Suppr超能文献

膳食植物化学吲哚类物 I3C 和 DIM 的药效学:诱导 Nrf2 介导的 II 相药物代谢和抗氧化基因,并与异硫氰酸盐协同作用。

Pharmacodynamics of dietary phytochemical indoles I3C and DIM: Induction of Nrf2-mediated phase II drug metabolizing and antioxidant genes and synergism with isothiocyanates.

机构信息

Department of Pharmaceutics, Ernest Mario School of Pharmacy, Rutgers, The State University of New Jersey, Piscataway, NJ 08854, USA.

出版信息

Biopharm Drug Dispos. 2011 Jul;32(5):289-300. doi: 10.1002/bdd.759. Epub 2011 Jun 8.

Abstract

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 µm I3C + 1 µm SFN, 6.25 µm I3C + 1 µm PEITC and 6.25 µm DIM + 1 µm PEITC, while an additive effect was observed for 6.25 µm DIM + 1 µm 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.

摘要

抗氧化反应元件 (ARE) 是许多 II 相药物代谢酶 (DME)、III 相转运蛋白和抗氧化酶表达的关键调节元件,由转录因子 Nrf2 介导。本研究旨在研究存在于十字花科蔬菜中的四种常见植物化学物质;吲哚:吲哚-3-甲醇 (I3C)、3,3'-二吲哚甲烷 (DIM);和异硫氰酸酯 (ITC):苯乙基异硫氰酸酯 (PEITC) 和萝卜硫素 (SFN) 之间 Nrf2-ARE 介导的转录活性的潜在激活和协同作用。在人肝癌细胞系 (HepG2-C8) 中测定化合物的细胞毒性。计算合并指数以评估对 ARE 介导的基因表达诱导的协同作用。采用定量实时聚合酶链反应 (qPCR) 测量 Nrf2 和 Nrf2 介导基因的 mRNA 表达。I3C 和 DIM 的细胞毒性低于 SFN 和 PEITC。与 I3C 相比,DIM 被发现是一种更强的 ARE 诱导剂。在 6.25 µm I3C + 1 µm SFN、6.25 µm I3C + 1 µm PEITC 和 6.25 µm DIM + 1 µm PEITC 的联合处理后观察到协同作用,而在 6.25 µm DIM + 1 µm SFN 中观察到相加作用。还观察到内源性 Nrf2、II 相基因 (GSTm2、UGT1A1 和 NQO1) 和抗氧化基因 (HO-1 和 SOD1) 的诱导。总之,单独的吲哚 I3C 或 DIM 或与 ITCs SFN 或 PEITC 联合诱导,可诱导 Nrf2-ARE 介导的基因表达,这可能增强癌症化学预防活性。

相似文献

引用本文的文献

本文引用的文献

4
Cancer chemoprevention mechanisms mediated through the Keap1-Nrf2 pathway.癌症化学预防机制通过 Keap1-Nrf2 通路介导。
Antioxid Redox Signal. 2010 Dec 1;13(11):1713-48. doi: 10.1089/ars.2010.3221. Epub 2010 Aug 14.
8
Targeting NRF2 signaling for cancer chemoprevention.针对 NRF2 信号通路的癌症化学预防。
Toxicol Appl Pharmacol. 2010 Apr 1;244(1):66-76. doi: 10.1016/j.taap.2009.08.028. Epub 2009 Sep 2.
10
Reactive oxygen species-dependent signaling regulates cancer.活性氧物种依赖性信号传导调控癌症。
Cell Mol Life Sci. 2009 Dec;66(23):3663-73. doi: 10.1007/s00018-009-0099-y. Epub 2009 Jul 24.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验