Correlation Engine 2.0
Clear Search sequence regions


  • apoptosis (1)
  • benzhydryl compounds (2)
  • biota (1)
  • bisphenol (10)
  • bisphenols f (3)
  • cellular (1)
  • GST 4 (1)
  • low (2)
  • phenols (2)
  • SEK 1 (1)
  • SKN 1 (1)
  • toxic effect (1)
  • Sizes of these terms reflect their relevance to your search.

    Bisphenol F (BPF) and bisphenol S (BPS) have been developed as an alternative to bisphenol A (BPA), a well-known endocrine disruptor, leading to their detection in the aquatic environment. In this work, we used the animal model Caenorhabditis elegans to improve our understanding of their potential effects on the biota and the environment. Our findings demonstrated that, after 24 h exposure, all the bisphenols examined increased the number of apoptotic corpses and the expression of the detoxifying enzymes SOD-3 and GST-4, without affecting the ROS levels, while BPA and BPS significantly enhanced DNA fragmentation. Furthermore, similarly to BPA, BPF and BPS did not alter the lifespan through the activation of SEK-1 and SKN-1 pathways. Thus, this study raises the attention of the risks associated with exposure to BPA alternatives. We also examined the effects of microplastic (MP) eluates on C. elegans. Aqueous extracts of weathered microplastic samples, both at high and low degradation state and pellets, have been evaluated for their effects on lifespan, DNA fragmentation, germline apoptosis, and oxidative stress response. Overall, our findings showed that eluates of low degraded plastics exert a greater toxic effect on the nematode C. elegans compared with the aqueous sample of high degraded plastic fragments and pellets.

    Citation

    Graziella Ficociello, Valentina Gerardi, Daniela Uccelletti, Andrea Setini. Molecular and cellular responses to short exposure to bisphenols A, F, and S and eluates of microplastics in C. elegans. Environmental science and pollution research international. 2021 Jan;28(1):805-818

    Expand section icon Mesh Tags

    Expand section icon Substances


    PMID: 32820443

    View Full Text