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In Vivo Efficacy of HD0471953: A Novel GPR119 Agonist for the Treatment of Type 2 Diabetes Mellitus

G-protein coupled receptor 119 (GPR119) has emerged as a promising new target for the treatment of type 2 diabetes mellitus. The expression of GPR119 on the pancreatic B cells and intestinal L cells provides a unique opportunity for a single drug to promote insulin and GLP-1 secretion. In this study...

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Autores principales: Kim, So Ra, Kim, Dae-Hoon, Park, Soo Hyun, Kim, Young Seok, Kim, Chun Hwa, Ha, Tae-Young, Yang, Jin, Rhee, Jae-Keol
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3872231/
https://www.ncbi.nlm.nih.gov/pubmed/24386644
http://dx.doi.org/10.1155/2013/269569
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author Kim, So Ra
Kim, Dae-Hoon
Park, Soo Hyun
Kim, Young Seok
Kim, Chun Hwa
Ha, Tae-Young
Yang, Jin
Rhee, Jae-Keol
author_facet Kim, So Ra
Kim, Dae-Hoon
Park, Soo Hyun
Kim, Young Seok
Kim, Chun Hwa
Ha, Tae-Young
Yang, Jin
Rhee, Jae-Keol
author_sort Kim, So Ra
collection PubMed
description G-protein coupled receptor 119 (GPR119) has emerged as a promising new target for the treatment of type 2 diabetes mellitus. The expression of GPR119 on the pancreatic B cells and intestinal L cells provides a unique opportunity for a single drug to promote insulin and GLP-1 secretion. In this study, we identified a novel small molecule GPR119 agonist, HD0471953, from our large library of synthetic compounds based on its ability to anti-hyperglycemic effects on T2DM murine models. We have tested the acute efficacy of HD0471953 by the oral glucose tolerance test (OGTT) with normal C57BL/6J mice. Then, chronic administrations of HD0471953 were performed to evaluate the efficacy on various diabetic rodent models. Single administration of HD0471953 showed improved glycemic control with a dose-dependent manner in OGTT with normal mice, and the insulin and GLP-1 were also increased. To identify chronic efficacy, we have observed a decline of blood glucose and fasting insulin in a dose-dependent manner of 10, 20, and 50 mpk in db/db mice. The results suggest that HD0471953 may be a potentially promising anti-hyperglycemic agent for the treatment of patients with type 2 diabetes mellitus.
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spelling pubmed-38722312014-01-02 In Vivo Efficacy of HD0471953: A Novel GPR119 Agonist for the Treatment of Type 2 Diabetes Mellitus Kim, So Ra Kim, Dae-Hoon Park, Soo Hyun Kim, Young Seok Kim, Chun Hwa Ha, Tae-Young Yang, Jin Rhee, Jae-Keol J Diabetes Res Research Article G-protein coupled receptor 119 (GPR119) has emerged as a promising new target for the treatment of type 2 diabetes mellitus. The expression of GPR119 on the pancreatic B cells and intestinal L cells provides a unique opportunity for a single drug to promote insulin and GLP-1 secretion. In this study, we identified a novel small molecule GPR119 agonist, HD0471953, from our large library of synthetic compounds based on its ability to anti-hyperglycemic effects on T2DM murine models. We have tested the acute efficacy of HD0471953 by the oral glucose tolerance test (OGTT) with normal C57BL/6J mice. Then, chronic administrations of HD0471953 were performed to evaluate the efficacy on various diabetic rodent models. Single administration of HD0471953 showed improved glycemic control with a dose-dependent manner in OGTT with normal mice, and the insulin and GLP-1 were also increased. To identify chronic efficacy, we have observed a decline of blood glucose and fasting insulin in a dose-dependent manner of 10, 20, and 50 mpk in db/db mice. The results suggest that HD0471953 may be a potentially promising anti-hyperglycemic agent for the treatment of patients with type 2 diabetes mellitus. Hindawi Publishing Corporation 2013 2013-12-12 /pmc/articles/PMC3872231/ /pubmed/24386644 http://dx.doi.org/10.1155/2013/269569 Text en Copyright © 2013 So Ra Kim et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Kim, So Ra
Kim, Dae-Hoon
Park, Soo Hyun
Kim, Young Seok
Kim, Chun Hwa
Ha, Tae-Young
Yang, Jin
Rhee, Jae-Keol
In Vivo Efficacy of HD0471953: A Novel GPR119 Agonist for the Treatment of Type 2 Diabetes Mellitus
title In Vivo Efficacy of HD0471953: A Novel GPR119 Agonist for the Treatment of Type 2 Diabetes Mellitus
title_full In Vivo Efficacy of HD0471953: A Novel GPR119 Agonist for the Treatment of Type 2 Diabetes Mellitus
title_fullStr In Vivo Efficacy of HD0471953: A Novel GPR119 Agonist for the Treatment of Type 2 Diabetes Mellitus
title_full_unstemmed In Vivo Efficacy of HD0471953: A Novel GPR119 Agonist for the Treatment of Type 2 Diabetes Mellitus
title_short In Vivo Efficacy of HD0471953: A Novel GPR119 Agonist for the Treatment of Type 2 Diabetes Mellitus
title_sort in vivo efficacy of hd0471953: a novel gpr119 agonist for the treatment of type 2 diabetes mellitus
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3872231/
https://www.ncbi.nlm.nih.gov/pubmed/24386644
http://dx.doi.org/10.1155/2013/269569
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