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KMID : 1129720140310040168
Korean Journal of Acupuncture
2014 Volume.31 No. 4 p.168 ~ p.178
Effects of Mahuang-Chuanwu(Mahwang-Cheonoh) Pharmacopuncture Solution on Adipocyte Differentiation and Gene Expression in 3T3-L1 Adipocytes
°­°æÈ­:Kang Kyung-Hwa
ÀúÀÚ¾øÀ½:No authors listed
Abstract
Objectives : Mahuang-Chuanwu(Mahwang-Cheonoh) Pharmacopuncture(MCP) has been used to treat obesity in Clinical Korean Medicine. MCP solution(MCPS) is also expected to have strong anti-obesity activities. However, little is known about the mechanisms of its inhibitory effects on adipocyte differentiation and lipogenesis.

Methods : In the present study, we examined the effects of MCPS on differentiation and lipogenesis of 3T3-L1 adipocytes. To elucidate the mechanism of the effects of MCPS on lowering lipid content in 3T3-L1 adipocytes, we examined whether MCPS modulates the expressions of transcription factors to induce lipogenesis and adipogenic genes related to regulate the accumulation of lipids.

Results : Our results showed that MCPS significantly inhibited differentiation and lipogenesis of 3T3-L1 adipocytes in a dose-dependent manner. MCPS suppressed the mRNA expressions of cytidine-cytidine-adenosine-adenosine-thymidine(CCAAT)/enhancer binding proteins ¥á(C/EBP¥á), C/EBP ¥â, C/EBP¥ä, and peroxisome proliferator-activated receptor ¥ã(PPAR¥ã) genes related to the induction of adipose differentiation. MCPS inhibited the mRNA expressions of adipose-specific aP2, adipsin, lipoprotein lipase(LPL), CD36, TGF-¥â, and leptin genes related to the fat formation. MCPS downregulated the mRNA expressions of liver X receptor(LXR) ¥á and fatty acid synthase(FAS) genes related to the induction of lipogenesis. In addition, MCPS reduced the production of adipocyte-induced pro-inflammatory cytokines.

Conclusions : MCPS could regulate the accumulation of lipids and expression of adipogenic genes via inhibition of transcript factors related to induction of adipose differentiation.
KEYWORD
Mahuang-Chuanwu(Mahwang-Cheonoh) Pharmacopuncture (MCP), 3T3-L1 adipocytes, differentiation, adipogenesis,
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