The G-Protein-Coupled Long-Chain Fatty Acid Receptor GPR40 and Glucose Metabolism

Free fatty acids (FFAs) play a pivotal role in metabolic control and cell signaling processes in various tissues. In particular, FFAs are known to augment glucose-stimulated insulin secretion by pancreatic beta cells, where fatty acid-derived metabolites, such as long-chain fatty acyl-CoAs, are beli...

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Published inFrontiers in endocrinology (Lausanne) Vol. 5; p. 152
Main Authors Tomita, Tsutomu, Hosoda, Kiminori, Fujikura, Junji, Inagaki, Nobuya, Nakao, Kazuwa
Format Journal Article
LanguageEnglish
Published Switzerland Frontiers Media S.A 01.01.2014
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Abstract Free fatty acids (FFAs) play a pivotal role in metabolic control and cell signaling processes in various tissues. In particular, FFAs are known to augment glucose-stimulated insulin secretion by pancreatic beta cells, where fatty acid-derived metabolites, such as long-chain fatty acyl-CoAs, are believed to act as crucial effectors. Recently, G-protein-coupled receptor 40 (GPR40), a receptor for long-chain fatty acids, was reported to be highly expressed in pancreatic beta cells and involved in the regulation of insulin secretion. Hence, GPR40 is considered to be a potential therapeutic target for the treatment of diabetes. In this review, we summarize the identification and gene expression patterns of GPR40 and its role in glucose metabolism. We also discuss the potential application of GPR40 as a therapeutic target.
AbstractList Free fatty acids (FFAs) play a pivotal role in metabolic control and cell signaling processes in various tissues. In particular, FFAs are known to augment glucose-stimulated insulin secretion by pancreatic beta cells, where fatty acid-derived metabolites, such as long-chain fatty acyl-CoAs, are believed to act as crucial effectors. Recently, G-protein-coupled receptor 40 (GPR40), a receptor for long-chain fatty acids, was reported to be highly expressed in pancreatic beta cells and involved in the regulation of insulin secretion. Hence, GPR40 is considered to be a potential therapeutic target for the treatment of diabetes. In this review, we summarize the identification and gene expression patterns of GPR40 and its role in glucose metabolism. We also discuss the potential application of GPR40 as a therapeutic target.
Free fatty acids (FFAs) play a pivotal role in metabolic control and cell signaling processes in various tissues. In particular, FFAs are known to augment glucose-stimulated insulin secretion (GSIS) by pancreatic beta cells, where fatty acid-derived metabolites, such as long chain fatty acyl-CoAs, are believed to act as crucial effectors. Recently, G-protein-coupled receptor 40 (GPR40), a receptor for long-chain fatty acids, was reported to be highly expressed in pancreatic beta cells and involved in the regulation of insulin secretion. Hence, GPR40 is considered to be a potential therapeutic target for the treatment of diabetes. In this review, we summarize the identification and gene expression patterns of GPR40 and its role in glucose metabolism. We also discuss the potential application of GPR40 as a therapeutic target.
Author Hosoda, Kiminori
Fujikura, Junji
Tomita, Tsutomu
Inagaki, Nobuya
Nakao, Kazuwa
AuthorAffiliation 2 Medical Innovation Center, Kyoto University Graduate School of Medicine , Kyoto , Japan
1 Department of Diabetes, Endocrinology and Nutrition, Kyoto University Graduate School of Medicine , Kyoto , Japan
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  surname: Nakao
  fullname: Nakao, Kazuwa
  organization: Medical Innovation Center, Kyoto University Graduate School of Medicine , Kyoto , Japan
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Keywords LCFA
pancreatic beta cells
FFAR1
GPR40
insulin secretion
Language English
License This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
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Edited by: Ikuo Kimura, Tokyo University of Agriculture and Technology, Japan
This article was submitted to Diabetes, a section of the journal Frontiers in Endocrinology.
Reviewed by: Carol Huang, University of Calgary, Canada; Kay Waud, Jones Institute for Reproductive Medicine, USA
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FFAR1
GPR40
insulin secretion
LCFA
pancreatic beta cells
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Title The G-Protein-Coupled Long-Chain Fatty Acid Receptor GPR40 and Glucose Metabolism
URI https://www.ncbi.nlm.nih.gov/pubmed/25309513
https://search.proquest.com/docview/1611617021
https://pubmed.ncbi.nlm.nih.gov/PMC4176464
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Volume 5
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