Noguchi T, Fong K L, Lai E K, Alexander S S, King M M, Olson L, Poyer J L, McCay P B
Biochem Pharmacol. 1982 Mar 1;31(5):615-24. doi: 10.1016/0006-2952(82)90440-3.
Evidence is presented which demonstrates that the first polypeptide to disappear in liver microsomes of phenobarbital-induced rats treated with CC14 was the 52,000 dalton p-450 cytochrome. Data are also presented which show that this form of cytochrome P-450 was capable of generating the trichloromethyl radical from CCl4 in a reconstituted system containing the purified cytochrome, NADPH-cytochrome P-450 reductase, NADPH, CCl4, and the spin-trapping agent, phenyl-t-butyl nitrone. Other cytochrome P-450 fractions not containing the 52,000 dalton form did not produce this radical. The formation of this highly reactive radical may have resulted in localized damage to the cytochrome, causing the cytochrome either to be released from the microsomal membrane or to form large aggregates which did not migrate in the gel electrophoretic procedures employed.
有证据表明,在用四氯化碳处理的苯巴比妥诱导大鼠的肝微粒体中,首先消失的多肽是52,000道尔顿的P-450细胞色素。还提供了数据表明,在含有纯化的细胞色素、NADPH-细胞色素P-450还原酶、NADPH、四氯化碳和自旋捕获剂苯基叔丁基硝酮的重构系统中,这种形式的细胞色素P-450能够从四氯化碳生成三氯甲基自由基。其他不包含52,000道尔顿形式的细胞色素P-450组分不会产生这种自由基。这种高反应性自由基的形成可能导致细胞色素的局部损伤,导致细胞色素要么从微粒体膜释放,要么形成在所用凝胶电泳程序中不迁移的大聚集体。