Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: González-García, Ismael, Milbank, Edward, Diéguez, Carlos, López, Miguel, Contreras, Cristina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
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
_version_ 1783441224934359040
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
work_keys_str_mv AT gonzalezgarciaismael glucagonglp1andthermogenesis
AT milbankedward glucagonglp1andthermogenesis
AT dieguezcarlos glucagonglp1andthermogenesis
AT lopezmiguel glucagonglp1andthermogenesis
AT contrerascristina glucagonglp1andthermogenesis