Chitosan Oligosaccharides Inhibit Adipogenesis in 3T3-L1 Adipocytes
Á¶ÀºÀç, Atiar Rahman, ±è»ó¿ì, ¹éÀ¯¹Ì, ȲÇýÁø, ¿ÀÁ¤¿µ, ȲÈñ¼±, À̼ºÇÐ, À±Á¾¿ø,
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Á¶ÀºÀç ( Cho Eun-Jae )
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( Atiar Rahman )
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±è»ó¿ì ( Kim Sang-Woo )
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¹éÀ¯¹Ì ( Baek Yu-Mi )
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ȲÇýÁø ( Hwang Hye-Jin )
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¿ÀÁ¤¿µ ( Oh Jung-Young )
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ȲÈñ¼± ( Hwang Hee-Sun )
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À̼ºÇÐ ( Lee Sung-Hak )
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À±Á¾¿ø ( Yun Jong-Won )
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KMID : 0545120080180010080
Abstract
The 3T3-L1 cell line is a well-established and commonly used in vitro model to assess adipocyte differentiation. Over the course of several days, confluent 3T3-L1 cells can be converted to adipocytes in the presence of an adipogenic cocktail. In this study, the effects of chitosan oligosaccharides (CO) on adipocyte differentiation of 3T3-L1 cells were studied. The CO significantly decreased lipid accumulation, a marker of adipogenesis, in a dose-dependent manner. The low molecular mass CO (1-3 kDa) were the most effective at inhibiting adipocyte differentiation. Moreover, mRNA expression levels of both CCAAT/enhancer-binding protein (C/EBP) ¥á and peroxisome proliferator-activated receptor (PPAR) ¥ã, the key adipogenic transcription factors, were markedly decreased by CO treatments. CO also significantly downregulated adipogenic marker proteins such as leptin, adiponectin, and resistin. Our results suggest a role for CO as anti-obesity agents by inhibiting adipocyte differentiation mediated through the downregulated expression of adipogenic transcription factors and other specific genes.
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Adipocyte;chitosan oligosaccharide;obesity;3T3-L1 cell;PPAR¥ã;C/EBP¥á
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