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甲萘醌对大鼠肝脏CYP1A1和CYP1A2的诱导作用。

Rat hepatic CYP1A1 and CYP1A2 induction by menadione.

作者信息

Sidorova Y A, Grishanova A Y, Lyakhovich V V

机构信息

Institute of Molecular Biology and Biophysics, Siberian Division of Russian Academy of Medical Sciences, Timakova str. 2, Novosibirsk 630090, Russia.

出版信息

Toxicol Lett. 2005 Feb 15;155(2):253-8. doi: 10.1016/j.toxlet.2004.10.001.

Abstract

The effects of menadione on activities and expression of cytochrome P450 (CYP) 1A subfamily (CYP1A) isozymes in rat hepatic tissue were examined. When rats were treated orally with 15 mg/kg menadione for 4 days, the elevation of hepatic CYP1A1/1A2 specific activities in microsomal preparations was detected with approximately 5.4- and 2.5-fold increase over control values for ethoxyresorufin-O-deethylase (EROD, CYP1A1) and methoxyresorufin-O-demethylase (MROD, CYP1A2) activities, respectively. CYP1A1 and CYP1A2 mRNA levels in the liver of menadione-treated rats were approximately 11.8- and 1.8-fold higher than in controls, respectively, whereas the expression of the CYP1A regulatory proteins aryl hydrocarbon-receptor (AhR) and AhR nuclear translocator (Arnt) was not changed at the mRNA level. The result of this study demonstrates that menadione induces CYP1A1/1A2 expression in vivo through either transcriptional activation and/or mRNA stabilization.

摘要

研究了甲萘醌对大鼠肝组织中细胞色素P450(CYP)1A亚家族(CYP1A)同工酶活性及表达的影响。当大鼠口服15 mg/kg甲萘醌,连续给药4天时,微粒体制剂中肝CYP1A1/1A2的比活性升高,乙氧异吩恶唑酮-O-脱乙基酶(EROD,CYP1A1)和甲氧基异吩恶唑酮-O-脱甲基酶(MROD,CYP1A2)活性分别比对照值增加约5.4倍和2.5倍。甲萘醌处理的大鼠肝脏中CYP1A1和CYP1A2的mRNA水平分别比对照高约11.8倍和1.8倍,而CYP1A调节蛋白芳烃受体(AhR)和AhR核转运蛋白(Arnt)的mRNA水平没有变化。本研究结果表明,甲萘醌通过转录激活和/或mRNA稳定作用在体内诱导CYP1A1/1A2表达。

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