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    Por favor, use este identificador para citar o enlazar este ítem: http://hdl.handle.net/10259/9295

    Título
    Are the BPA analogues an alternative to classical BPA? Comparison between 2D and alternative 3D in vitro neuron model to assess cytotoxic and genotoxic effects
    Autor
    Sendra Vega, MartaAutoridad UBU Orcid
    Cavia Saiz, MónicaAutoridad UBU Orcid
    Muñiz Rodríguez, PilarAutoridad UBU Orcid
    Publicado en
    Toxicology. 2024, V. 502, 153715
    Editorial
    Elsevier
    Fecha de publicación
    2024-02
    ISSN
    0300-483X
    DOI
    10.1016/j.tox.2023.153715
    Résumé
    BPA is used in a wide range of consumer products with very concern toxicological properties. The European Union has restricted its use to protect human health. Industry has substituted BPA by BPA analogues. However, there is a lack of knowledge about their impacts. In this work, BPA and 5 BPA analogues (BPS, BPAP, BPAF, BPFL and BPC) have been studied in classical SH-SY5Y and the alternative 3D in vitro models after 24 and 96 h of exposure. Cell viability, percentage of ROS, cell cycle phases as well as the morphology of the spheroids were measured. The 2D model was more sensitive than the 3D models with differences in cell viability higher than 60% after 24 h of exposure, and different mechanisms of ROS production. After chronic exposure, both models were more affected in comparison to the 24 h exposure. After a recovery time (96 h), the spheroids exposed to 2.5–40 µM were able to recover cell viability and the morphology. Among the BPs tested, BPFL>BPAF>BPAP and >BPC revealed higher toxicological effects, while BPS was the only one with lower effects than BPA. To conclude, the SH-SY5Y 3D model is a suitable candidate to perform more reliable in vitro neurotoxicity tests.
    Palabras clave
    Toxicology
    BPA analogues
    Recovery assays
    SH-SY5Y 3D model
    Alternative in vitro model
    Materia
    Bioquímica
    Biochemistry
    Biología molecular
    Molecular biology
    URI
    http://hdl.handle.net/10259/9295
    Versión del editor
    https://doi.org/10.1016/j.tox.2023.153715
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    Sendra-toxicology_2024.pdf
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