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首页> 外文期刊>Biochemical Pharmacology >Role of nuclear factor-erythroid 2-related factor 2 (Nrf2) in the transcriptional regulation of brain ABC transporters during acute acetaminophen (APAP) intoxication in mice
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Role of nuclear factor-erythroid 2-related factor 2 (Nrf2) in the transcriptional regulation of brain ABC transporters during acute acetaminophen (APAP) intoxication in mice

机译:小鼠对乙酰氨基酚中毒期间核因子-类胡萝卜素2相关因子2(Nrf2)在脑ABC转运蛋白的转录调控中的作用

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Changes in expression of liver ABC transporters have been described during acute APAP intoxication. However, the effect of APAP on brain ABC transporters is poorly understood. The aim of this study was to evaluate the effect of APAP on brain ABC transporters expression and the role of the oxidative stress sensor Nrf2. Male C57BL/6J mice were administered APAP (400 mg/kg) for analysis of brain mRNA and protein expression of Mrp1-6, Bcrp and P-gp. The results show induction of P-gp, Mrp2 and Mrp4 proteins, with no changes in Bcrp, Mrp1 or Mrp5-6. The protein values were accompanied by corresponding changes in mRNA levels. Additionally, brain Nrf2 nuclear translocation and expression of two Nrf2 target genes, NAD(P)H:quinone oxidoreductase 1 (Nqo1) and Hemoxygenase 1 (Ho-1), was evaluated at 6, 12 and 24 h after APAP treatment. Nrf2 nuclear content increased by 58% at 12 h after APAP along with significant increments in mRNA and protein expression of Nqo1 and Ho-1. Furthermore, APAP treated Nrf2 knockout mice did not increase mRNA or protein expression of Mrp2 and Mrp4 as observed in wildtypes. In contrast, P-gp induction by APAP was observed in both genotypes. In conclusion, acute APAP intoxication induces protein expression of brain P-gp, Mrp2 and Mrp4. This study also suggests that brain changes in Mrp2 and Mrp4 expression may be due to in situ Nrf2 activation by APAP, while P-gp induction is independent of Nrf2 function. The functional consequences of these changes in brain ABC transporters by APAP deserve further attention. (C) 2015 Elsevier Inc. All rights reserved.
机译:急性APAP中毒期间已描述了肝脏ABC转运蛋白表达的变化。但是,APAP对大脑ABC转运蛋白的作用了解甚少。这项研究的目的是评估APAP对脑ABC转运蛋白表达的影响以及氧化应激传感器Nrf2的作用。给雄性C57BL / 6J小鼠APAP(400 mg / kg),以分析脑mRNA和Mrp1-6,Bcrp和P-gp蛋白的表达。结果表明诱导了P-gp,Mrp2和Mrp4蛋白,而Bcrp,Mrp1或Mrp5-6没有变化。蛋白质值伴随着mRNA水平的相应变化。此外,在APAP治疗后的6、12和24小时,评估了大脑Nrf2核易位和两个Nrf2靶基因NAD(P)H:醌氧化还原酶1(Nqo1)和Hemoxygenase 1(Ho-1)的表达。 APr后12小时,Nrf2核含量增加了58%,同时Nqo1和Ho-1的mRNA和蛋白质表达也显着增加。此外,APAP处理的Nrf2基因敲除小鼠没有增加野生型中所观察到的Mrp2和Mrp4的mRNA或蛋白质表达。相反,在两种基因型中均观察到APAP诱导的P-gp。总之,急性APAP中毒诱导脑P-gp,Mrp2和Mrp4的蛋白表达。这项研究还表明,Mrp2和Mrp4表达的大脑变化可能归因于APAP原位激活Nrf2,而P-gp诱导与Nrf2功能无关。由APAP引起的这些大脑ABC转运蛋白改变的功能后果值得进一步关注。 (C)2015 Elsevier Inc.保留所有权利。

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