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中国药学(英文版) ›› 2014, Vol. 23 ›› Issue (6): 361-368.DOI: 10.5246/jcps.2014.06.049

• 【研究论文】 • 上一篇    下一篇

三七总皂苷对慢性酒精性脂肪肝的保护作用研究

丁仁博, 鲍娇琳, 曹怡纬, 何承伟, 王一涛, 万建波*   

  1. 澳门大学 中药质量研究国家重点实验室 中华医药研究院, 中国 澳门 999078
  • 收稿日期:2014-04-22 修回日期:2014-05-06 出版日期:2014-06-28 发布日期:2014-05-10
  • 通讯作者: Tel.: +853-3974873, Fax: +853-28841358
  • 基金资助:
    Research Committee of the University of Macau (Grant No. MYRG123-ICMS12 and MYRG111-ICMS13) and from Macao Science and Technology Development Fund (Grant No. 010/2013/A1).

Panax notoginseng saponins protect against chronic ethanol-induced hepatic steatosis

Renbo Ding, Jiaolin Bao, Yiwei Cao, Chengwei He, Yitao Wang, Jianbo Wan*   

  1. State Key Laboratory of Quality Research in Chinese Medicine, Institute of Chinese Medical Sciences, University of Macau, Macao 999078, China
  • Received:2014-04-22 Revised:2014-05-06 Online:2014-06-28 Published:2014-05-10
  • Contact: Tel.: +853-3974873, Fax: +853-28841358
  • Supported by:
    Research Committee of the University of Macau (Grant No. MYRG123-ICMS12 and MYRG111-ICMS13) and from Macao Science and Technology Development Fund (Grant No. 010/2013/A1).

摘要:

长期酗酒可以诱导脂肪肝的形成, 本文旨在研究三七总皂苷对慢性酒精诱导脂肪肝的保护作用及其机理。将小鼠随机分为三组, 分别给予含有酒精的Lieber-DeCarli液体饲料, 混合200 mg/kg/BW的三七总皂苷的酒精Lieber-DeCarli液体饲料, 和对照Lieber-DeCarli液体饲料, 连续饲喂8, 结果显示三七总皂苷能够明显地抑制慢性酒精所导致的肝脂质堆积; 同时, 三七总皂苷可以明显降低血浆甘油三酯水平, 血浆ALTAST酶活力, 以及肝组织TNF-αIL-6水平。三总皂苷不仅通过下调磷酸化HSL而抑制白色脂肪组织脂解, 而且可以抑制肝摄取脂肪酸的关键CD36基因的表达。结果表明三七总皂苷可以通过改善白色脂肪组织的脂质代谢紊乱和降低炎症因子的产生, 发挥对慢性酒精性脂肪肝的保护作用

关键词: 酒精性脂肪肝, 三七总皂苷, 脂肪分解, 炎症

Abstract: Chronic alcohol consumption induces hepatic steatosis, the early stage of alcoholic liver disease (ALD). The aim of present study is to investigate the protective effect of Panax notoginseng saponins (PNS) against chronic ethanol-induced hepatic steatosis in vivo. Mice were pair-fed a modified Lieber-DeCarli liquid diet containing alcohol or isocaloric maltose dextrin as control diet with or without PNS (200 mg/kg, BW) for 8 weeks. Animals supplemented with PNS were protected against hepatic lipid accumulation induced by chronic ethanol exposure. Accordingly, PNS could significantly decrease the elevation of plasma triglyceride, plasma enzyme activities, i.e. alanine aminotransferase (ALT) and aspartate aminotransferase (AST), and hepatic TNF-α and IL-6 levels which were induced by chronic alcohol exposure. In addition, PNS markedly reduced the lipolysis of white adipose tissue (WAT) that stimulated by alcohol feeding through the inhibiting protein expression of phosphorylation of hormone-sensitive lipase (p-HSL), rather than total HSL. Furthermore, alcohol exposure also enhanced fatty acid uptake capacity in liver by elevated hepatic CD36 expression, which could attenuated by PNS treatment. These results demonstrate that PNS supplementation protects against chronic ethanol-induced hepatic steatosis, which is associated with ameliorating dysfunctional lipid metabolism of WAT and the reduced inflammatory cytokines. Our findings suggested that PNS might be potential to be developed as an effective agent for the treatment of chronic alcoholic steatosis.

Key words: Alcoholic fatty liver, Panax notoginseng saponins, Lipolysis, Inflammation

中图分类号: 

Supporting: Research Committee of the University of Macau (Grant No. MYRG123-ICMS12 and MYRG111-ICMS13) and from Macao Science and Technology Development Fund (Grant No. 010/2013/A1).