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用叔丁基对苯二酚或3-(3'-叔丁基-4'-羟基苯基)丙基硫代磺酸钠处理的小鼠肝脏中药物代谢系统和信号转导通路的基因表达谱

The gene expression profile of a drug metabolism system and signal transduction pathways in the liver of mice treated with tert-butylhydroquinone or 3-(3'-tert-butyl-4'-hydroxyphenyl)propylthiosulfonate of sodium.

作者信息

Shintyapina Alexandra B, Vavilin Valentin A, Safronova Olga G, Lyakhovich Vyacheslav V

机构信息

Institute of Molecular Biology and Biophysics, Novosibirsk, Russia.

Novosibirsk State University, Novosibirsk, Russia.

出版信息

PLoS One. 2017 May 3;12(5):e0176939. doi: 10.1371/journal.pone.0176939. eCollection 2017.

Abstract

Tert-butylhydroquinone (tBHQ) is a highly effective phenolic antioxidant used in edible oils and fats in foods as well as in medicines and cosmetics. TBHQ has been shown to have both chemoprotective and carcinogenic effects. Furthermore, it has potential anti-inflammatory, antiatherogenic, and neuroprotective activities. TBHQ induces phase II detoxification enzymes via the Keap1/Nrf2/ARE mechanism, which contributes to its chemopreventive functions. Nonetheless, there is growing evidence that biological effects of tBHQ may be mediated by Nrf2-independent mechanisms related to various signaling cascades. Here, we studied changes in gene expression of phase I, II, and III drug metabolizing enzymes/transporters as well as protein levels and activities of cytochromes P450 (CYPs) elicited by tBHQ and its structural homolog TS-13 in the mouse liver. Next, we carried out gene expression analysis to identify signal transduction pathways modulated by the antioxidants. Mice received 100 mg/kg tBHQ or TS-13 per day or only vehicle. The liver was collected at 12 hours and after 7 days of the treatment. Protein and total RNA were extracted. Gene expression was analyzed using Mouse Drug Metabolism and Signal Transduction PathwayFinder RT2Profiler™PCR Arrays. A western blot analysis was used to measure protein levels and a fluorometric assay was employed to study activities of CYPs. Genes that were affected more than 1.5-fold by tBHQ or TS-13 treatment compared with vehicle were identified. Analysis of the gene expression data revealed changes in various genes that are important for drug metabolism, cellular defense mechanisms, inflammation, apoptosis, and cell cycle regulation. Novel target genes were identified, including xenobiotic metabolism genes encoding CYPs, phase II/III drug metabolizing enzymes/transporters. For Cyp1a2 and Cyp2b, we observed an increase in protein levels and activities during tBHQ or TS-13 treatment. Changes were found in the gene expression regulated by NFκB, androgen, retinoic acid, PI3K/AKT, Wnt, Hedgehog and other pathways.

摘要

叔丁基对苯二酚(tBHQ)是一种高效的酚类抗氧化剂,用于食品中的食用油脂以及药品和化妆品中。已证明TBHQ具有化学保护作用和致癌作用。此外,它还具有潜在的抗炎、抗动脉粥样硬化和神经保护活性。TBHQ通过Keap1/Nrf2/ARE机制诱导II期解毒酶,这有助于其化学预防功能。然而,越来越多的证据表明,tBHQ的生物学效应可能由与各种信号级联相关的非Nrf2依赖性机制介导。在此,我们研究了tBHQ及其结构类似物TS-13在小鼠肝脏中引起的I、II和III期药物代谢酶/转运蛋白的基因表达变化以及细胞色素P450(CYPs)的蛋白质水平和活性。接下来,我们进行基因表达分析以确定抗氧化剂调节的信号转导途径。小鼠每天接受100 mg/kg tBHQ或TS-13,或仅接受赋形剂。在治疗12小时和7天后收集肝脏。提取蛋白质和总RNA。使用小鼠药物代谢和信号转导途径Finder RT2Profiler™PCR阵列分析基因表达。采用蛋白质印迹分析来测量蛋白质水平,并采用荧光测定法研究CYPs的活性。确定了与赋形剂相比,受tBHQ或TS-13处理影响超过1.5倍的基因。基因表达数据分析揭示了各种对药物代谢、细胞防御机制、炎症、细胞凋亡和细胞周期调节重要的基因的变化。鉴定了新的靶基因,包括编码CYPs的外源性代谢基因、II/III期药物代谢酶/转运蛋白。对于Cyp1a2和Cyp2b,我们观察到在tBHQ或TS-13处理期间蛋白质水平和活性增加。在由NFκB、雄激素、视黄酸、PI3K/AKT、Wnt、Hedgehog和其他途径调节的基因表达中发现了变化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cce9/5415222/1c7f88c03a17/pone.0176939.g001.jpg

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