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首页> 外文期刊>Archives of Toxicology >Species difference in the induction of hepatic CYP1A subfamily enzymes, especially CYP1A2, by 2-methoxy-4-nitroaniline among rats, mice, and guinea pigs.
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Species difference in the induction of hepatic CYP1A subfamily enzymes, especially CYP1A2, by 2-methoxy-4-nitroaniline among rats, mice, and guinea pigs.

机译:2-甲氧基-4-硝基苯胺在大鼠,小鼠和豚鼠中诱导肝脏CYP1A亚家族酶,尤其是CYP1A2的物种差异。

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Species difference in the induction of hepatic cytochrome P450 CYP1A subfamily enzymes by 2-methoxy-4-nitroaniline (2-MeO-4-NA) was investigated among male F344 rats, C57BL/6 Cr mice, and Hartley guinea pigs. All species of animals were treated with a single ip injection of 2-MeO-4-NA (0.44 mmol/kg body weight), and changes in levels of the mRNA and protein of hepatic cytochrome P4501A (CYP1A) subfamily enzymes were examined by the methods of RT-PCR and Western blot, respectively. In addition, hepatic microsomal enzyme activities were measured using methoxyresorufin and ethoxyresorufin as substrates of CYP1A2 and CYP1A1, respectively. The overall results of the RT-PCR, Western blot, and measurement of the enzyme activity indicated that 2-MeO-4-NA-mediated induction of hepatic CYP1A subfamily enzymes, especially CYP1A2, occurred only in rats but not any other species of animals examined and that the species difference in the CYP1A induction was not necessarily correlated with that in pharmacokinetics of2-MeO-4-NA. Furthermore, a luciferase reporter gene assay for screening of the ligands of arylhydrocarbon receptor (AhR) using a rat hepatic cell line suggested that 2-MeO-4-NA is not an AhR ligand. The present findings demonstrate for the first time the species difference in the 2-MeO-4-NA-mediated induction of hepatic CYP1A subfamily enzymes between rats and other rodents, mice and guinea pigs, and further propose an AhR-independent pathway for 2-MeO-4-NA-mediated induction in rats.
机译:研究了雄性F344大鼠,C57BL / 6 Cr小鼠和Hartley豚鼠对2-甲氧基-4-硝基苯胺(2-MeO-4-NA)诱导的肝细胞色素P450 CYP1A亚家族酶种类的差异。所有动物种类均经腹膜内注射2-MeO-4-NA(0.44 mmol / kg体重)进行治疗,并通过肝细胞色素P4501A(CYP1A)亚家族酶的mRNA和蛋白质水平进行了检测。分别采用RT-PCR和Western blot方法。此外,分别使用甲氧异氟丁酸和乙氧异氟丁酸作为CYP1A2和CYP1A1的底物来测量肝微粒体酶活性。 RT-PCR,Western印迹和酶活性测量的总体结果表明,2-MeO-4-NA介导的肝CYP1A亚家族酶(尤其是CYP1A2)的诱导仅在大鼠中发生,而在其他任何动物中均未发生审查和CYP1A诱导物种差异不一定与2-MeO-4-NA的药代动力学相关。此外,使用大鼠肝细胞系筛选芳基碳氢化合物受体(AhR)配体的荧光素酶报告基因测定表明2-MeO-4-NA不是AhR配体。本发现首次证明了大鼠与其他啮齿动物,小鼠和豚鼠之间2-MeO-4-NA介导的肝CYP1A亚家族酶诱导的物种差异,并进一步提出了2-的非AhR依赖性途径MeO-4-NA介导的大鼠诱导。

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