Pandey Manoj K, Yadav Sanjay, Parmar Devendra, Das Mukul
Food Toxicology Laboratory, Industrial Toxicology Research Centre, MG Marg, PO Box 80, Lucknow-226001, India.
Toxicol Appl Pharmacol. 2006 Jun 1;213(2):126-34. doi: 10.1016/j.taap.2005.09.013. Epub 2005 Nov 2.
In the present study the effect of repeated fish fried oil (RFFO) and its extract (RFFE) on hepatic cytochrome P450 (CYP) isozymes, benzo(a)pyrene (BP) metabolism and DNA adduct formation was undertaken. HPLC analysis of RFFO showed the presence of several polycyclic aromatic hydrocarbons. CYP in microsomes from control and RFFO-treated animals showed a peak at 450 nm; however, a shift of 2 nm in the SORET region along with significant induction was observed in microsomes prepared from 3-methylcholanthrene (MC)- and RFFE-treated animals. Activities of hepatic ethoxyresorufin-O-deethylase, methoxyresorufin-O-deethylase, aryl hydrocarbon hydroxylase and erythromycin-N-demethylase were found to be significantly (P < 0.05) induced following exposure of RFFE, whereas none of these enzymes were altered in RFFO-treated group. Immunoblot analysis revealed that RFFE and MC were potent inducers of CYP1A1, 1A1/2 and 3A1 isozymes, where as RFFO showed no change in these protein levels. RT-PCR analysis showed induction of cDNA of CYP1A1 and CYP3A1 by RFFE treatment. Hepatic microsomes prepared from RFFE exposed animals enhanced BP metabolism with a concomitant increase in the relative proportion of BP 7,8-diol. Hepatic microsomes prepared from animals pretreated with RFFE and MC significantly enhanced the binding of [(3)H]-BP to calf thymus DNA. The overall results suggest that exposure to RFFE may induce hepatic CYP isozymes thereby producing enhanced reactive metabolites with a potential to bind with DNA that may result in cancer.
在本研究中,对重复使用的油炸鱼油(RFFO)及其提取物(RFFE)对肝细胞色素P450(CYP)同工酶、苯并(a)芘(BP)代谢及DNA加合物形成的影响进行了研究。RFFO的高效液相色谱分析显示存在几种多环芳烃。对照动物和经RFFO处理动物的微粒体中的CYP在450nm处有一个峰值;然而,在由3-甲基胆蒽(MC)和RFFE处理动物制备的微粒体中,观察到在SORET区域有2nm的位移以及显著的诱导作用。在暴露于RFFE后,发现肝乙氧基试卤灵-O-脱乙基酶、甲氧基试卤灵-O-脱乙基酶、芳烃羟化酶和红霉素-N-脱甲基酶的活性显著(P<0.05)诱导,而在RFFO处理组中这些酶均未改变。免疫印迹分析显示,RFFE和MC是CYP1A1、1A1/2和3A1同工酶的有效诱导剂,而RFFO在这些蛋白质水平上未显示变化。逆转录-聚合酶链反应(RT-PCR)分析显示RFFE处理可诱导CYP1A1和CYP3A1的cDNA。由暴露于RFFE的动物制备的肝微粒体增强了BP代谢,同时BP 7,8-二醇的相对比例增加。由用RFFE和MC预处理的动物制备的肝微粒体显著增强了[(3)H]-BP与小牛胸腺DNA的结合。总体结果表明,暴露于RFFE可能诱导肝CYP同工酶,从而产生增强的反应性代谢产物,这些代谢产物有可能与DNA结合,可能导致癌症。