Hypoglycemic Activity and the Potential Mechanism of the Flavonoid Rich Extract from Sophora tonkinensis Gagnep. in KK-Ay Mice

被引:44
作者
Huang, Mi [1 ]
Deng, Shihao [1 ]
Han, Qianqian [1 ]
Zhao, Ping [1 ]
Zhou, Qi [1 ]
Zheng, Sijian [1 ]
Ma, Xinhua [1 ]
Xu, Chan [1 ]
Yang, Jing [1 ]
Yang, Xinzhou [1 ,2 ,3 ]
机构
[1] South Cent Univ Nationalities, Sch Pharmaceut Sci, Wuhan, Peoples R China
[2] Chinese Acad Sci, Shanghai Inst Mat Med, State Key Lab Drug Res, Shanghai, Peoples R China
[3] Tianjin Univ Sci & Technol, Coll Biol Engn, Tianjin, Peoples R China
基金
中国国家自然科学基金;
关键词
hypoglycemic agents; Sophora tonkinensis Gagnep; KK-Ay mice; GLUT4; p-AMPK; PRENYLATED FLAVONOIDS; GLUCOSE; GLUT4; CELL; CONSTITUENTS; DYSFUNCTION; LEAVES;
D O I
10.3389/fphar.2016.00288
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
This study investigated the active principles, hypoglycemic activity and potential mechanisms of the flavonoid rich extract from Sophora tonkinensis Gagnep. (ST-EtOAc) in KK-Ay diabetic mice. An off-line semipreparative liquid chromatography-nuclear magnetic resonance (LC-NMR) and liquid chromatography-ultraviolet-electrospray ionization mass spectrometry (LC-UV-ESIMS) protocol was performed to determine 13 flavonoids from ST-EtOAc. ST-EtOAc administrated orally to the KK-Ay mice significantly increased their sensibility to insulin, reduced fasting blood-glucose levels and blood lipid indexes such as triglyceride and cholesterol. Moreover, ST-EtOAc exhibited a strong effect of stimulation on glucose transporter 4 (GLUT4) translocation by 2.7-fold in L6 cells. However, the selective AMP-activated protein kinase (AMPK) inhibitor compound C can completely inhibit the activation of the AMPK pathway and prevent the GLUT4 translocation caused by ST-EtOAc. In vivo, phosphorylation of the AMPK expression in the liver and skeletal muscle was measured. The results showed phosphorylation of the AMPK had been improved and GLUT4 expression had been also enhanced. In this paper, we conclude that, ST-EtOAc seems to have potential beneficial effects on the treatment of type 2 diabetes mellitus with the probable mechanism of stimulating GLUT4 translocation modulated by the AMPK pathway.
引用
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页数:12
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