Artepillin C, as a PPARγ ligand, enhances adipocyte differentiation and glucose uptake in 3T3-L1 cells

被引:70
作者
Choi, Sun-Sil [2 ]
Cha, Byung-Yoon [2 ]
Iida, Kagami [2 ]
Lee, Young-Sil [2 ]
Yonezawa, Takayuki [2 ]
Teruya, Toshiaki [2 ]
Nagai, Kazuo [1 ,2 ]
Woo, Je-Tae [1 ,2 ,3 ]
机构
[1] Chubu Univ, Dept Biol Chem, Aichi 4878501, Japan
[2] Chubu Univ, Res Inst Biol Funct, Aichi 4878501, Japan
[3] Erina Co Inc, Dept Res & Dev, Minato Ku, Tokyo 1050021, Japan
关键词
Artepillin C; 3T3-L1; cells; Adipocyte differentiation; PPAR gamma ligand; Glucose uptake; NECROSIS-FACTOR-ALPHA; BRAZILIAN PROPOLIS; ADIPOSE-TISSUE; INSULIN STIMULATION; GENE-EXPRESSION; TRANSGENIC MICE; PLANT-ORIGIN; TRANSPORT; ACTIVATION; GLUCOSE-TRANSPORTER-4;
D O I
10.1016/j.bcp.2011.01.002
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The nuclear receptor peroxisome proliferator-activated receptor (PPAR) gamma plays an important role in adipocyte differentiation. Its ligands, including thiazolidinediones, improve insulin sensitivity in type 2 diabetes. We investigated the effects of artepillin C, an ingredient of Baccharis dracunculifolia, on adipogenesis and glucose uptake using 3T3-L1 cells. In PPAR gamma ligand-binding assays, artepillin C exhibited binding affinity toward PPAR gamma. Artepillin C dose-dependently enhanced adipocyte differentiation of 3T3-L1 cells. As a result of the artepillin C-induced adipocyte differentiation, the gene expression of PPAR gamma and its target genes, such as aP2, adiponectin and glucose transporter (GLUT) 4, was increased. These increases were abolished by cotreatment with GW9662, a PPAR gamma antagonist. In mature 3T3-L1 adipocytes, artepillin C significantly enhanced the basal and insulin-stimulated glucose uptake. These effects were decreased by cotreatment with a PI3K inhibitor. Although artepillin C had no effects on the insulin signaling cascade, artepillin C enhanced the expression and plasma membrane translocation of GLUT1 and GLUT4 in mature adipocytes. In conclusion, these findings suggest that artepillin C promotes adipocyte differentiation and glucose uptake in part by direct binding to PPAR gamma, which could be the basis of the pharmacological benefits of green propolis intake in reducing the risk of type 2 diabetes. (C) 2011 Elsevier Inc. All rights reserved.
引用
收藏
页码:925 / 933
页数:9
相关论文
共 52 条
[1]   ISOLATION AND IDENTIFICATION OF ANTIMICROBIAL COMPOUNDS IN BRAZILIAN PROPOLIS [J].
AGA, H ;
SHIBUYA, T ;
SUGIMOTO, T ;
KURIMOTO, M ;
NAKAJIMA, S .
BIOSCIENCE BIOTECHNOLOGY AND BIOCHEMISTRY, 1994, 58 (05) :945-946
[2]  
[Anonymous], FEBS LETT
[3]   Effects of adenoviral gene transfer of wild-type, constitutively active, and kinase-defective protein kinase C-λ on insulin-stimulated glucose transport in L6 myotubes [J].
Bandyopadhyay, G ;
Kanoh, Y ;
Sajan, MP ;
Standaert, ML ;
Farese, RV .
ENDOCRINOLOGY, 2000, 141 (11) :4120-4127
[4]  
Bandyopadhyay G, 1997, J BIOL CHEM, V272, P2551
[5]   Evidence for involvement of protein kinase C (PKC)-zeta and noninvolvement of diacylglycerol-sensitive PKCs in insulin-stimulated glucose transport in L6 myotubes [J].
Bandyopadhyay, G ;
Standaert, ML ;
Galloway, L ;
Moscat, J ;
Farese, RV .
ENDOCRINOLOGY, 1997, 138 (11) :4721-4731
[6]  
Bankova V, 1999, Z NATURFORSCH C, V54, P401
[7]   Novel peroxisome proliferator-activated receptor (PPAR) γ and PPARδ ligands produce distinct biological effects [J].
Berger, J ;
Leibowitz, MD ;
Doebber, TW ;
Elbrecht, A ;
Zhang, B ;
Zhou, GC ;
Biswas, C ;
Cullinan, CA ;
Hayes, NS ;
Li, Y ;
Tanen, M ;
Ventre, J ;
Wu, MS ;
Berger, GD ;
Mosley, R ;
Marquis, R ;
Santini, C ;
Sahoo, SP ;
Tolman, RL ;
Smith, RG ;
Moller, DE .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (10) :6718-6725
[8]   PPAR gamma and the molecular control of adipogenesis [J].
Brun, RP ;
Spiegelman, BM .
JOURNAL OF ENDOCRINOLOGY, 1997, 155 (02) :217-218
[9]  
CALDERHEAD DM, 1990, J BIOL CHEM, V265, P13800
[10]   Magnolol enhances adipocyte differentiation and glucose uptake in 3T3-L1 cells [J].
Choi, Sun-Sil ;
Cha, Byung-Yoon ;
Lee, Young-Sil ;
Yonezawa, Takayuki ;
Teruya, Toshiaki ;
Nagai, Kazuo ;
Woo, Je-Tae .
LIFE SCIENCES, 2009, 84 (25-26) :908-914