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藜麦多酚提取物通过抑制脂质积累、炎症和氧化应激缓解非酒精性脂肪肝疾病。

Quinoa Polyphenol Extract Alleviates Non-Alcoholic Fatty Liver Disease via Inhibiting Lipid Accumulation, Inflammation and Oxidative Stress.

机构信息

State Key Laboratory of Food Science and Technology, School of Food Science and Technology, Wuxi 214026, China.

出版信息

Nutrients. 2024 Jul 15;16(14):2276. doi: 10.3390/nu16142276.

Abstract

Recently, the incidence of NAFLD has exploded globally, but there are currently no officially approved medications for treating the condition. The regulation of NAFLD through plant-derived active substances has become a new area of interest. Quinoa ( Willd.) has been discovered to contain a large quantity of bioactive compounds. In this study, we established a free fatty acid (FFA)-induced steatosis model and explored the effects of quinoa polyphenol extract (QPE) on the major hallmarks of NAFLD. The results indicated that QPE significantly reduced intracellular triglyceride (TG) and total cholesterol (TC) levels. Additionally, QPE remarkably elevated the levels of superoxide dismutase (SOD), catalase (CAT) and glutathione (GSH) and lowered levels of malondialdehyde (MDA). Further examination revealed that QPE attenuated intracellular inflammation, which was verified by the reduced levels of pro-inflammatory cytokines. Mechanistically, QPE inhibited fatty acid biosynthesis mainly by targeting de novo lipogenesis (DNL) via the AMPK/SREBP-1c signaling pathway. Moreover, network pharmacology was used to analyze key targets for NAFLD mitigation by ferulic acid (FA), a major component of QPE. Taken together, this study suggests that QPE could ameliorate NAFLD by modulating hepatic lipid metabolism and alleviating oxidative stress and inflammation.

摘要

近年来,NAFLD 的发病率在全球范围内呈爆炸式增长,但目前尚无官方批准的药物可用于治疗该疾病。通过植物来源的活性物质来调节 NAFLD 已成为一个新的研究领域。藜麦(Willd.)中被发现含有大量生物活性化合物。在本研究中,我们建立了游离脂肪酸(FFA)诱导的脂肪变性模型,并探讨了藜麦多酚提取物(QPE)对 NAFLD 主要特征的影响。结果表明,QPE 可显著降低细胞内甘油三酯(TG)和总胆固醇(TC)水平。此外,QPE 还显著提高了超氧化物歧化酶(SOD)、过氧化氢酶(CAT)和谷胱甘肽(GSH)的水平,降低了丙二醛(MDA)的水平。进一步的研究表明,QPE 可减轻细胞内炎症,这一点通过降低促炎细胞因子的水平得到了验证。在机制上,QPE 主要通过 AMPK/SREBP-1c 信号通路抑制从头脂肪生成(DNL)来抑制脂肪酸的合成。此外,网络药理学还分析了 QPE 中的主要成分阿魏酸(FA)对 NAFLD 缓解作用的关键靶点。综上所述,本研究表明,QPE 通过调节肝脂代谢、减轻氧化应激和炎症,可改善 NAFLD。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ac4/11279623/a51852563416/nutrients-16-02276-g001.jpg

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