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噻虫嗪杀虫剂及其制剂产品对黑腹果蝇体细胞的诱变、重组和致癌潜力。

Mutagenic, recombinogenic and carcinogenic potential of thiamethoxam insecticide and formulated product in somatic cells of Drosophila melanogaster.

作者信息

de Morais Cássio Resende, Carvalho Stephan Malfitano, Carvalho Naves Maria Paula, Araujo Galber, de Rezende Alexandre Azenha Alves, Bonetti Ana Maria, Spanó Mário Antônio

机构信息

Institute of Genetics and Biochemistry, Federal University of Uberlândia, Campus Umuarama, 38900-402, Uberlândia, Minas Gerais, Brazil.

Department of Entomology, Federal University of Lavras, PO Box 3037, 37200-000, Lavras, Minas Gerais, Brazil.

出版信息

Chemosphere. 2017 Nov;187:163-172. doi: 10.1016/j.chemosphere.2017.08.108. Epub 2017 Aug 19.

Abstract

Thiamethoxam (TMX) belongs to a class of neuro-active insecticides referred as neonicotinoids, while actara (AC) is one of the most popular TMX-based products in Brazil. The aim of this study was to evaluate the mutagenic, recombinogenic and carcinogenic potential of TMX and AC insecticides. The mutagenic and recombinogenic effect of TMX and AC were evaluated in vivo by the Somatic Mutation and Recombination Test (SMART) while carcinogenic effects were evaluated through the Test for Detection of Epithelial Tumor Clones (wts test), both in somatic cells of Drosophila melanogaster. In the SMART, third instar larvae from standard (ST) and high bioactivation (HB) crosses were treated with different concentrations of TMX and AC (2.4; 4.8; 9.7 × 10 mM and 1.9 × 10 mM). The results revealed mutagenic effects at the highest concentrations tested in the HB cross. In the test for the detection of epithelial tumor, third instar larvae resulting from the cross between wts/TM3, Sb virgin females and mwh/mwh males were treated with the same concentrations of TMX and AC used in the SMART. No carcinogenic effect was observed at any of the concentrations tested. In this work, the inhibition of the mechanism of repair by homologous recombination was observed in flies exposed to 9.7 × 10 and 1.9 × 10 mM of AC. In conclusion, TMX and AC demonstrated to be a promutagen in the highest concentrations tested.

摘要

噻虫嗪(TMX)属于一类被称为新烟碱类的神经活性杀虫剂,而阿克泰(AC)是巴西最受欢迎的基于噻虫嗪的产品之一。本研究的目的是评估噻虫嗪和阿克泰杀虫剂的致突变性、重组性和致癌性。通过体细胞突变和重组试验(SMART)在体内评估噻虫嗪和阿克泰的致突变性和重组性,同时通过上皮肿瘤克隆检测试验(wts试验)在黑腹果蝇的体细胞中评估致癌性。在SMART试验中,用不同浓度的噻虫嗪和阿克泰(2.4;4.8;9.7×10 mM和1.9×10 mM)处理标准(ST)和高生物活化(HB)杂交的三龄幼虫。结果显示在HB杂交试验中测试的最高浓度下有诱变作用。在上皮肿瘤检测试验中,用SMART试验中使用的相同浓度的噻虫嗪和阿克泰处理wts/TM3、Sb处女雌蝇和mwh/mwh雄蝇杂交产生的三龄幼虫。在任何测试浓度下均未观察到致癌作用。在这项研究中,在暴露于9.7×10和1.9×10 mM阿克泰的果蝇中观察到同源重组修复机制受到抑制。总之,噻虫嗪和阿克泰在测试的最高浓度下表现出促突变性。

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