Literature DB >> 23442069

Is GPR119 agonism an appropriate treatment modality for the safe amelioration of metabolic diseases?

Lauren M Cornall1, Michael L Mathai, Deanne H Hryciw, Andrew J McAinch.   

Abstract

INTRODUCTION: GPR119 is a recently deorphanised G-protein coupled receptor which has been suggested to be important in mediating systemic metabolic homeostasis. Research to date has primarily focused on the ability of GPR119 to promote euglycaemia and thus as a therapeutic target for the treatment of type 2 diabetes mellitus (T2DM). Indeed, previous studies have shown that GPR119 promotes glucose-stimulated insulin secretion, pancreatic β-cell function and glucagon-like peptide-1 release, all of which provide valid mechanisms through which GPR119 may improve systemic glucose homeostasis. AREAS COVERED: In the current review, the authors provide a brief overview of the known functions of GPR119 and then discuss the novel potential for GPR119 to regulate metabolic function in skeletal and cardiac muscle and how this may translate to improvements or impairments in systemic health. EXPERT OPINION: GPR119 is largely purported as being anti-diabetic and has been rapidly progressed to clinical trials, mainly as anti-diabetic agents. However, emerging data suggest that this class of agonists may have a detrimental effect at the level of the muscle. This may potentiate the development and progression of metabolic diseases such as T2DM. Therefore, further research is required before GPR119 receptor agonists can be prescribed with confidence as an anti-diabetic agent.

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Year:  2013        PMID: 23442069     DOI: 10.1517/13543784.2013.775245

Source DB:  PubMed          Journal:  Expert Opin Investig Drugs        ISSN: 1354-3784            Impact factor:   6.206


  5 in total

1.  Gastrointestinal hormonal responses on GPR119 activation in lean and diseased rodent models of type 2 diabetes.

Authors:  S Patel; O J Mace; I R Tough; J White; T-A Cock; U Warpman Berglund; M Schindler; H M Cox
Journal:  Int J Obes (Lond)       Date:  2014-01-23       Impact factor: 5.095

2.  Molecular matchmaking between the popular weight-loss herb Hoodia gordonii and GPR119, a potential drug target for metabolic disorder.

Authors:  Shuyong Zhang; Yuyong Ma; Jing Li; Junjun Ma; Biao Yu; Xin Xie
Journal:  Proc Natl Acad Sci U S A       Date:  2014-09-22       Impact factor: 11.205

3.  Lipid derivatives activate GPR119 and trigger GLP-1 secretion in primary murine L-cells.

Authors:  Catherine E Moss; Leslie L Glass; Eleftheria Diakogiannaki; Ramona Pais; Carol Lenaghan; David M Smith; Marianne Wedin; Mohammad Bohlooly-Y; Fiona M Gribble; Frank Reimann
Journal:  Peptides       Date:  2015-07-02       Impact factor: 3.750

Review 4.  Targeting the GPR119/incretin axis: a promising new therapy for metabolic-associated fatty liver disease.

Authors:  Jianan Zhao; Yu Zhao; Yiyang Hu; Jinghua Peng
Journal:  Cell Mol Biol Lett       Date:  2021-07-07       Impact factor: 5.787

5.  Bidirectional GPR119 Agonism Requires Peptide YY and Glucose for Activity in Mouse and Human Colon Mucosa.

Authors:  Iain R Tough; Sarah Forbes; Herbert Herzog; Robert M Jones; Thue W Schwartz; Helen M Cox
Journal:  Endocrinology       Date:  2018-04-01       Impact factor: 4.736

  5 in total

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