苯醌类药物对艾姆斯沙门氏菌的致突变性研究

Atsushi Hakura, Hisatoshi Mochida, Yoshie Tsutsui, Kiyomi Yamatsu
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引用次数: 19

摘要

采用5种不同的Ames沙门氏菌诱变试验菌株,在S9混合物存在和不存在的情况下,研究了12种简单苯醌(BQ)衍生物的诱变性。使用的7个bq在有和/或没有S9混合的情况下表现出诱变性,并且大多数bq产生了轻微的逆转录增加。对苯醌(p-BQ)对菌株TA104的诱变活性最强(17个诱导复合体/nmol/plate)。对氧化诱变剂敏感的TA104菌株对bq的诱变性最敏感,对大体积DNA加合物敏感的TA2637菌株对bq的诱变性次之。在没有S9混合物的情况下,p-BQ和2,3- dicl -5,6- dicn - bq的诱变性显著降低。这些发现表明,BQ对鼠伤寒沙门氏菌的致突变性可归因于BQ还原后的氧化损伤以及与BQ形成的带有亲电取代基的DNA加合物。
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Mutagenicity of benzoquinones for Ames Salmonella tester strains

The mutagenicity of 12 simple benzoquinone (BQ) derivatives was studied using five different Ames Salmonella mutagenicity tester strains in the presence and absence of S9 mix. Seven of the BQs used displayed mutagenicity with and/or without S9 mix, and most of them produced a marginal increase in revertants. p-Benzoquinone (p-BQ) showed the most potent mutagenic activity (17 induced revertants/nmol/plate for strain TA104 without S9 mix) among the BQs tested. TA104, which is sensitive to oxidative mutagens, was the most sensitive to the mutagenicity of the BQs of the five strains used, while the second most sensitive strain was TA2637, which detects bulky DNA adducts. Significant reductions in the mutagenicity of p-BQ, and 2,3-diCl-5,6-diCN-BQ without S9 mix were observed in the presence of catalase. These findings suggest that the mutagenicity of BQs for S. typhimurium is attributable to oxidative injury after BQ reduction and to DNA adducts that form with BQs that have electrophilic substituents.

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