Ginsenoside Rb1 promotes adipogenesis in 3T3-L1 cells by enhancing PPARγ2 and C/EBPα gene expression

被引:118
作者
Shang, Wenbin
Yang, Ying
Jiang, Boren
Jin, Hua
Zhou, Libin
Liu, Shangquan
Chen, Mingdao
机构
[1] Shanghai Jiao Tong Univ, Ruijin Hosp, Sch Med, Shanghai Inst Endocrine & Metab Dis, Shanghai 200025, Peoples R China
[2] Nanjing Univ Tradit Chinese Med, Coll Clin Med 1, Nanjing 210029, Peoples R China
关键词
ginsenosides Rb-1; adipogenesis; 3T3-L1; adipocytes; PPAR gamma; C/EBP alpha; proliferation; GLUT1; GLUT4;
D O I
10.1016/j.lfs.2006.10.021
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Evidence has accumulated that ginseng and its main active constituents, ginsenosides, possess anti-diabetic and insulin-sensitizing properties which may be partly realized by regulating adipocyte development and functions. In the present study, we explored the effect of ginsenoside Rb-1, the most abundant ginsenoside in ginseng root, on adipogenesis of 3T3-L1 cells. We found that with standard differentiation inducers, ginsenoside Rb-1 facilitated adipogenesis of 3T3-L1 preadipocytes in a dose-dependent manner; 10 mu M Rb-1 increased lipid accumulation by about 56%. Treatment of differentiating adipocytes with 10 mu M Rb, increased the expression of mRNA and protein of PPAR gamma(2) and C/EBP alpha, as well as mRNA of ap2, one of their target genes. After the treatment of differentiating adipocytes with Rb-1, basal and insulin-mediated glucose uptake was significantly augmented, accompanied by the up-regulation of mRNA and protein level of GLUT4, but not of GLUT1. In addition, ginsenoside Rb-1 also inhibited the proliferation of preconfluent 3T3-L1 preadipocytes. Our data indicate that anti-diabetic and insulin-sensitizing activities of ginsenosides, at least in part, are involved in the enhancing effect on PPAR-gamma(2) and C/EBP alpha expression, hence promoting adipogenesis. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:618 / 625
页数:8
相关论文
共 44 条
[21]   QUANTITATION OF ADIPOSE CONVERSION AND TRIGLYCERIDES BY STAINING INTRACYTOPLASMIC LIPIDS WITH OIL RED-O [J].
RAMIREZZACARIAS, JL ;
CASTROMUNOZLEDO, F ;
KURIHARCUCH, W .
HISTOCHEMISTRY, 1992, 97 (06) :493-497
[22]   PPARγ knockdown by engineered transcription factors:: exogenous PPARγ2 but not PPARγ1 reactivates adipogenesis [J].
Ren, DL ;
Collingwood, TN ;
Rebar, EJ ;
Wolffe, AP ;
Camp, HS .
GENES & DEVELOPMENT, 2002, 16 (01) :27-32
[23]   The transcriptional basis of adipocyte development [J].
Rosen, ED .
PROSTAGLANDINS LEUKOTRIENES AND ESSENTIAL FATTY ACIDS, 2005, 73 (01) :31-34
[24]   Molecular regulation of adipogenesis [J].
Rosen, ED ;
Spiegelman, BM .
ANNUAL REVIEW OF CELL AND DEVELOPMENTAL BIOLOGY, 2000, 16 :145-171
[25]  
Sekiya K., 1987, Phytother Res, V1, P58, DOI [10.1002/ptr.2650010203, DOI 10.1002/PTR.2650010203]
[26]   Modulating angiogenesis - The yin and the yang in ginseng [J].
Sengupta, S ;
Toh, SA ;
Sellers, LA ;
Skepper, JN ;
Koolwijk, P ;
Leung, HW ;
Yeung, HW ;
Wong, RNS ;
Sasisekharan, R ;
Fan, TPD .
CIRCULATION, 2004, 110 (10) :1219-1225
[27]  
SHEPHERD PR, 1993, J BIOL CHEM, V268, P22243
[28]   GINSENG THERAPY IN NON-INSULIN-DEPENDENT DIABETIC-PATIENTS - EFFECTS ON PSYCHOPHYSICAL PERFORMANCE, GLUCOSE HOMEOSTASIS, SERUM LIPIDS, SERUM AMINOTERMINALPROPEPTIDE CONCENTRATION, AND BODY-WEIGHT [J].
SOTANIEMI, EA ;
HAAPAKOSKI, E ;
RAUTIO, A .
DIABETES CARE, 1995, 18 (10) :1373-1375
[29]   PPAR-γ:: Adipogenic regulator and thiazolidinedione receptor [J].
Spiegelman, BM .
DIABETES, 1998, 47 (04) :507-514