| RRC ID |
43402
|
| 著者 |
Fujimori Y, Katsuno K, Nakashima I, Ishikawa-Takemura Y, Fujikura H, Isaji M.
|
| タイトル |
Remogliflozin etabonate, in a novel category of selective low-affinity sodium glucose cotransporter (SGLT2) inhibitors, exhibits antidiabetic efficacy in rodent models.
|
| ジャーナル |
J Pharmacol Exp Ther
|
| Abstract |
The low-affinity sodium glucose cotransporter (SGLT2) plays an important role in renal glucose reabsorption and is a remarkable transporter as a molecular target for the treatment of diabetes. We have discovered remogliflozin etabonate, which is a novel category of selective SGLT2 inhibitors. Remogliflozin etabonate is a prodrug based on benzylpyrazole glucoside and is metabolized to its active form, remogliflozin, in the body. We identified remogliflozin to be a potent and highly selective SGLT2 inhibitor by examining COS-7 cells transiently expressing either high-affinity sodium glucose cotransporter (SGLT1) or SGLT2. Orally administered remogliflozin etabonate increased urinary glucose excretion in a dose-dependent manner in both mice and rats. By increasing urinary glucose excretion, remogliflozin etabonate inhibited the increase in plasma glucose after glucose loading without stimulating insulin secretion in normal rats. Remogliflozin etabonate also showed antihyperglycemic effects in both streptozotocin-induced diabetic rats in oral glucose tolerance and in db/db mice in the fed condition. Chronic treatment with remogliflozin etabonate reduced the levels of fasting plasma glucose and glycated hemoglobin, and it ameliorated glucosuria in db/db mice. In high-fat diet-fed Goto-Kakizaki rats, remogliflozin etabonate improved hyperglycemia, hyperinsulinemia, hypertriglyceridemia, and insulin resistance. This study demonstrates that treatment with remogliflozin etabonate exhibits antidiabetic efficacy in several rodent models and suggests that remogliflozin etabonate may be a new and useful drug for the treatment of diabetes.
|
| 巻・号 |
327(1)
|
| ページ |
268-76
|
| 公開日 |
2008-10-1
|
| DOI |
10.1124/jpet.108.140210
|
| PII |
jpet.108.140210
|
| PMID |
18583547
|
| MeSH |
Animals
COS Cells
Chlorocebus aethiops
Disease Models, Animal
Dose-Response Relationship, Drug
Female
Glucose Tolerance Test
Glucosides / pharmacology*
Glycosuria / chemically induced
Humans
Hypoglycemic Agents / pharmacology*
Insulin Resistance
Male
Mice
Mice, Inbred C57BL
Pyrazoles / pharmacology*
Rats
Rats, Sprague-Dawley
Rats, Wistar
Sodium-Glucose Transporter 2
Sodium-Glucose Transporter 2 Inhibitors*
|
| IF |
3.561
|
| 引用数 |
166
|
|
WOS 分野
|
PHARMACOLOGY & PHARMACY
|
| リソース情報 |
| ヒト・動物細胞 |
|
