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Glucagon‐like peptide‐1 (GLP‐1) signalling in the brain: From neural circuits and metabolism to therapeutics
Glucagon‐like‐peptide‐1 (GLP‐1) derived from gut enteroendocrine cells and a discrete population of neurons in the caudal medulla acts through humoral and neural pathways to regulate satiety, gastric motility and pancreatic endocrine function. These physiological attributes contribute to GLP‐1 havin...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8820188/ https://www.ncbi.nlm.nih.gov/pubmed/34519026 http://dx.doi.org/10.1111/bph.15682 |
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author | Kabahizi, Anita Wallace, Briana Lieu, Linh Chau, Dominic Dong, Yanbin Hwang, Eun‐Sang Williams, Kevin W. |
author_facet | Kabahizi, Anita Wallace, Briana Lieu, Linh Chau, Dominic Dong, Yanbin Hwang, Eun‐Sang Williams, Kevin W. |
author_sort | Kabahizi, Anita |
collection | PubMed |
description | Glucagon‐like‐peptide‐1 (GLP‐1) derived from gut enteroendocrine cells and a discrete population of neurons in the caudal medulla acts through humoral and neural pathways to regulate satiety, gastric motility and pancreatic endocrine function. These physiological attributes contribute to GLP‐1 having a potent therapeutic action in glycaemic regulation and chronic weight management. In this review, we provide an overview of the neural circuits targeted by endogenous versus exogenous GLP‐1 and related drugs. We also highlight candidate subpopulations of neurons and cellular mechanisms responsible for the acute and chronic effects of GLP‐1 and GLP‐1 receptor agonists on energy balance and glucose metabolism. Finally, we present potential future directions to translate these findings towards the development of effective therapies for treatment of metabolic disease. LINKED ARTICLES: This article is part of a themed issue on GLP1 receptor ligands (BJP 75th Anniversary). To view the other articles in this section visit http://onlinelibrary.wiley.com/doi/10.1111/bph.v179.4/issuetoc |
format | Online Article Text |
id | pubmed-8820188 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-88201882022-02-11 Glucagon‐like peptide‐1 (GLP‐1) signalling in the brain: From neural circuits and metabolism to therapeutics Kabahizi, Anita Wallace, Briana Lieu, Linh Chau, Dominic Dong, Yanbin Hwang, Eun‐Sang Williams, Kevin W. Br J Pharmacol GLP1 RECEPTOR LIGANDS (BJP 75th ANNIVERSARY) ‐ THEMED ISSUE REVIEWS Glucagon‐like‐peptide‐1 (GLP‐1) derived from gut enteroendocrine cells and a discrete population of neurons in the caudal medulla acts through humoral and neural pathways to regulate satiety, gastric motility and pancreatic endocrine function. These physiological attributes contribute to GLP‐1 having a potent therapeutic action in glycaemic regulation and chronic weight management. In this review, we provide an overview of the neural circuits targeted by endogenous versus exogenous GLP‐1 and related drugs. We also highlight candidate subpopulations of neurons and cellular mechanisms responsible for the acute and chronic effects of GLP‐1 and GLP‐1 receptor agonists on energy balance and glucose metabolism. Finally, we present potential future directions to translate these findings towards the development of effective therapies for treatment of metabolic disease. LINKED ARTICLES: This article is part of a themed issue on GLP1 receptor ligands (BJP 75th Anniversary). To view the other articles in this section visit http://onlinelibrary.wiley.com/doi/10.1111/bph.v179.4/issuetoc John Wiley and Sons Inc. 2021-11-04 2022-02 /pmc/articles/PMC8820188/ /pubmed/34519026 http://dx.doi.org/10.1111/bph.15682 Text en © 2021 The Authors. British Journal of Pharmacology published by John Wiley & Sons Ltd on behalf of British Pharmacological Society. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | GLP1 RECEPTOR LIGANDS (BJP 75th ANNIVERSARY) ‐ THEMED ISSUE REVIEWS Kabahizi, Anita Wallace, Briana Lieu, Linh Chau, Dominic Dong, Yanbin Hwang, Eun‐Sang Williams, Kevin W. Glucagon‐like peptide‐1 (GLP‐1) signalling in the brain: From neural circuits and metabolism to therapeutics |
title | Glucagon‐like peptide‐1 (GLP‐1) signalling in the brain: From neural circuits and metabolism to therapeutics |
title_full | Glucagon‐like peptide‐1 (GLP‐1) signalling in the brain: From neural circuits and metabolism to therapeutics |
title_fullStr | Glucagon‐like peptide‐1 (GLP‐1) signalling in the brain: From neural circuits and metabolism to therapeutics |
title_full_unstemmed | Glucagon‐like peptide‐1 (GLP‐1) signalling in the brain: From neural circuits and metabolism to therapeutics |
title_short | Glucagon‐like peptide‐1 (GLP‐1) signalling in the brain: From neural circuits and metabolism to therapeutics |
title_sort | glucagon‐like peptide‐1 (glp‐1) signalling in the brain: from neural circuits and metabolism to therapeutics |
topic | GLP1 RECEPTOR LIGANDS (BJP 75th ANNIVERSARY) ‐ THEMED ISSUE REVIEWS |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8820188/ https://www.ncbi.nlm.nih.gov/pubmed/34519026 http://dx.doi.org/10.1111/bph.15682 |
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