International Journal of Molecular Sciences (Jun 2023)

DNA Damage Estimation after Chronic and Combined Exposure to Endocrine Disruptors: An In Vivo Real-Life Risk Simulation Approach

  • Vasiliki Karzi,
  • Eren Ozcagli,
  • Manolis N. Tzatzarakis,
  • Elena Vakonaki,
  • Irene Fragkiadoulaki,
  • Aikaterini Kalliantasi,
  • Christina Chalkiadaki,
  • Athanasios Alegakis,
  • Polychronis Stivaktakis,
  • Aikaterini Karzi,
  • Antonios Makrigiannakis,
  • Anca Oana Docea,
  • Daniela Calina,
  • Aristidis Tsatsakis

DOI
https://doi.org/10.3390/ijms24129989
Journal volume & issue
Vol. 24, no. 12
p. 9989

Abstract

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Exposure to chemical substances has always been a matter of concern for the scientific community. During the last few years, researchers have been focusing on studying the effects resulting from combined exposure to different substances. In this study, we aimed to determine the DNA damage caused after chronic and combined exposure to substances characterized as endocrine disruptors using comet and micronuclei assays, specifically glyphosate (pure and commercial form), bisphenol A, parabens (methyl-, propyl- and butylparaben), triclosan and bis (2-ethylhexyl) phthalate. The highest mean tail intensity was observed in the group exposed to a high-dose (10 × ADI) mixture of substances (Group 3), with a mean value of 11.97 (11.26–13.90), while statistically significant differences were noticed between the groups exposed to low-dose (1 × ADI) (Group 2) and high-dose (10 × ADI) (Group 3) mixtures of substances (p = 0.003), and between Group 3 and both groups exposed to high doses (10 × ADI) of the pure and commercial forms of glyphosate (Groups 4 (p = 0.014) and 5 (p = 0.007)). The micronuclei assay results were moderately correlated with the exposure period. Group 5 was the most impacted exposure group at all sampling times, with mean MN counts ranging between 28.75 ± 1.71 and 60.75 ± 1.71, followed by Group 3 (18.25 ± 1.50–45.75 ± 1.71), showing that commercial forms of glyphosate additives as well as mixtures of endocrine disruptors can enhance MN formation. All exposure groups showed statistically significant differences in micronuclei counts with an increasing time trend.

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