Coumarin attenuates hepatic steatosis by down-regulating lipogenic gene expression in mice fed a high-fat diet

被引:37
|
作者
Um, Min Young [1 ]
Moon, Mi Kyeong [1 ]
Ahn, Jiyun [1 ]
Ha, Tae Youl [1 ]
机构
[1] Korea Food Res Inst, Div Metab & Funct Res, Songnam 463746, South Korea
关键词
Coumarin; High-fat diet; Hepatic steatosis; Lipogenesis; LIVER-DISEASE; INSULIN-RESISTANCE; LIPID-METABOLISM; RATS; OBESITY; ACIDS; ADIPONECTIN; DERIVATIVES;
D O I
10.1017/S0007114512005260
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
Coumarin is a natural compound abundant in plant-based foods such as citrus fruits, tomatoes, vegetables and green tea. Although coumarin has been reported to exhibit anti-coagulant, anti-inflammation and cholesterol-lowering properties, the effect of coumarin on hepatic lipid metabolism remains unclear. In the present study, we evaluated the ability of coumarin to protect against hepatic steatosis associated with a high-fat diet (HFD) and investigated potential mechanisms underlying this effect. C57BL/6J mice were fed a normal diet, HFD and HFD containing 0.05% courmarin for 8 weeks. The present results showed that coumarin reduced weight gain and abdominal fat mass in mice fed the HFD for 8 weeks (P<0.05). Coumarin also significantly reduced the HFD-induced elevation in total cholesterol, apoB, leptin and insulin (P<0.05). In the liver of HFD-fed mice, coumarin significantly reduced total lipids, TAG and cholesterol (38, 22 and 9% reductions, respectively; P<0.05), as well as lipid droplet number and size. Additionally, thiobarbituric acid-reactive substance levels, as an indicator of hepatic steatosis, were attenuated by coumarin (P<0.05). Finally, coumarin suppressed the HFD-induced up-regulation in fatty acid synthase (FAS) activity, and the expression of sterol regulatory element-binding protein-1, FAS, acetyl-CoA carboxylase 1, PPAR gamma and CCAAT/enhancer-binding protein-alpha in the liver. Taken together, these results demonstrate that coumarin could prevent HFD-induced hepatic steatosis by regulating lipogenic gene expression, suggesting potential targets for preventing hepatic steatosis.
引用
收藏
页码:1590 / 1597
页数:8
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