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Therapeutic application of GPR119 ligands in metabolic disorders

Cited 49 time in Web of Science Cited 47 time in Scopus
Authors

Yang, Jin Won; Kim, Hyo Seon; Choi, Yong-Won; Kim, Young-Mi; Kang, Keon Wook

Issue Date
2018-02
Publisher
Blackwell Publishing Inc.
Citation
Diabetes, Obesity and Metabolism, Vol.20 No.2, pp.257-269
Abstract
GPR119 belongs to the G protein-coupled receptor family and exhibits dual modes of action upon ligand-dependent activation: pancreatic secretion of insulin in a glucose-dependent manner and intestinal secretion of incretins. Hence, GPR119 has emerged as a promising target for treating type 2 diabetes mellitus without causing hypoglycaemia. However, despite continuous efforts by many major pharmaceutical companies, no synthetic GPR119 ligand has been approved as a new class of anti-diabetic agents thus far, nor has any passed beyond phase II clinical studies. Herein, we summarize recent advances in research concerning the physiological/pharmacological effects of GPR119 and its synthetic ligands on the regulation of energy metabolism, and we speculate on future applications of GPR119 ligands for the treatment of metabolic diseases, focusing on non-alcoholic fatty liver disease.
ISSN
1462-8902
Language
English
URI
https://hdl.handle.net/10371/149832
DOI
https://doi.org/10.1111/dom.13062
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