Silibinin Capsules improves high fat diet-induced nonalcoholic fatty liver disease in hamsters through modifying hepatic de novo lipogenesis and fatty acid oxidation

脂肪生成 非酒精性脂肪肝 内科学 内分泌学 脂解 脂肪肝 水飞蓟宾 脂肪酸合成 脂肪变性 安普克 β氧化 脂肪酸合酶 化学 脂肪酸 医学 生物化学 脂质代谢 药理学 蛋白激酶A 脂肪组织 新陈代谢 激酶 疾病
作者
Chun-Xue Cui,Jingna Deng,Li Yan,Yuying Liu,Jing‐Yu Fan,Hongna Mu,Hao-Yu Sun,Ying-Hong Wang,Jing‐Yan Han
出处
期刊:Journal of Ethnopharmacology [Elsevier]
卷期号:208: 24-35 被引量:46
标识
DOI:10.1016/j.jep.2017.06.030
摘要

Silibinin Capsules (SC) is a silybin-phospholipid complex with silybin as the bioactive component. Silybin accounts for 50-70% of the seed extract of Silybum marianum (L.) Gaertn.. As a traditional medicine, silybin has been used for treatment of liver diseases and is known to provide a wide range of hepatoprotective effects.High fat diet (HFD)-induced nonalcoholic fatty liver disease (NAFLD) is a worldwide health problem. This study was to investigate the role of SC in NAFLD with focusing on its underlying mechanism and likely target.Male hamsters (Cricetidae) received HFD for 10 weeks to establish NAFLD model. NAFLD was assessed by biochemical assays, histology and immunohistochemistry. Proton nuclear magnetic resonance spectroscopy and western blot were conducted to gain insight into the mechanism.Hamsters fed HFD for 10 weeks developed fatty liver accompanying with increased triglyceride (TG) accumulation, enhancing de novo lipogenesis, increase in fatty acid (FA) uptake and reducing FA oxidation and TG lipolysis, as well as a decrease in the expression of phospho-adenosine monophosphate activated protein kinase α (p-AMPKα) and Sirt 1. SC treatment at 50mg/kg silybin and 100mg/kg silybin for 8 weeks protected hamsters from development of fatty liver, reducing de novo lipogenesis and increasing FA oxidation and p-AMPKα expression, while having no effect on FA uptake and TG lipolysis.SC protected against NAFLD in hamsters by inhibition of de novo lipogenesis and promotion of FA oxidation, which was likely mediated by activation of AMPKα.
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