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HD047703,一种有前景的新型抗糖尿病候选药物:体内临床前研究

HD047703, a New Promising Anti-Diabetic Drug Candidate: In Vivo Preclinical Studies.

作者信息

Kim SoRa, Kim Dae Hoon, Kim Young-Seok, Ha Tae-Young, Yang Jin, Park Soo Hyun, Jeong Kwang Won, Rhee Jae-Keol

机构信息

New Drug Discovery Lab., Hyundai Pharmaceutical Co. Ltd., Gyeong-Gi Bio-Center, Suwon 443-270.

New Drug Discovery Lab., Hyundai Pharmaceutical Co. Ltd., Gyeong-Gi Bio-Center, Suwon 443-270 ; Bio-therapy Human Resources Center, Animal Medical Center and Department of Veterinary Physiology, College of Veterrinary Medicine, Chonnam National University, Gwangju 500-757.

出版信息

Biomol Ther (Seoul). 2014 Sep;22(5):400-5. doi: 10.4062/biomolther.2014.035. Epub 2014 Sep 30.

DOI:10.4062/biomolther.2014.035
PMID:25414769
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4201229/
Abstract

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.

摘要

G蛋白偶联受体119(GPR119)已成为治疗2型糖尿病的新靶点。GPR119参与胰腺β细胞和肠道细胞的葡萄糖刺激胰岛素分泌(GSIS)。在本研究中,我们鉴定了一种新型小分子GPR119激动剂HD047703,它可提高胰腺β细胞内的cAMP浓度,并有望增强人GPR119受体稳定表达细胞(CHO细胞)的葡萄糖刺激胰岛素分泌。我们通过口服葡萄糖耐量试验(OGTT)评估了HD047703在正常C57BL/6J小鼠中的急性疗效。然后,对HD047703进行长期给药,以确定其在各种糖尿病啮齿动物模型中的疗效。在正常小鼠中,单次给药HD047703可使OGTT期间的血糖控制呈剂量依赖性改善,血浆GLP-1水平也会升高。关于长期疗效,我们观察到db/db、ob/ob和DIO小鼠的血糖水平下降。这些结果表明,HD047703可能是一种有潜在前景的抗糖尿病药物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5168/4201229/1aec87bcc037/bt-22-400f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5168/4201229/40b52de84ec4/bt-22-400f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5168/4201229/8c1a7a19929d/bt-22-400f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5168/4201229/1aec87bcc037/bt-22-400f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5168/4201229/40b52de84ec4/bt-22-400f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5168/4201229/8c1a7a19929d/bt-22-400f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5168/4201229/1aec87bcc037/bt-22-400f3.jpg

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