Effect of Ginsenosides Rg3 and Re on Glucose Transport in Mature 3T3-L1 Adipocytes

被引:54
作者
Lee, Ok-Hwan [1 ]
Lee, Hee-Hyun [2 ]
Kim, Ji-Hyup [2 ]
Lee, Boo-Yong [2 ]
机构
[1] Kangwon Natl Univ, Dept Food Sci & Biotechnol, Chunchon 200701, South Korea
[2] CHA Univ, Dept Biomed Sci, Kyonggi Do 463836, South Korea
关键词
ginsenoside Rg3 and Re; mature; 3T3-L1; cells; glucose uptake; PI3K pathway; IRS-1; GLUT4; INSULIN; ACTIVATION; MUSCLE; CELLS;
D O I
10.1002/ptr.3322
中图分类号
R914 [药物化学];
学科分类号
100705 [微生物与生化药学];
摘要
Ginsenosides, the active component of Panax ginseng, have been shown to evidence a variety of biological activities associated with hyperglycemia, obesity and type 2 diabetes mellitus. This study evaluated the effects of the ginsenosides, Rg3 and Re, on glucose uptake and the glucose transport system in mature 3T3-L1 cells. The results demonstrated that the glucose uptake of ginsenosides Rg3 and Re at concentrations of 1-10 mu M significantly increased by approximately similar to 10% and similar to 12%, respectively. Furthermore, the glucose transporter 4 (GLUT4) mRNA expression of ginsenosides Rg3 and Re at 10 mu M was increased by approximately similar to 1.73 and 1.43 fold, respectively. It was further confirmed in a series of experiments that ginsenosides Rg3 and Re stimulated the mRNA expression of insulin receptor substrate (IRS-1) and the expression of phosphatidylinositol 3-kinase (PI3K)-110 alpha protein, which is involved in downstream events in the insulin signaling pathway. These findings demonstrate that ginsenosides Rg3 and Re may stimulate glucose uptake via the PI3K pathways involving IRS-1. Further, our results suggest that both of these ginsenosides might prove useful as effective antidiabetic and antihyperglycemic agents. Copyright (C) 2010 John Wiley & Sons, Ltd.
引用
收藏
页码:768 / 773
页数:6
相关论文
共 18 条
[1]
Antidiabetic effects of Panax ginseng berry extract and the identification of an effective component [J].
Attele, AS ;
Zhou, YP ;
Xie, JT ;
Wu, JA ;
Zhang, L ;
Dey, L ;
Pugh, W ;
Rue, PA ;
Polonsky, KS ;
Yuan, CS .
DIABETES, 2002, 51 (06) :1851-1858
[2]
Ginseng pharmacology - Multiple constituents and multiple actions [J].
Attele, AS ;
Wu, JA ;
Yuan, CS .
BIOCHEMICAL PHARMACOLOGY, 1999, 58 (11) :1685-1693
[3]
Carvalho Eugenia, 2001, FASEB Journal, V15, P1101
[4]
Ginsenoside, Re of Panax ginseng possesses significant antioxidant and antihyperlipidemic efficacies in streptozotocin-induced diabetic rats [J].
Cho, William C. S. ;
Chung, Wai-Shing ;
Lee, Sally K. W. ;
Leung, Albert W. N. ;
Cheng, Christopher H. K. ;
Yue, Kevin K. M. .
EUROPEAN JOURNAL OF PHARMACOLOGY, 2006, 550 (1-3) :173-179
[5]
THE HUMAN INSULIN-RECEPTOR CDNA - THE STRUCTURAL BASIS FOR HORMONE-ACTIVATED TRANSMEMBRANE SIGNALING [J].
EBINA, Y ;
ELLIS, L ;
JARNAGIN, K ;
EDERY, M ;
GRAF, L ;
CLAUSER, E ;
OU, JH ;
MASIARZ, F ;
KAN, YW ;
GOLDFINE, ID ;
ROTH, RA ;
RUTTER, WJ .
CELL, 1985, 40 (04) :747-758
[6]
ELMENDORF JS, 1995, BIOCHEM BIOPH RES CO, V28, P1147
[7]
Impaired glucose transport and insulin receptor tyrosine phosphorylation in skeletal muscle from obese women with gestational diabetes [J].
Friedman, JE ;
Ishizuka, T ;
Shao, JH ;
Huston, L ;
Highman, T ;
Catalano, P .
DIABETES, 1999, 48 (09) :1807-1814
[8]
Activation of the glucose transporter GLUT4 by insulin [J].
Furtado, LM ;
Somwar, R ;
Sweeney, G ;
Niu, WY ;
Klip, A .
BIOCHEMISTRY AND CELL BIOLOGY, 2002, 80 (05) :569-578
[9]
SUBLINES OF MOUSE 3T3 CELLS THAT ACCUMULATE LIPID [J].
GREEN, H ;
KEHINDE, O .
CELL, 1974, 1 (03) :113-116
[10]
Helms Steve, 2004, Altern Med Rev, V9, P259