AI Article Synopsis

  • Quinoxaline-1,4-dioxides (QdNOs) like mequindox (MEQ) exhibit significant biological activities, but their mutagenic effects were highlighted in various tests according to OECD guidelines.
  • MEQ and carbadox (CBX) showed strong mutagenicity in tests including Salmonella reverse mutation and chromosome aberration, with MEQ displaying slightly higher genotoxic potential than CBX.
  • The study is important as it reveals the genotoxic risks associated with MEQ for the first time, while also confirming known risks of CBX concerning QdNO derivatives.

Article Abstract

Quinoxaline-1,4-dioxides (QdNOs) are the potent heterocyclic N-oxides with interesting biological properties such as antibacterial, anticandida, antitubercular, anticancer and antiprotozoal activities. Here, we tested and compared the mequindox (MEQ) for mutagenic abilities in a battery of different short term tests according to OECD guidelines. When compared with the controls, a strong mutagenicity of MEQ and carbadox (CBX) was observed with an approximate concentration-effect relationship in Salmonella reverse mutation test, chromosome aberration test, unscheduled DNA synthesis assay and HGPRT gene mutation test, in the absence and presence of S(9)-mix. In in vivo micronucleus test, CBX produced significant increase in the proportion of micronucleus formation than MEQ in mice bone marrow cells. From these results, we can conclude that MEQ had a strong genotoxic potential to mammalian cells in vitro as well as in vivo and its mutagenicity is slightly higher than CBX. Our results, for the 1st time, discuss the genotoxic potential of MEQ. These results not only confirm the earlier findings about CBX but also extend the knowledge and awareness about the genotoxic risk of QdNO derivatives.

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Source
http://dx.doi.org/10.1016/j.fct.2012.10.003DOI Listing

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