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Potential roles of GPR120 and its agonists in the management of diabetes

Free fatty acids (FFAs) serve not only as nutrients that provide energy but also as extracellular signaling molecules that manipulate intracellular physiological events through FFA receptors (FFARs) such as FFAR4. FFAR4 is also known as G-protein coupled receptor 120 (GPR120). The main role of GPR12...

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Autores principales: Zhang, Dan, Leung, Po Sing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4122337/
https://www.ncbi.nlm.nih.gov/pubmed/25114508
http://dx.doi.org/10.2147/DDDT.S53892
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author Zhang, Dan
Leung, Po Sing
author_facet Zhang, Dan
Leung, Po Sing
author_sort Zhang, Dan
collection PubMed
description Free fatty acids (FFAs) serve not only as nutrients that provide energy but also as extracellular signaling molecules that manipulate intracellular physiological events through FFA receptors (FFARs) such as FFAR4. FFAR4 is also known as G-protein coupled receptor 120 (GPR120). The main role of GPR120 is to elicit FFA regulation on metabolism homeostasis. GPR120 agonism correlates with prevention of the occurrence and development of metabolic disorders such as obesity and diabetes. GPR120 activation directly or indirectly inhibits inflammation, modulates hormone secretion from the gastrointestinal tract and pancreas, and regulates lipid and/or glucose metabolism in adipose, liver, and muscle tissues, which may help prevent obesity and diabetes. This review summarizes recent advances in physiological roles of GPR120 in preventing insulin resistance and protecting pancreatic islet function, and examines how resident GPR120 in the pancreas may be involved in modulating pancreatic islet function.
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spelling pubmed-41223372014-08-11 Potential roles of GPR120 and its agonists in the management of diabetes Zhang, Dan Leung, Po Sing Drug Des Devel Ther Review Free fatty acids (FFAs) serve not only as nutrients that provide energy but also as extracellular signaling molecules that manipulate intracellular physiological events through FFA receptors (FFARs) such as FFAR4. FFAR4 is also known as G-protein coupled receptor 120 (GPR120). The main role of GPR120 is to elicit FFA regulation on metabolism homeostasis. GPR120 agonism correlates with prevention of the occurrence and development of metabolic disorders such as obesity and diabetes. GPR120 activation directly or indirectly inhibits inflammation, modulates hormone secretion from the gastrointestinal tract and pancreas, and regulates lipid and/or glucose metabolism in adipose, liver, and muscle tissues, which may help prevent obesity and diabetes. This review summarizes recent advances in physiological roles of GPR120 in preventing insulin resistance and protecting pancreatic islet function, and examines how resident GPR120 in the pancreas may be involved in modulating pancreatic islet function. Dove Medical Press 2014-07-29 /pmc/articles/PMC4122337/ /pubmed/25114508 http://dx.doi.org/10.2147/DDDT.S53892 Text en © 2014 Zhang and Leung. This work is published by Dove Medical Press Limited, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License The full terms of the License are available at http://creativecommons.org/licenses/by-nc/3.0/. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Review
Zhang, Dan
Leung, Po Sing
Potential roles of GPR120 and its agonists in the management of diabetes
title Potential roles of GPR120 and its agonists in the management of diabetes
title_full Potential roles of GPR120 and its agonists in the management of diabetes
title_fullStr Potential roles of GPR120 and its agonists in the management of diabetes
title_full_unstemmed Potential roles of GPR120 and its agonists in the management of diabetes
title_short Potential roles of GPR120 and its agonists in the management of diabetes
title_sort potential roles of gpr120 and its agonists in the management of diabetes
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4122337/
https://www.ncbi.nlm.nih.gov/pubmed/25114508
http://dx.doi.org/10.2147/DDDT.S53892
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