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HD047703, a New Promising Anti-Diabetic Drug Candidate: In Vivo Preclinical Studies
G-protein coupled receptor 119 (GPR119) has emerged as a novel target for the treatment of type 2 diabetes mellitus. GPR119 is involved in glucose-stimulated insulin secretion (GSIS) from the pancreatic β-cells and intestinal cells. In this study, we identified a novel small-molecule GPR119 agonist,...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Korean Society of Applied Pharmacology
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4201229/ https://www.ncbi.nlm.nih.gov/pubmed/25414769 http://dx.doi.org/10.4062/biomolther.2014.035 |
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author | Kim, SoRa Kim, Dae Hoon Kim, Young-Seok Ha, Tae-Young Yang, Jin Park, Soo Hyun Jeong, Kwang Won Rhee, Jae-Keol |
author_facet | Kim, SoRa Kim, Dae Hoon Kim, Young-Seok Ha, Tae-Young Yang, Jin Park, Soo Hyun Jeong, Kwang Won Rhee, Jae-Keol |
author_sort | Kim, SoRa |
collection | PubMed |
description | G-protein coupled receptor 119 (GPR119) has emerged as a novel target for the treatment of type 2 diabetes mellitus. GPR119 is involved in glucose-stimulated insulin secretion (GSIS) from the pancreatic β-cells and intestinal cells. In this study, we identified a novel small-molecule GPR119 agonist, HD047703, which raises intracellular cAMP concentrations in pancreatic β-cells and can be expected to potentiate glucose-stimulated insulin secretion from human GPR119 receptor stably expressing cells (CHO cells). We evaluated the acute efficacy of HD047703 by the oral glucose tolerance test (OGTT) in normal C57BL/6J mice. Then, chronic administrations of HD047703 were performed to determine its efficacy in various diabetic rodent models. Single administration of HD047703 caused improved glycemic control during OGTT in a dose-dependent manner in normal mice, and the plasma GLP-1 level was also increased. With respect to chronic efficacy, we observed a decline in blood glucose levels in db/db, ob/ob and DIO mice. These results suggest that HD047703 may be a potentially promising anti-diabetic agent. |
format | Online Article Text |
id | pubmed-4201229 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | The Korean Society of Applied Pharmacology |
record_format | MEDLINE/PubMed |
spelling | pubmed-42012292014-11-20 HD047703, a New Promising Anti-Diabetic Drug Candidate: In Vivo Preclinical Studies Kim, SoRa Kim, Dae Hoon Kim, Young-Seok Ha, Tae-Young Yang, Jin Park, Soo Hyun Jeong, Kwang Won Rhee, Jae-Keol Biomol Ther (Seoul) Original Article G-protein coupled receptor 119 (GPR119) has emerged as a novel target for the treatment of type 2 diabetes mellitus. GPR119 is involved in glucose-stimulated insulin secretion (GSIS) from the pancreatic β-cells and intestinal cells. In this study, we identified a novel small-molecule GPR119 agonist, HD047703, which raises intracellular cAMP concentrations in pancreatic β-cells and can be expected to potentiate glucose-stimulated insulin secretion from human GPR119 receptor stably expressing cells (CHO cells). We evaluated the acute efficacy of HD047703 by the oral glucose tolerance test (OGTT) in normal C57BL/6J mice. Then, chronic administrations of HD047703 were performed to determine its efficacy in various diabetic rodent models. Single administration of HD047703 caused improved glycemic control during OGTT in a dose-dependent manner in normal mice, and the plasma GLP-1 level was also increased. With respect to chronic efficacy, we observed a decline in blood glucose levels in db/db, ob/ob and DIO mice. These results suggest that HD047703 may be a potentially promising anti-diabetic agent. The Korean Society of Applied Pharmacology 2014-09-30 2014-09 /pmc/articles/PMC4201229/ /pubmed/25414769 http://dx.doi.org/10.4062/biomolther.2014.035 Text en Copyright ©2014, The Korean Society of Applied Pharmacology http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Kim, SoRa Kim, Dae Hoon Kim, Young-Seok Ha, Tae-Young Yang, Jin Park, Soo Hyun Jeong, Kwang Won Rhee, Jae-Keol HD047703, a New Promising Anti-Diabetic Drug Candidate: In Vivo Preclinical Studies |
title | HD047703, a New Promising Anti-Diabetic Drug Candidate: In Vivo Preclinical Studies |
title_full | HD047703, a New Promising Anti-Diabetic Drug Candidate: In Vivo Preclinical Studies |
title_fullStr | HD047703, a New Promising Anti-Diabetic Drug Candidate: In Vivo Preclinical Studies |
title_full_unstemmed | HD047703, a New Promising Anti-Diabetic Drug Candidate: In Vivo Preclinical Studies |
title_short | HD047703, a New Promising Anti-Diabetic Drug Candidate: In Vivo Preclinical Studies |
title_sort | hd047703, a new promising anti-diabetic drug candidate: in vivo preclinical studies |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4201229/ https://www.ncbi.nlm.nih.gov/pubmed/25414769 http://dx.doi.org/10.4062/biomolther.2014.035 |
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