Fonshteĭn L M, Revazova Iu A, Zolotareva G N, Abilev S K, Akin'shina L N
Genetika. 1978 May;14(5):900-8.
A previous evaluation of mutagenic activity of some drugs and perspective substances is carried out using indicator microorganisms. The mutagenicity of dioxydine, a drag with discovered antibacterial activity, is investigated. Dioxydine is shown to induce reversions in mutant of Salmonella typhimurium TA-1950, the indicator strain which demonstrates mutagenic activity of agents, producing mutations of base pair substitution type. Dioxydine proved to affect logariphmiically growing bacterial culture with great activity. Mutageni effect of dioxydine is not modified itself in microsomal oxidation system in vitro. Some data concerning participation of excision reparation enzyme (uvr-B+ gene product) in repair of lethal damages induced by dioxydine, have been obtained. The dioxydine ability to cause bacterial gene mutations in host mediated assay as well as dominant and recessive sex-linked lethal mutations in Drosophila is demonstrated. Dioxydine is capable of inducing chromosome aberrations in bone marrow cells and dominant lethal mutations in mouse germ cells.
先前使用指示微生物对一些药物和潜在物质的致突变活性进行了评估。对已发现具有抗菌活性的药物二氧嘧啶的致突变性进行了研究。结果表明,二氧嘧啶可诱导鼠伤寒沙门氏菌TA-1950突变体发生回复突变,该指示菌株可显示产生碱基对替代型突变的试剂的致突变活性。事实证明,二氧嘧啶对对数生长期的细菌培养物具有很强的活性影响。二氧嘧啶的诱变作用在体外微粒体氧化系统中本身不会改变。已获得一些有关切除修复酶(uvr-B+基因产物)参与修复由二氧嘧啶诱导的致死性损伤的数据。证明了二氧嘧啶在宿主介导试验中引起细菌基因突变以及在果蝇中引起显性和隐性性连锁致死突变的能力。二氧嘧啶能够诱导骨髓细胞中的染色体畸变和小鼠生殖细胞中的显性致死突变。