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Pharmacological Profile of NCP-322, a Novel G Protein-Coupled Receptor 119 Agonist, as an Orally Active Therapeutic Agent for Type 2 Diabetes Mellitus.
- Source :
-
Biological & pharmaceutical bulletin [Biol Pharm Bull] 2025; Vol. 48 (1), pp. 65-74. - Publication Year :
- 2025
-
Abstract
- Pharmacological activation of G protein-coupled receptor 119 (GPR119) produces pleiotropic beneficial effects, including the promotion of insulin secretion from pancreatic β-cells, enhancement of glucagon-like peptide (GLP)-1 secretion from intestinal L cells, glucose-dependent insulin secretion, and food intake and body weight gain suppression. Thus, GPR119 has attracted attention as a promising new target for type 2 diabetes mellitus (T2DM) treatment. Here, we identified a new small GPR119 agonist, NCP-322. This compound showed potent enhancing effects on insulin and GLP-1 secretion, which played a role in pancreatic β-cells and intestinal L cells. In the oral glucose tolerance test, NCP-322 administration reduced glycemic excursions that were only exhibited during hyperglycemia. Furthermore, NCP-322 administration did not induce hypoglycemia, the main side effect of antidiabetic drugs. These results suggest the promising therapeutic potential of NCP-322 for T2DM treatment.
- Subjects :
- Animals
Male
Glucose Tolerance Test
Blood Glucose drug effects
Humans
Insulin-Secreting Cells drug effects
Insulin-Secreting Cells metabolism
Administration, Oral
Mice
Insulin Secretion drug effects
Receptors, G-Protein-Coupled agonists
Receptors, G-Protein-Coupled metabolism
Diabetes Mellitus, Type 2 drug therapy
Diabetes Mellitus, Type 2 metabolism
Hypoglycemic Agents pharmacology
Hypoglycemic Agents therapeutic use
Hypoglycemic Agents administration & dosage
Insulin
Glucagon-Like Peptide 1 agonists
Subjects
Details
- Language :
- English
- ISSN :
- 1347-5215
- Volume :
- 48
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- Biological & pharmaceutical bulletin
- Publication Type :
- Academic Journal
- Accession number :
- 39894557
- Full Text :
- https://doi.org/10.1248/bpb.b24-00737