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GLP-1 based therapeutics: simultaneously combating T2DM and obesity
Glucagon-like peptide-1 (GLP-1) enhances meal-related insulin secretion, which lowers blood glucose excursions. In addition to its incretin action, GLP-1 acts on the GLP-1 receptor (GLP-1R) in the brain to suppress feeding. These combined actions of GLP-1R signaling cause improvements in glycemic co...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2015
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4367528/ https://www.ncbi.nlm.nih.gov/pubmed/25852463 http://dx.doi.org/10.3389/fnins.2015.00092 |
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author | Heppner, Kristy M. Perez-Tilve, Diego |
author_facet | Heppner, Kristy M. Perez-Tilve, Diego |
author_sort | Heppner, Kristy M. |
collection | PubMed |
description | Glucagon-like peptide-1 (GLP-1) enhances meal-related insulin secretion, which lowers blood glucose excursions. In addition to its incretin action, GLP-1 acts on the GLP-1 receptor (GLP-1R) in the brain to suppress feeding. These combined actions of GLP-1R signaling cause improvements in glycemic control as well as weight loss in type II diabetes (T2DM) patients treated with GLP-1R agonists. This is a superior advantage of GLP-1R pharmaceuticals as many other drugs used to treat T2DM are weight neutral or actual cause weight gain. This review summarizes GLP-1R action on energy and glucose metabolism, the effectiveness of current GLP-1R agonists on weight loss in T2DM patients, as well as GLP-1R combination therapies. |
format | Online Article Text |
id | pubmed-4367528 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-43675282015-04-07 GLP-1 based therapeutics: simultaneously combating T2DM and obesity Heppner, Kristy M. Perez-Tilve, Diego Front Neurosci Endocrinology Glucagon-like peptide-1 (GLP-1) enhances meal-related insulin secretion, which lowers blood glucose excursions. In addition to its incretin action, GLP-1 acts on the GLP-1 receptor (GLP-1R) in the brain to suppress feeding. These combined actions of GLP-1R signaling cause improvements in glycemic control as well as weight loss in type II diabetes (T2DM) patients treated with GLP-1R agonists. This is a superior advantage of GLP-1R pharmaceuticals as many other drugs used to treat T2DM are weight neutral or actual cause weight gain. This review summarizes GLP-1R action on energy and glucose metabolism, the effectiveness of current GLP-1R agonists on weight loss in T2DM patients, as well as GLP-1R combination therapies. Frontiers Media S.A. 2015-03-20 /pmc/articles/PMC4367528/ /pubmed/25852463 http://dx.doi.org/10.3389/fnins.2015.00092 Text en Copyright © 2015 Heppner and Perez-Tilve. 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) or licensor 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 Heppner, Kristy M. Perez-Tilve, Diego GLP-1 based therapeutics: simultaneously combating T2DM and obesity |
title | GLP-1 based therapeutics: simultaneously combating T2DM and obesity |
title_full | GLP-1 based therapeutics: simultaneously combating T2DM and obesity |
title_fullStr | GLP-1 based therapeutics: simultaneously combating T2DM and obesity |
title_full_unstemmed | GLP-1 based therapeutics: simultaneously combating T2DM and obesity |
title_short | GLP-1 based therapeutics: simultaneously combating T2DM and obesity |
title_sort | glp-1 based therapeutics: simultaneously combating t2dm and obesity |
topic | Endocrinology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4367528/ https://www.ncbi.nlm.nih.gov/pubmed/25852463 http://dx.doi.org/10.3389/fnins.2015.00092 |
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