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3-甲基胆蒽、苯巴比妥、除虫菊和2,4,5-T异辛酯对豚鼠肝脏、肺和肾脏微粒体混合功能氧化酶系统的体内效应:一项比较研究。

In vivo effects of 3-methylcholanthrene, phenobarbital, pyrethrum and 2,4,5-T isooctylester on liver, lung and kidney microsomal mixed-function oxidase system of guinea-pig: a comparative study.

作者信息

Işcan M, Arinç E, Vural N, Işcan M Y

出版信息

Comp Biochem Physiol C Comp Pharmacol Toxicol. 1984;77(1):177-90. doi: 10.1016/0742-8413(84)90149-x.

Abstract

The optimum conditions (pH, microsomal protein amount and substrate concentration) of guinea-pig liver, lung and kidney microsomal aniline 4-hydroxylase, ethylmorphine N-demethylase and benzo[a]pyrene hydroxylase activities were determined. Male guinea-pigs weighing 500-700 g were administered 3-methylcholanthrene (25 mg/kg, i.p. 3 days), phenobarbital (75 mg/kg, i.p. 3 days), pyrethrum (120 mg/kg, i.p. 2 days) and 2,4,5-T isooctylester (200 mg/kg, i.p. 3 days). 3-Methylcholanthrene treatment caused significant increases in liver microsomal benzo[a]pyrene hydroxylase and kidney microsomal aniline 4-hydroxylase activities. However, with phenobarbital treatment the only significant increase was observed in liver microsomal ethylmorphine N-demethylase activity. Pyrethrum treatment decreased kidney microsomal ethylmorphine N-demethylase activity significantly. 2,4,5-T isooctylester treatment increased liver microsomal aniline 4-hydroxylase and lung microsomal ethylmorphine N-demethylase activities significantly. Liver microsomal NADPH-cytochrome c reductase activity was increased significantly by phenobarbital and pyrethrum treatment. The other treatments did not cause any significant changes in microsomal NADPH-cytochrome c reductase activities of liver, lung and kidney. Cytochrome P-450 content of guinea-pig liver microsomes were increased significantly about 2.5-fold and 2-fold by treatment with 3-methylcholanthrene and phenobarbital, respectively. 3-Methylcholanthrene also caused 1 nm spectral shift in the absorption maxima of CO difference spectrum of the dithionite-reduced liver microsomal cytochrome P-450, forming P-449.

摘要

测定了豚鼠肝脏、肺和肾脏微粒体中苯胺4-羟化酶、N-脱甲基乙吗啡酶和苯并[a]芘羟化酶活性的最佳条件(pH值、微粒体蛋白量和底物浓度)。对体重500 - 700克的雄性豚鼠分别腹腔注射3-甲基胆蒽(25毫克/千克,连续3天)、苯巴比妥(75毫克/千克,连续3天)、除虫菊(120毫克/千克,连续2天)和2,4,5-T异辛酯(200毫克/千克,连续3天)。3-甲基胆蒽处理使肝脏微粒体苯并[a]芘羟化酶和肾脏微粒体苯胺4-羟化酶活性显著增加。然而,苯巴比妥处理仅使肝脏微粒体N-脱甲基乙吗啡酶活性有显著增加。除虫菊处理使肾脏微粒体N-脱甲基乙吗啡酶活性显著降低。2,4,5-T异辛酯处理使肝脏微粒体苯胺4-羟化酶和肺微粒体N-脱甲基乙吗啡酶活性显著增加。苯巴比妥和除虫菊处理使肝脏微粒体NADPH-细胞色素c还原酶活性显著增加。其他处理对肝脏、肺和肾脏微粒体NADPH-细胞色素c还原酶活性未引起任何显著变化。3-甲基胆蒽和苯巴比妥处理分别使豚鼠肝脏微粒体细胞色素P-450含量显著增加约2.5倍和2倍。3-甲基胆蒽还使连二亚硫酸盐还原的肝脏微粒体细胞色素P-450的CO差光谱吸收最大值发生1纳米的光谱位移,形成P-449。

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