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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...

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Autores principales: Kabahizi, Anita, Wallace, Briana, Lieu, Linh, Chau, Dominic, Dong, Yanbin, Hwang, Eun‐Sang, Williams, Kevin W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
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
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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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