Literature DB >> 24315954

GPR120 agonism as a countermeasure against metabolic diseases.

Lauren M Cornall1, Michael L Mathai1, Deanne H Hryciw2, Andrew J McAinch3.   

Abstract

Obesity, type 2 diabetes mellitus and cardiovascular disease are at epidemic proportions in developed nations globally, representing major causes of ill-health and premature death. The search for drug targets to counter the growing prevalence of metabolic diseases has uncovered G-protein-coupled receptor 120 (GPR120). GPR120 agonism has been shown to improve inflammation and metabolic health on a systemic level via regulation of adiposity, gastrointestinal peptide secretion, taste preference and glucose homeostasis. Therefore, GPR120 agonists present as a novel therapeutic option that could be exploited for the treatment of impaired metabolic health. This review summarizes the current knowledge of GPR120 functionality and the potential applications of GPR120-specific agonists for the treatment of disease states such as obesity, type 2 diabetes mellitus and cardiovascular disease.
Copyright © 2013 Elsevier Ltd. All rights reserved.

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Year:  2013        PMID: 24315954     DOI: 10.1016/j.drudis.2013.11.021

Source DB:  PubMed          Journal:  Drug Discov Today        ISSN: 1359-6446            Impact factor:   7.851


  11 in total

1.  Therapeutic Potential of GPR120 Agonists for the Treatment of Type 2 Diabetes.

Authors:  Ahmed F Abdel-Magid
Journal:  ACS Med Chem Lett       Date:  2015-10-16       Impact factor: 4.345

Review 2.  ω3-Polyunsaturated fatty acids for heart failure: Effects of dose on efficacy and novel signaling through free fatty acid receptor 4.

Authors:  Timothy D O'Connell; Robert C Block; Shue P Huang; Gregory C Shearer
Journal:  J Mol Cell Cardiol       Date:  2016-12-14       Impact factor: 5.000

3.  Treatment with TUG891, a free fatty acid receptor 4 agonist, restores adipose tissue metabolic dysfunction following chronic sleep fragmentation in mice.

Authors:  D Gozal; Z Qiao; I Almendros; J Zheng; A Khalyfa; B Shimpukade; T Ulven
Journal:  Int J Obes (Lond)       Date:  2016-03-16       Impact factor: 5.095

4.  Role of GPR120 in cell motile activity induced by 12-O-tetradecanoylphorbol-13-acetate in liver epithelial WB-F344 cells.

Authors:  Shuhei Ishii; Miku Hirane; Yuka Kitamura; Shiori Mori; Nobuyuki Fukushima; Kanya Honoki; Toshifumi Tsujiuchi
Journal:  Mol Cell Biochem       Date:  2014-11-08       Impact factor: 3.396

5.  Probe-Dependent Negative Allosteric Modulators of the Long-Chain Free Fatty Acid Receptor FFA4.

Authors:  Kenneth R Watterson; Steffen V F Hansen; Brian D Hudson; Elisa Alvarez-Curto; Sheikh Zahir Raihan; Carlos M G Azevedo; Gabriel Martin; Julia Dunlop; Stephen J Yarwood; Trond Ulven; Graeme Milligan
Journal:  Mol Pharmacol       Date:  2017-04-06       Impact factor: 4.436

Review 6.  FFAR4: A New Player in Cardiometabolic Disease?

Authors:  Gage M Stuttgen; Daisy Sahoo
Journal:  Endocrinology       Date:  2021-08-01       Impact factor: 5.051

Review 7.  Regulation of Energy Homeostasis via GPR120.

Authors:  Atsuhiko Ichimura; Takafumi Hara; Akira Hirasawa
Journal:  Front Endocrinol (Lausanne)       Date:  2014-07-11       Impact factor: 5.555

Review 8.  Omega-3 Fatty Acids and FFAR4.

Authors:  Da Young Oh; Evelyn Walenta
Journal:  Front Endocrinol (Lausanne)       Date:  2014-07-16       Impact factor: 5.555

Review 9.  Treatment of type 2 diabetes by free Fatty Acid receptor agonists.

Authors:  Kenneth R Watterson; Brian D Hudson; Trond Ulven; Graeme Milligan
Journal:  Front Endocrinol (Lausanne)       Date:  2014-08-28       Impact factor: 5.555

10.  Central Agonism of GPR120 Acutely Inhibits Food Intake and Food Reward and Chronically Suppresses Anxiety-Like Behavior in Mice.

Authors:  Stéphanie Auguste; Alexandre Fisette; Maria F Fernandes; Cécile Hryhorczuk; Vincent Poitout; Thierry Alquier; Stephanie Fulton
Journal:  Int J Neuropsychopharmacol       Date:  2016-07-05       Impact factor: 5.176

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