Antidiabetic effect of a novel non-thiazolidinedione PPAR γ/α agonist on ob/ob mice

被引:17
|
作者
Hu, Xi [1 ]
Feng, Ying [1 ]
Shen, Yu [1 ]
Zhao, Xiao-feng [1 ]
Yu, Juan-hong [1 ]
Yang, Yu-she [1 ]
Leng, Ying [1 ]
机构
[1] Chinese Acad Sci, Shanghai Inst Biol Sci, Shanghai Inst Mat Med, Shanghai 201203, Peoples R China
关键词
diabetes; insulin-sensitizing; peroxisome proliferator-activated receptors; thiazolidinediones;
D O I
10.1111/j.1745-7254.2006.00427.x
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Aim: To study whether T33, a new synthesized non-thiazolidinedione (TZD) peroxisome proliferator-activated receptor (PPAR) gamma/alpha dual agonist has an antidiabetic effect on ob/ob mice. Methods: Ob/ob mice were treated with 4 mg/kg or 8 mg/kg T33 by gavage for 20 d. Blood glucose levels were measured regularly. An oral glucose tolerance test (OGTT) and an insulin tolerance test (ITT) were preformed on d 8 and d 12, respectively. The levels of insulin, triglyceride and free fatty acid (FFA) in the serum were measured at the end of administration. The intramuscular and liver triglyceride content was also determined. Results: T33 reduced the hyperglycemia, hyperinsulinemia and hyperlipidemia of the ob/ob mice. The OGTT and ITT showed that the insulin resistance state of the ob/ob mice was obviously ameliorated after T33 treatment. After 20 d treatment with 8 mg/kg T33, the triglyceride content in the gastrocnemius muscle decreased significantly. T33 did not have any effect on triglyceride content in the liver, whereas rosiglitazone significantly increased the hepatocyte lipid deposition. Conclusion: The PPAR gamma/alpha dual agonist T33 has antidiabetic and insulin-sensitizing effects in ob/ob mice. It has the potential to be a new therapeutic candidate for the treatment of type 2 diabetes.
引用
收藏
页码:1346 / 1352
页数:7
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