Effects of Korean white ginseng extracts on obesity in high-fat diet-induced obese mice

被引:54
作者
Lee, Young-Sil [2 ]
Cha, Byung-Yoon [2 ]
Yamaguchi, Kohji [2 ]
Choi, Sun-Sil [2 ]
Yonezawa, Takayuki [2 ]
Teruya, Toshiaki [2 ]
Nagai, Kazuo [1 ,2 ]
Woo, Je-Tae [1 ,2 ]
机构
[1] Chubu Univ, Dept Biol Chem, Aichi 4878501, Japan
[2] Chubu Univ, Res Inst Biol Funct, Aichi 4878501, Japan
关键词
Korean white ginseng; High-fat diet-induced obese mice; Lipogenesis-related genes; Intestinal fat absorption; PPAR-GAMMA; TRIGLYCERIDE SYNTHESIS; GENE-EXPRESSION; LIPOPROTEIN-LIPASE; LIPID-METABOLISM; RED GINSENG; CHOLESTEROL; MECHANISMS; RESISTANCE; NUTRITION;
D O I
10.1007/s10616-010-9288-7
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 [微生物学]; 090105 [作物生产系统与生态工程];
摘要
The present study examined the anti-obesity effect and mechanism of action of Korean white ginseng extracts (KGE) using high-fat diet (HFD)-induced obese mice. Mice were fed a low-fat diet (LFD), HFD or HFD containing 0.8 and 1.6% (w/w) KGE diet (HFD + 0.8KGE and HFD + 1.6KGE) for 8 weeks. We also examined the effects of KGE on plasma triglyceride (TG) elevation in mice administrated with oral lipid emulsion. Body weight gain and white adipose tissue (WAT) weight were significantly decreased in the HFD + 1.6KGE group, compared with the HFD group. The plasma TG levels were also significantly reduced in both HFD + 0.8KGE and HFD + 1.6KGE groups, while leptin levels were significantly decreased in only the HFD + 1.6KGE group, compared with the HFD group. The HFD + 1.6KGE group showed significantly lower mRNA levels of lipogenesis-related genes, including peroxisome proliferator-activated receptor gamma 2 (PPAR gamma 2), sterol regulatory element binding protein-1c (SREBP-1c), lipoprotein lipase (LPL), fatty acid synthase (FAS) and diacylglycerol acyltransferase 1 (DGAT1), compared with the HFD group. In addition, a dose of 1000 mg/kg KGE inhibited the elevation of plasma TG levels compared with mice given the lipid emulsion alone. These results suggest that the anti-obesity effects of KGE may be elicited by regulating expression of lipogenesis-related genes in WAT and by delaying intestinal fat absorption.
引用
收藏
页码:367 / 376
页数:10
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