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Effects of pomegranate peel polyphenols on lipid accumulation and cholesterol metabolic transformation in L-02 human hepatic cells via the PPAR gamma-ABCA1/CYP7A1 pathway

机译:石榴皮多酚对P-02γ-ABCA1/ CYP7A1途径对L-02人肝细胞脂质积累和胆固醇代谢转化的影响

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摘要

To study the effect of pomegranate peel polyphenols on lipid accumulation and cholesterol metabolic transformation in human hepatic cells, purified pomegranate peel polyphenols (PPPs), their main component, punicalagin (PC), and the metabolite of PC, pomegranate ellagic acid (PEA), were chosen as the polyphenols to be tested. At the same time the human hepatocyte cell line L-02 was selected as the experimental cell and a model of steatotic L-02 hepatocytes in vitro was constructed in this paper. The results showed that PPPs, PC and PEA in different concentrations could decrease the total cholesterol (TC) content and increase the total bile acid (TBA) content, and so possess a lipid-lowering effect. The order of the lipid-lowering effect from strong to weak is PEA > PPPs > PC. The relative mRNA expression of peroxisome proliferator-activated receptor. (PPAR.), ATP-binding cassette transporter A1 (ABCA1) and cholesterol 7 alpha hydroxylase (CYP7A1) was up-regulated by PPPs, PC and PEA in a dose-dependent manner. The effect on the relative mRNA expression can be listed in descending order as: PEA > PPPs > PC. Similar results were found in a western blot analysis. The PPAR. protein, ABCA1 protein and CYP7A1 protein were up-regulated in L-02 cells treated with the three tested polyphenols. All the results indicated that PPPs, PC and PEA could regulate upstream the expression of PPAR., ABCA1 and CYP7A1, both at transcript and protein levels, to activate the PPAR gamma-ABCA1/CYP7A1 cell signaling pathway and enhance cholesterol metabolism in L-02 cells. Therefore, PPPs, as a kind of natural material, may be paid more attention in the prevention and treatment of diseases related to excessive cholesterol accumulation.
机译:为了研究石榴皮多酚对人肝细胞中脂质蓄积和胆固醇代谢转化的影响,研究了石榴皮多酚(PPPs),其主要成分punicalagin(PC)以及PC的代谢产物石榴皮鞣花酸(PEA),选择作为被测试的多酚。同时,以人肝细胞L-02为实验细胞,构建了脂肪肝L-02肝细胞模型。结果表明,不同浓度的PPPs,PC和PEA可以降低总胆固醇(TC)含量并增加总胆汁酸(TBA)含量,因此具有降脂作用。降脂作用从强到弱的顺序是PEA> PPPs> PC。过氧化物酶体增殖物激活受体的相对mRNA表达。 (PPAR。),ATP结合盒转运蛋白A1(ABCA1)和胆固醇7α羟化酶(CYP7A1)被PPPs,PC和PEA呈剂量依赖性上调。对相对mRNA表达的影响可以降序列出:PEA> PPPs> PC。在蛋白质印迹分析中发现了相似的结果。 PPAR。在用三种测试的多酚处理的L-02细胞中,蛋白,ABCA1蛋白和CYP7A1蛋白上调。所有结果表明,PPPs,PC和PEA可以在转录和蛋白水平上调节PPAR,ABCA1和CYP7A1的上游表达,从而激活PPARγ-ABCA1/ CYP7A1细胞信号通路并增强L-02中的胆固醇代谢细胞。因此,PPPs作为一种天然物质,在预防和治疗与胆固醇过多积聚有关的疾病中可能会受到更多关注。

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