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Species Difference among Experimental Rodents in the Activity and Induction of Cytochrome P‐450 Isozymes for Mutagenic Activation of Carcinogenic Aromatic Amines

机译:实验性啮齿动物在致癌性芳香胺诱变活化的细胞色素P-450同工酶活性和诱导中的物种差异

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摘要

The expressions of hepatic microsomal cytochrome P‐450 isozymes in male rats, mice, hamsters and guinea pigs were studied comparatively with or without an ip injection of a cytochrome P‐450 inducer. The activity and quantity of microsomal cytochrome P‐450 isozymes were determined respectively by a bacterial mutation assay with TA98 and immunochemical assays using monoclonal antibodies against rat cytochrome P‐450 isozymes. 3‐Methoxy‐4‐aminoazobenzene (3‐MeO‐AAB), 2‐amino‐3‐methyl‐9 ‐pyrido[2,3‐ ]indole acetate (MeAαC) and 3‐methylcholanthrene were used as cytochrome P‐450 inducers, and 7 carcinogenic aromatic amines including 3‐MeO‐AAB and MeAαC were used as substrates for the mutation assay. By means of these assays, we examined the species differences among rodents in the activity and induction rate of hepatic cytochrome P‐450 isozymes responsible for the mutagenic activation of carcinogenic aromatic amines.
机译:比较研究了腹腔注射或不注射细胞色素P-450诱导剂的雄性大鼠,小鼠,仓鼠和豚鼠肝微粒体细胞色素P-450同工酶的表达。微粒体细胞色素P‐450同工酶的活性和数量分别通过TA98的细菌突变测定和使用针对大鼠细胞色素P‐450同工酶的单克隆抗体的免疫化学测定来确定。 3-甲氧基-4-氨基偶氮苯(3-MeO-AAB),2-氨基-3-甲基-9-吡啶并[2,3-]乙酸吲哚酯(MeAαC)和3-甲基胆固醇被用作细胞色素P-450诱导剂,使用7种致癌性芳香胺(包括3-MeO-AAB和MeAαC)作为突变分析的底物。通过这些测定,我们检查了啮齿类动物之间的物种差异,这些差异是引起致癌芳香胺诱变活化的肝细胞色素P-450同工酶的活性和诱导率。

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