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首页> 外文期刊>Biopharmaceutics and Drug Disposition >Pharmacodynamics of dietary phytochemical indoles I3C and DIM: Induction of Nrf2-mediated phase II drug metabolizing and antioxidant genes and synergism with isothiocyanates.
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Pharmacodynamics of dietary phytochemical indoles I3C and DIM: Induction of Nrf2-mediated phase II drug metabolizing and antioxidant genes and synergism with isothiocyanates.

机译:膳食植物化学吲哚I3C和DIM的药效学:诱导Nrf2介导的II期药物代谢和抗氧化基因以及与异硫氰酸酯的协同作用。

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摘要

The antioxidant response element (ARE) is a critical regulatory element for the expression of many phase II drug metabolizing enzymes (DME), phase III transporters and antioxidant enzymes, mediated by the transcription factor Nrf2. The aim of this study was to examine the potential activation and synergism of Nrf2-ARE-mediated transcriptional activity between four common phytochemicals present in cruciferous vegetables; the indoles: indole-3-carbinol (I3C), 3,3'-diindolylmethane (DIM); and the isothiocyanates (ITCs): phenethyl isothiocyanate (PEITC) and sulforaphane (SFN). The cytotoxicity of the compounds was determined in a human liver hepatoma cell line (HepG2-C8). The combination index was calculated to assess the synergistic effects on the induction of ARE-mediated gene expressions. Quantitative real-time polymerase chain reaction (qPCR) was employed to measure the mRNA expressions of Nrf2 and Nrf2-mediated genes. I3C and DIM showed less cytotoxicity than SFN and PEITC. Compared with I3C, DIM was found to be a stronger inducer of ARE. Synergism was observed after combined treatments of 6.25 microm I3C + 1 microm SFN, 6.25 microm I3C + 1 microm PEITC and 6.25 microm DIM + 1 microm PEITC, while an additive effect was observed for 6.25 microm DIM + 1 microm SFN. Induction of endogenous Nrf2, phase II genes (GSTm2, UGT1A1 and NQO1) and antioxidant genes (HO-1 and SOD1) was also observed. In summary, the indole I3C or DIM alone could induce or syngergistically induce in combination with the ITCs SFN or PEITC, Nrf2-ARE-mediated gene expression, which could potentially enhance cancer chemopreventive activity.
机译:抗氧化反应元件(ARE)是转录因子Nrf2介导的许多II期药物代谢酶(DME),III期转运蛋白和抗氧化酶表达的关键调控元件。这项研究的目的是检查十字花科蔬菜中存在的四种常见植物化学物质之间Nrf2-ARE介导的转录活性的潜在激活和协同作用。吲哚:吲哚-3-甲醇(I3C),3,3'-二吲哚甲烷(DIM);异硫氰酸酯(ITC):异硫氰酸苯乙基酯(PEITC)和萝卜硫烷(SFN)。在人肝肝癌细胞系(HepG2-C8)中确定了化合物的细胞毒性。计算组合指数以评估诱导ARE介导的基因表达的协同作用。定量实时聚合酶链反应(qPCR)用于测量Nrf2和Nrf2介导的基因的mRNA表达。 I3C和DIM的细胞毒性低于SFN和PEITC。与I3C相比,发现DIM是ARE的更强诱导剂。联合处理6.25微米I3C + 1微米SFN,6.25微米I3C + 1微米PEITC和6.25微米DIM + 1微米PEITC后,观察到协同作用,而对6.25微米DIM + 1微米SFN观察到累加效应。还观察到内源性Nrf2,II期基因(GSTm2,UGT1A1和NQO1)和抗氧化剂基因(HO-1和SOD1)的诱导。总之,单独使用吲哚I3C或DIM可以与ITC SFN或PEITC结合诱导或协同诱导Nrf2-ARE介导的基因表达,从而可能增强癌症的化学预防活性。

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