Raloxifene promotes adipocyte differentiation of 3T3-L1 cells

被引:20
作者
Murase, Yuko
Kobayashi, Junji
Nohara, Atsushi
Asano, Akimichi
Yamaaki, Naoto
Suzuki, Kaoru
Sato, Hiroshi
Mabuchi, Hiroshi
机构
[1] Kanazawa Univ, Dept Mol Genet Cardiovasc Disorders, Grad Sch Med Sci, Kanazawa, Ishikawa 9208640, Japan
[2] Kanazawa Univ, Dept Mol Virol & Oncol, Kanazawa, Ishikawa 9208640, Japan
[3] Kanazawa Univ, Ctr Dev Mol Target Drugs, Canc Res Inst, Kanazawa, Ishikawa 9208640, Japan
关键词
raloxifene; 3T3-L1; adipocyte; adiponectin; lipoprotein lipase;
D O I
10.1016/j.ejphar.2006.03.033
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
To explore the possibility that raloxifene might influence an adipocyte differentiation and lipogenesis, we studied the effects of raloxifene on the expression of adiponectin and other peroxisome proliferator-activated receptor gamma targeting genes using the 3T3-L1 adipocytes. With standard adipogenic inducers, we added raloxifene at various doses for the adipocyte differentiation. Higher doses of raloxifene facilitated lipid accumulation of the 3T3-L1 cells. We next examined the differentiating and differentiated adipocytes and found that raloxifene augmented mRNA levels of adiponectin, adipocyte-specific fatty acid binding protein, and lipoprotein lipase dose-dependently in both. These effects were opposite those of 17 beta-estradiol treatment. These findings suggest that raloxifene promotes adipocyte differentiation, providing a novel insight into the treatment of postmenopausal metabolic syndrome with hypoadiponectinemia. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:1 / 4
页数:4
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