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Glucagon, GLP-1 and Thermogenesis
Brown adipose tissue (BAT) thermogenesis is a conserved mechanism to maintain body temperature in mammals. However, since BAT contribution to energy expenditure can represent a relevant modulator of metabolic homeostasis, many studies have focused on the nervous system and endocrine factors that con...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6678955/ https://www.ncbi.nlm.nih.gov/pubmed/31337027 http://dx.doi.org/10.3390/ijms20143445 |
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author | González-García, Ismael Milbank, Edward Diéguez, Carlos López, Miguel Contreras, Cristina |
author_facet | González-García, Ismael Milbank, Edward Diéguez, Carlos López, Miguel Contreras, Cristina |
author_sort | González-García, Ismael |
collection | PubMed |
description | Brown adipose tissue (BAT) thermogenesis is a conserved mechanism to maintain body temperature in mammals. However, since BAT contribution to energy expenditure can represent a relevant modulator of metabolic homeostasis, many studies have focused on the nervous system and endocrine factors that control the activity of this tissue. There is long-established evidence that the counter-regulatory hormone glucagon negatively influences energy balance, enhances satiety, and increases energy expenditure. Despite compelling evidence showing that glucagon has direct action on BAT thermogenesis, recent findings are questioning this conventional attribute of glucagon action. Glucagon like peptide-1 (GLP-1) is an incretin secreted by the intestinal tract which strongly decreases feeding, and, furthermore, improves metabolic parameters associated with obesity and diabetes. Therefore, GLP-1 receptors (GLP-1-R) have emerged as a promising target in the treatment of metabolic disorders. In this short review, we will summarize the latest evidence in this regard, as well as the current therapeutic glucagon- and GLP-1-based approaches to treating obesity. |
format | Online Article Text |
id | pubmed-6678955 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-66789552019-08-19 Glucagon, GLP-1 and Thermogenesis González-García, Ismael Milbank, Edward Diéguez, Carlos López, Miguel Contreras, Cristina Int J Mol Sci Review Brown adipose tissue (BAT) thermogenesis is a conserved mechanism to maintain body temperature in mammals. However, since BAT contribution to energy expenditure can represent a relevant modulator of metabolic homeostasis, many studies have focused on the nervous system and endocrine factors that control the activity of this tissue. There is long-established evidence that the counter-regulatory hormone glucagon negatively influences energy balance, enhances satiety, and increases energy expenditure. Despite compelling evidence showing that glucagon has direct action on BAT thermogenesis, recent findings are questioning this conventional attribute of glucagon action. Glucagon like peptide-1 (GLP-1) is an incretin secreted by the intestinal tract which strongly decreases feeding, and, furthermore, improves metabolic parameters associated with obesity and diabetes. Therefore, GLP-1 receptors (GLP-1-R) have emerged as a promising target in the treatment of metabolic disorders. In this short review, we will summarize the latest evidence in this regard, as well as the current therapeutic glucagon- and GLP-1-based approaches to treating obesity. MDPI 2019-07-13 /pmc/articles/PMC6678955/ /pubmed/31337027 http://dx.doi.org/10.3390/ijms20143445 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review González-García, Ismael Milbank, Edward Diéguez, Carlos López, Miguel Contreras, Cristina Glucagon, GLP-1 and Thermogenesis |
title | Glucagon, GLP-1 and Thermogenesis |
title_full | Glucagon, GLP-1 and Thermogenesis |
title_fullStr | Glucagon, GLP-1 and Thermogenesis |
title_full_unstemmed | Glucagon, GLP-1 and Thermogenesis |
title_short | Glucagon, GLP-1 and Thermogenesis |
title_sort | glucagon, glp-1 and thermogenesis |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6678955/ https://www.ncbi.nlm.nih.gov/pubmed/31337027 http://dx.doi.org/10.3390/ijms20143445 |
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