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首页> 外文期刊>Archives of Toxicology >Effect of 4-tert-octylphenol on cytochrome P450 enzymes in rat liver.
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Effect of 4-tert-octylphenol on cytochrome P450 enzymes in rat liver.

机译:4-叔辛基苯酚对大鼠肝脏细胞色素P450酶的影响。

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摘要

The effects were studied of 4-tert-octylphenol (OP) on hepatic cytochrome P450 enzymes in rats. Rats were treated intraperitoneally with OP twice, at doses of 5, 10, and 20 mg/kg. Among the cytochrome P450-dependent monooxygenase activities, testosterone 2alpha-hydroxylase activity, which is associated with CYP2C11, was significantly decreased by OP at all doses. The level relative to control activity was 67-22%. CYP3A2-dependent monooxygenase, testosterone 6beta-hydroxylase activity was also decreased by 51% by OP at 20 mg/kg. Furthermore, immunoblotting showed that OP (10 or 20 mg/kg) significantly decreased CYP2C11/6 and CYP3A2/1 protein levels. However, the reduction ratio of CYP2C11/6 and CYP3A2/1 protein levels by OP treatment was lower than that of testosterone 2alpha-hydroxylase and testosterone 6beta-hydroxylase activities. The Cl(int) (Vmax/Km) value for testosterone 2alpha-hydroxylase was significantly decreased by OP at all doses, whereas the Cl(int) value for testosterone 6beta-hydroxylase was only decreased by OP at 20 mg/kg. In addition, 7-ethoxycoumarin O-deethylase activity was significantly decreased by 32% by the highest dose of OP. By contrast, CYP1A1-, CYP1A2-, CYP2A1-, CYP2B1/2-, CYP2D1-, CYP2E1- and CYP4A1/2/3-dependent monooxygenase activities were not affected by OP at any dose. These results suggest that OP changes the male-specific cytochrome P450 isoforms in rat liver, and that these changes closely relate to the toxicity of OP.
机译:研究了4-叔辛基苯酚(OP)对大鼠肝细胞色素P450酶的影响。大鼠以5、10和20 mg / kg的剂量腹膜内注射OP两次。在细胞色素P450依赖的单加氧酶活性中,与CYP2C11相关的睾丸激素2α-羟化酶活性在所有剂量下均显着降低。相对于对照活性的水平是67-22%。 CYP3A2依赖性单加氧酶,睾丸酮6β-羟化酶活性在20 mg / kg下被OP降低了51%。此外,免疫印迹显示OP(10或20 mg / kg)显着降低CYP2C11 / 6和CYP3A2 / 1蛋白水平。然而,通过OP处理,CYP2C11 / 6和CYP3A2 / 1蛋白水平的降低率低于睾丸激素2α-羟化酶和睾丸激素6β-羟化酶的降低率。在所有剂量下,睾丸酮2α-羟化酶的Cl(int)(Vmax / Km)值均被OP显着降低,而在20 mg / kg下,睾丸酮6β-羟化酶的Cl(int)值仅被OP降低。此外,最高剂量的OP可显着降低7-乙氧基香豆素O-脱乙基酶的活性。与此相反,CYP1A1,CYP1A2-,CYP2A1-,CYP2B1 / 2-,CYP2D1-,CYP2E1-和CYP4A1 / 2/3依赖的单加氧酶活性不受任何剂量OP的影响。这些结果表明,OP改变了大鼠肝脏中雄性特异性细胞色素P450亚型,这些变化与OP的毒性密切相关。

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