Journal of Diabetes Research · 2013 · 20 citations · 6 references
MedicineEndocrinologyPharmacologyDrug DiscoveryMolecular PharmacologySignal TransductionDiabetes ControlDiabetes MellitusDiabetes PharmacotherapyG Protein-coupled Receptor SignalingGlycemic ControlPancreatic HormonesBlood Glucose RegulationDiabetes Mellitus PathophysiologyMurine ModelsOral Glucose AdministrationPancreatic Islet CellsType 2 Diabetes PharmacotherapyType 2 Diabetes Treatment
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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Kirsten Raun, Pia von Voss, C. F. Gotfredsen et al. · Diabetes · 2006 · 211 citations · Full text
Incretin agents in type 2 diabetes.
Stuart A. Ross, Jean-Marie Ékoé · PubMed · 2010 · 54 citations