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

Authors :
Alexandre Azenha Alves de Rezende
Stephan Malfitano Carvalho
Maria Paula Carvalho Naves
Galber R. Araujo
Ana Maria Bonetti
Cássio Resende de Morais
Mário Antônio Spanó
Source :
Chemosphere. 187:163-172
Publication Year :
2017
Publisher :
Elsevier BV, 2017.

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 × 10−4 mM and 1.9 × 10−3 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, Sb1 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 × 10−4 and 1.9 × 10−3 mM of AC. In conclusion, TMX and AC demonstrated to be a promutagen in the highest concentrations tested.

Details

ISSN :
00456535
Volume :
187
Database :
OpenAIRE
Journal :
Chemosphere
Accession number :
edsair.doi.dedup.....4d2017ff227237afd2bfb90eb1b9ebb3
Full Text :
https://doi.org/10.1016/j.chemosphere.2017.08.108