Effect of Ganoderma applanatum Mycelium Extract on the Inhibition of Adipogenesis in 3T3-L1 Adipocytes

被引:8
|
作者
Kim, Ji-Eun [1 ]
Park, Sung-Jin [1 ]
Yu, Mi-Hee [1 ]
Lee, Sam-Pin [1 ]
机构
[1] Keimyung Univ, Dept Food Sci & Technol, Taegu 704701, South Korea
基金
新加坡国家研究基金会;
关键词
GPDH activity; anti-obesity; 3T3-L1; cell; Ganoderma applanatum; PPAR gamma; DOWN-REGULATION; ACID; EXOPOLYSACCHARIDES; DIFFERENTIATION; PPAR-GAMMA-2; SUPPRESS; CULTURE; WEIGHT; TEA;
D O I
10.1089/jmf.2013.3036
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Ganoderma applanatum (GA) and related fungal species have been used for over 2000 years in China to prevent and treat various human diseases. However, there is no critical research evaluating the functionality of GA grown using submerged culture technology. This study aimed to evaluate the effects of submerged culture GA mycelium (GAM) and its active components (protocatechualdehyde [PCA]) on preadipocyte differentiation of 3T3-L1 cells. Mouse-derived preadipocyte 3T3-L1 cells were treated with differentiation inducers in the presence or absence of GAM extracts. We determined triglyceride accumulations, glycerol-3-phosphate dehydrogenase (GPDH) activities, and differentiation makers. PCA, the active component of GAM extract, was also used to treat 3T3-L1 cells. The MTT assay showed that the GAM extract (0.01-1 mg/mL) was not toxic to 3T3-L1 preadipocyte. Treatment of cells with GAM extracts and its active components significantly decreased the GPDH activity and lipid accumulation, a marker of adipogenesis, in a dose-dependent manner. Western blot analysis results showed that the protein expression levels of peroxisome proliferator-activated receptor gamma (PPAR gamma), CCAAT/enhancer-binding protein alpha (C/EBP alpha), and sterol regulatory element-binding protein 1 (SREBP1) were inhibited by the GAM extract. In addition, adipogenic-specific genes such as perilipin, fatty acid synthase (FAS), fatty acid transport protein 1 (FATP1), and fatty acid-binding protein 4 (FABP4) decreased in a dose-dependent manner. Quantitative high-performance liquid chromatography analysis showed that the GAM extract contained 1.14 mg/g PCA. GAM extracts suppressed differentiation of 3T3-L1 preadipocytes, in part, through altered regulation of PPAR gamma, C/EBP alpha, and SREBP1. These results suggest that GAM extracts and PCA may suppress adipogenesis by inhibiting differentiation of preadipocytes.
引用
收藏
页码:1086 / 1094
页数:9
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