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

Abstract

1. 1. 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. 2. 2. Male guinea-pigs weighing 500–700 g were administered 3-methylcholanthrene (25mg/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. 3. 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. 4. 4. 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. 5. 5. Cytochrome P-450 content of guinea-pig liver microsomes were increased significantly about 2.5-lbld 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.