. It has a more than a century long history full of ups and downs. Second, that the incretin concept may now have become too narrow. Thus, it is likely that incretin comprises additional gastrointestinal hormones, which interact with GIP and GLP-1 during normal meals containing protein, fat and complex carbohydrates (and not just pure glucose). Such broader incretin concept may stimulate development of novel gut hormone-derived drugs.
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spelling pubmed-60549642018-07-30 The Origin and Understanding of the Incretin Concept Rehfeld, Jens F. Front Endocrinol (Lausanne) Endocrinology Gastrointestinal hormones that stimulate insulin secretion at physiological concentrations are incretins. This concept has recently attracted considerable attention in the wake of drugs developed from the gut hormone GLP-1 (glucagon-like peptide-1) for diabetes therapy. But the renewed enthusiasm has also restricted the concept to just two hormones, GLP-1 and GIP (glucose-dependent insulinotropic polypeptide). The purpose of the present overview is two-fold: First to tell that the incretin concept is far from new. It has a more than a century long history full of ups and downs. Second, that the incretin concept may now have become too narrow. Thus, it is likely that incretin comprises additional gastrointestinal hormones, which interact with GIP and GLP-1 during normal meals containing protein, fat and complex carbohydrates (and not just pure glucose). Such broader incretin concept may stimulate development of novel gut hormone-derived drugs. Frontiers Media S.A. 2018-07-16 /pmc/articles/PMC6054964/ /pubmed/30061863 http://dx.doi.org/10.3389/fendo.2018.00387 Text en Copyright © 2018 Rehfeld. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Endocrinology
Rehfeld, Jens F.
The Origin and Understanding of the Incretin Concept
title The Origin and Understanding of the Incretin Concept
title_full The Origin and Understanding of the Incretin Concept
title_fullStr The Origin and Understanding of the Incretin Concept
title_full_unstemmed The Origin and Understanding of the Incretin Concept
title_short The Origin and Understanding of the Incretin Concept
title_sort origin and understanding of the incretin concept
topic Endocrinology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6054964/
https://www.ncbi.nlm.nih.gov/pubmed/30061863
http://dx.doi.org/10.3389/fendo.2018.00387
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