ASP4000, a novel, selective, dipeptidyl peptidase 4 inhibitor with antihyperglycemic activity
Autor: | Ichiro Shima, Keiko Tanaka-Amino, Seitaro Muto, Shoji Takakura, Kazumi Matsumoto, Yoshifumi Hatakeyama |
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Rok vydání: | 2008 |
Předmět: |
Blood Glucose
Male medicine.medical_specialty medicine.medical_treatment Dipeptidyl peptidase-4 inhibitor Biology Dipeptidyl peptidase Rats Sprague-Dawley Dogs Glucagon-Like Peptide 1 In vivo Oral administration Internal medicine medicine Animals Humans Hypoglycemic Agents Insulin IC50 Dipeptidyl peptidase-4 Pharmacology Dipeptidyl-Peptidase IV Inhibitors Glucose Tolerance Test Glucagon-like peptide-1 Rats Rats Zucker Macaca fascicularis Endocrinology Azabicyclo Compounds medicine.drug |
Zdroj: | European Journal of Pharmacology. 590:444-449 |
ISSN: | 0014-2999 |
Popis: | ASP4000, (2S)-1-{[(1R,3S,4S,6R)-6-hydroxy-2-azabicyclo[2.2.1]hept-3-yl]carbonyl}-2-pyrrolidinecar bonitrile hydrochloride, is a novel dipeptidyl peptidase (DPP) 4 inhibitor. In the present study, we characterized the compound as an oral antidiabetic agent both in vitro and in vivo. ASP4000 inhibited human recombinant DPP4 with an IC50 value of 2.25 nM, and the enzyme–kinetic curve indicated that the inhibition type was competitive. In addition, ASP4000 also potently inhibited DPP4 activity in human, rat, dog, and monkey plasma at concentrations of the order of 10− 9 M, and showed high selectivity against other related enzymes, including DPP8 and DPP9. The antihyperglycemic activity of ASP4000 in vivo was examined using Zucker fa/fa rats, a type 2 diabetes animal model. A single oral administration of ASP4000 at doses of 0.03–1 mg/kg suppressed plasma DPP4 activity, and then reduced the glucose level with increasing the active GLP-1 and insulin levels in oral glucose tolerance test. These results indicate that ASP4000 is a potent, competitive, selective DPP4 inhibitor with antihyperglycemic activity, and could be a promising candidate agent for the treatment of patients with type 2 diabetes. |
Databáze: | OpenAIRE |
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