2-硝基芴在大鼠肝匀浆S-9组分作用下的还原代谢

初步研究了在氮气保护无氧条件下,经Aroclor1254诱导的大鼠肝微粒体酶对2-硝基芴的还原代谢过程.对代谢体系及条件进行了选择用HPLC对代谢产物进行分离研究,经保留时间及紫外光谱核对显示2-硝基芴的主要还原代谢产物为2-氨基芴,除此之外还有三个量少的其代谢产物形成,因含量低而尚未进行结构鉴定.

REDUCTIVE METABOLISM OF ENVIRONMENTAL CARCINOGEN 2-NITRO-FLUORENE BY RAT LIVER S-9 FRACTIONS

Nitro polycyclic aromatic hydrocarbons such as 1-nitro-pyrene, 2-nitro-fluorene, 6-nitro-benzoa]pyrene and 4-nitro-biphenyl have been proved to be carcinogenic in mammalian assays. The mechanism of carcinogenesis is thought to be mediated by the metabolic reduction of these nitro compounds to reactive hydroxylamine intermediates by mammalian liver, lung,nasal tissue and intestinal microflo-ra. In this paper reductive metabolism of 2-nitro-fluorene by rat liver enzyme induced by Aroclor 1254 has been investigated under nitrogen atmosphere. The metabolites have been isolated by reversed phase HPLC and identified by comparison of their chromatogra-phic and UV spectral properties with the authentic compounds. The results show that the reductive metabolism of 2-nitro-fluorene yields mainly 2-amino-fluorene (a well-known carcinogen) plus three minor products, which remain unidentified because of insufficient quantities. The results of this study also confirm the complexity of the metabolic activation pathways.