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高脂饮食小鼠高丽红参提取物的脂代谢作用。

Lipid metabolic effect of Korean red ginseng extract in mice fed on a high-fat diet.

机构信息

Korea Ginseng Corporation Ginseng Research Institute, Yuseong-gu, Daejeon, Korea.

出版信息

J Sci Food Agric. 2012 Jan 30;92(2):388-96. doi: 10.1002/jsfa.4589. Epub 2011 Sep 14.

Abstract

BACKGROUND

Ginseng saponin and ginsenosides exert anti-obesity effects via the modulation of physiological lipid metabolism in vivo or intracellular signalling in cell culture systems. However, the complicated relationship between the anti-obesity effects of ginseng and gene expression has yet to be defined under in vivo conditions. Therefore, we evaluated the relationship between the anti-obesity effects of Korean red ginseng extract (KRGE) and hepatic gene expression profiles in mice fed long-term on a high-fat diet (HFD) in this study.

RESULTS

KRGE reduces the levels of cholesterol, low-density lipoprotein-cholesterol (LDL-C), serum triglycerides, and atherogenic indices. Levels of leptin, adiponectin and insulin, which regulate glucose and lipid metabolism, were impaired profoundly by HFD. However, KRGE treatment brought these levels back to normal. KRGE was found to down-regulate genes associated with lipid metabolism or cholesterol metabolism (Lipa, Cyp7a1, Il1rn, Acot2, Mogat1, Osbpl3, Asah3l, Insig1, Anxa2, Vldlr, Hmgcs1, Sytl4, Plscr4, Pla2g4e, Slc27a3, Enpp6), all of which were up-regulated by HFD.

CONCLUSION

KRGE regulated the expression of genes associated with abnormal physiology via HFD. Leptin, insulin, and adiponectin, which carry out critical functions in energy and lipid metabolism, were shown to be modulated by KRGE. These results show that KRGE is effective in preventing obesity.

摘要

背景

人参皂苷和人参皂甙通过调节体内生理脂质代谢或细胞培养系统中的细胞内信号来发挥抗肥胖作用。然而,在体内条件下,人参的抗肥胖作用与基因表达之间的复杂关系尚未得到明确。因此,我们在本研究中评估了长期给予高脂肪饮食(HFD)的小鼠中,高丽红参提取物(KRGE)的抗肥胖作用与肝基因表达谱之间的关系。

结果

KRGE 降低胆固醇、低密度脂蛋白胆固醇(LDL-C)、血清甘油三酯和动脉粥样硬化指数水平。调节葡萄糖和脂质代谢的瘦素、脂联素和胰岛素水平因 HFD 而严重受损。然而,KRGE 处理使这些水平恢复正常。发现 KRGE 下调与脂质代谢或胆固醇代谢相关的基因(Lipa、Cyp7a1、Il1rn、Acot2、Mogat1、Osbpl3、Asah3l、Insig1、Anxa2、Vldlr、Hmgcs1、Sytl4、Plscr4、Pla2g4e、Slc27a3、Enpp6),这些基因均因 HFD 而上调。

结论

KRGE 通过 HFD 调节与异常生理相关的基因表达。瘦素、胰岛素和脂联素在能量和脂质代谢中发挥关键作用,被证明可被 KRGE 调节。这些结果表明 KRGE 可有效预防肥胖。

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