Sidorova Y A, Grishanova A Y, Lyakhovich V V
Institute of Molecular Biology and Biophysics, Siberian Division of Russian Academy of Medical Sciences, Timakova str. 2, Novosibirsk 630090, Russia.
Toxicol Lett. 2005 Feb 15;155(2):253-8. doi: 10.1016/j.toxlet.2004.10.001.
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.
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。