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7H-二苯并[c,g]咔唑及其代谢产物在鼠伤寒沙门氏菌中的致突变性。

Mutagenicity of 7H-dibenzo[c,g]carbazole and metabolites in Salmonella typhimurium.

作者信息

Schoeny R, Warshawsky D

出版信息

Mutat Res. 1987 Aug;188(4):275-86. doi: 10.1016/0165-1218(87)90004-8.

Abstract

7H-Dibenzo[c,g]carbazole (DBC) is a potent carcinogen of environmental import. Reverse-mutation plate-incorporation assays for mutagenicity were undertaken in Salmonella typhimurium strains TA98 and TA100. Results were negative when no exogenous activation system was used, as well as when assays incorporated liver homogenates (S9) from rats, mice and rabbits. By contrast DBC was mutagenic in a forward mutation assay in Salmonella strain TM677 using resistance to 8-azaguanine for selection. Metabolites of DBC were generated by incubation with rat-liver microsomes and separated by HPLC. Two of these metabolites were directly mutagenic for Salmonella strain TM 677 while two others were mutagenic upon addition of S9. Synthetic phenolic derivatives of DBC were also mutagenic in this assay when further metabolized. It is likely that metabolites of DBC phenols constitute the biologically active forms.

摘要

7H - 二苯并[c,g]咔唑(DBC)是一种具有环境重要性的强效致癌物。在鼠伤寒沙门氏菌TA98和TA100菌株中进行了致突变性的反向突变平板掺入试验。当不使用外源激活系统时,以及当试验掺入大鼠、小鼠和兔子的肝脏匀浆(S9)时,结果均为阴性。相比之下,在沙门氏菌TM677菌株的正向突变试验中,利用对8 - 氮杂鸟嘌呤的抗性进行选择时,DBC具有致突变性。DBC的代谢产物通过与大鼠肝脏微粒体孵育产生,并通过高效液相色谱法分离。其中两种代谢产物对沙门氏菌TM677具有直接致突变性,而另外两种在添加S9后具有致突变性。DBC的合成酚类衍生物在进一步代谢后在该试验中也具有致突变性。DBC酚类的代谢产物很可能构成了生物活性形式。

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