非那嗪和氨基非那嗪类药物在果蝇体内的遗传毒性通过翅斑试验和dna修复试验进行了研究

Tetsushi Watanabe, Terue Kasai, Mikito Arima, Kazuko Okumura, Naoyoshi Kawabe, Teruhisa Hirayama
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引用次数: 14

摘要

研究了6种非那嗪和氨基非那嗪衍生物在果蝇翅斑和dna修复中的遗传毒性和dna损伤活性。非那嗪(Pz)和所有被试的氨基那嗪,即1-氨基那嗪(APz)、2-APz、2,3-二氨基那嗪(DAPz)、2,7-DAPz和2,7-二氨基-3,8-二甲基那嗪(DADMPz),在翅膀斑点试验中表现出显著的致突变性。机翼斑点试验中的活动按顺序排列。(2,7- dapz, 2,3- dapz) >(2-APz - 1-APz, Pz)。在dna修复试验中,2,3- dapz、2,7- dapz和DADMPz明显表现出dna损伤活性,而Pz、1-APz和2- apz则无活性。基于这些结果,我们预测DADMPz, 2,3- dapz和2,7- dapz可能比2- apz, 1-APz或Pz更致癌。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Genotixicity in vivo of phenazine and aminophenazines assayed in the wing spot test and the DNA-repair test with Drosophila melanogaster

The genotoxicity and DNA-damaging activity of 6 phenazine and aminophenazine derivatives were assayed in the wing spot and DNA-repair tests in Drosophila melanogaster. Phenazine (Pz), and all aminophenazines tested, namely, 1-aminophenazine (APz), 2-APz, 2,3-diaminophenazine (DAPz), 2,7-DAPz and 2,7-diamino-3,8-dimethylphenazine (DADMPz), exhibited mutagenicity significantly in the wing spot test. The activities in the wing spot test were ranked in a sequence DADMPz > (2,7-DAPz, 2,3-DAPz) > (2-APz 1-APz, Pz). In the DNA-repair test, 2,3-DAPz, 2,7-DAPz, and DADMPz clearly showed DNA-damaging activity, but Pz, 1-APz and 2-APz were inactive. Based on these results, we predict that DADMPz, 2,3-DAPz and 2,7-DAPz are likely to be more carcinogenic than 2-APz, 1-APz or Pz.

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