Ghanem Carolina I, Rudraiah Swetha, Bataille Amy M, Vigo María B, Goedken Michael J, Manautou José E
Instituto de Investigaciones Farmacológicas (ININFA), Facultad de Farmacia y Bioquímica, CONICET, Universidad de Buenos Aires, Buenos Aires, Argentina; Cátedra de Fisiopatología. Facultad de Farmacia y Bioquímica, Universidad de Buenos Aires, Buenos Aires, Argentina.
Department of Pharmaceutical Sciences, University of Connecticut, Storrs, CT, United States.
Biochem Pharmacol. 2015 Apr 1;94(3):203-11. doi: 10.1016/j.bcp.2015.01.013. Epub 2015 Feb 7.
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 (400mg/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 24h after APAP treatment. Nrf2 nuclear content increased by 58% at 12h 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.
在急性对乙酰氨基酚中毒期间,肝脏ABC转运蛋白的表达变化已有报道。然而,对乙酰氨基酚对脑ABC转运蛋白的影响却知之甚少。本研究的目的是评估对乙酰氨基酚对脑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小鼠注射对乙酰氨基酚(400mg/kg),以分析脑Mrp1 - 6、Bcrp和P - gp的mRNA和蛋白表达。结果显示P - gp、Mrp2和Mrp4蛋白被诱导,而Bcrp、Mrp1或Mrp5 - 6无变化。蛋白值伴随着mRNA水平的相应变化。此外,在对乙酰氨基酚处理后6、12和24小时评估脑Nrf2核转位以及两个Nrf2靶基因,即NAD(P)H:醌氧化还原酶1(Nqo1)和血红素加氧酶1(Ho - 1)的表达。对乙酰氨基酚处理后12小时,Nrf2核含量增加了58%,同时Nqo1和Ho - 1的mRNA和蛋白表达显著增加。此外,与野生型小鼠不同,对乙酰氨基酚处理的Nrf2基因敲除小鼠未增加Mrp2和Mrp4的mRNA或蛋白表达。相反,在两种基因型中均观察到对乙酰氨基酚诱导P - gp。总之,急性对乙酰氨基酚中毒诱导脑P - gp、Mrp2和Mrp4的蛋白表达。本研究还表明,脑Mrp2和Mrp4表达的变化可能是由于对乙酰氨基酚原位激活Nrf2所致,而P - gp的诱导与Nrf2功能无关。对乙酰氨基酚引起的脑ABC转运蛋白这些变化的功能后果值得进一步关注。