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首页> 外文期刊>Chemosphere >EFFECT OF 2,4,4'-TRICHLORO-2'-HYDROXYDIPHENYL ETHER ON CYTOCHROME P450 ENZYMES IN THE RAT LIVER
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EFFECT OF 2,4,4'-TRICHLORO-2'-HYDROXYDIPHENYL ETHER ON CYTOCHROME P450 ENZYMES IN THE RAT LIVER

机译:2,4,4'-三氯-2'-羟基二苯醚对大鼠肝脏细胞色素P450酶的影响

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摘要

We examined the effect of 2,4,4'-trichloro-2'-hydroxydiphenyl ether (Irgasan DP300) on microsomal cytochrome P450 (P450) enzymes in rat liver. Rats were treated intraperitoneally with Irgasan DP300 daily for 4 days, at doses of 0.2, 0.4 and 0.8 mmol/kg. Among the P450 dependent monooxygenase activities, 7-benzyloxyresorufin O-debenzylase (BROD) and 7-pentoxyresorufin O-depentylase (PROD) in rats, which are associated with CYP2B1, were remarkably induced by all doses of Irgasan DP300. The relative induction to each control activity were from 5.6- to 22.3-fold and 4.9- to 20.2-fold, respectively. Furthermore, immunoblotting showed that CYP2B1/2 protein level in rat liver microsomes was increased from 10.8- to 34.4 fold by Irgasan DP300. In addittion, 7-ethoxycoumarin O-deethylase (ECOD) and p-nitrophenol hydroxylase (PNPH) activities were significantly increased by Irgasan DP300 at all doses (from 1.4- to 4.9-fold). Although the activities of other P450-dependent monooxygenases, namely aminopyrine N-demethylase (APND), aniline p-hydroxylase (ANPH), erythromycin N-demethylase (EMND), lauric acid omega-hydroxylase (LAOH) and testosterone 6 beta-hydroxylase (TS6BH) were increased at high doses (greater than or equal to 0.4 mmol/kg) of Irgasan DP300, the relative level was lower than those of the CYP2B1-dependent monooxygenases such as BROD and PROD. However, 7-ethoxyresorufin O-deethylase (EROD), 7-methoxyresorufin O-demethylase (MROD), testosterone 2 alpha-hydroxylase (TS2AH) and testosterone 7 alpha-hydroxylase (TS7AH) activities were not affected by any doses of Irgsan DP300. Immunoblotting showed that CYP3A2/1 and CYP4A1 protein levels were significantly induced from 1.3- to 2.2-fold by Irgasan DP300 (greater than or equal to 0.4 mmoll/kg), whereas those of CYP1A1/2, CYP2C11/6 and CYP2E1 were not affected by any doses of Irgasan DP300. These results suggest that Irgasan DP300 induces the P450 isoforms of CYP2B subfamily in the rat liver, and that the induced P450 isozymes closely relates to the toxicity of Irgasan DP300 or its chlorinated derivatives. (C) 1997 Elsevier Science Ltd. [References: 45]
机译:我们检查了2,4,4'-三氯-2'-羟基二苯醚(Irgasan DP300)对大鼠肝脏微粒体细胞色素P450(P450)酶的影响。每天用Irgasan DP300腹膜内处理大鼠,剂量为0.2、0.4和0.8 mmol / kg,为期4天。在P450依赖的单加氧酶活性中,大鼠中的7-苄氧基间苯二酚O-脱苄基酶(BROD)和7-戊氧基间苯二酚O-脱戊基酶(PROD)与CYP2B1相关,被所有剂量的Irgasan DP300显着诱导。对每个对照活性的相对诱导分别是5.6-22.3倍和4.9-20.2倍。此外,免疫印迹表明,通过Irgasan DP300,大鼠肝微粒体中的CYP2B1 / 2蛋白水平从10.8-增加到34.4倍。此外,Irgasan DP300在所有剂量下均显着提高了7-乙氧基香豆素O-脱乙基酶(ECOD)和对硝基苯酚羟化酶(PNPH)的活性(从1.4倍至4.9倍)。尽管其他P450依赖的单加氧酶(即氨基比林N-脱甲基酶(APND),苯胺p-羟化酶(ANPH),红霉素N-脱甲基酶(EMND),月桂酸ω-羟化酶(LAOH)和睾丸激素6β-羟化酶( TS6BH)在高剂量(大于或等于0.4 mmol / kg)的Irgasan DP300中增加,相对水平低于CYP2B1依赖性单加氧酶,例​​如BROD和PROD。但是,任何剂量的Irgsan DP300均不影响7-乙氧基间苯二酚O-脱乙基酶(EROD),7-甲氧基间苯二酚O-脱甲基酶(MROD),睾丸酮2α-羟化酶(TS2AH)和睾丸酮7α-羟化酶(TS7AH)的活性。免疫印迹表明,Irgasan DP300(大于或等于0.4 mmol / kg)显着诱导CYP3A2 / 1和CYP4A1蛋白水平从1.3倍提高到2.2倍,而CYP1A1 / 2,CYP2C11 / 6和CYP2E1则不受影响使用任何剂量的Irgasan DP300。这些结果表明,Irgasan DP300诱导大鼠肝脏中CYP2B亚家族的P450同工型,并且诱导的P450同工酶与Irgasan DP300或其氯代衍生物的毒性密切相关。 (C)1997 Elsevier Science Ltd. [参考:45]

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