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    Por favor, use este identificador para citar o enlazar este ítem: http://hdl.handle.net/10259/8561

    Título
    NMR-Based Metabolomics Approach to Explore Brain Metabolic Changes Induced by Prenatal Exposure to Autism-Inducing Chemicals
    Autor
    Abreu, Ana Cristina
    Morales Navas, MiguelUBU authority Orcid
    Pérez Fernández, Cristian AntonioUBU authority Orcid
    Sánchez Santed, Fernando
    Fernández, Ignacio
    Publicado en
    ACS Chemical Biology. 2021, V. 16, n. 4, p. 753-765
    Editorial
    American Chemical Society
    Fecha de publicación
    2021
    ISSN
    1554-8929
    DOI
    10.1021/ACSCHEMBIO.1C00053
    Abstract
    NMR offers the unique potential to holistically screen hundreds of metabolites and has already proved to be a powerful technique able to provide a global picture of a wide range of metabolic processes underlying complex and multifactorial diseases, such as neurodegenerative and neurodevelopmental diseases. The aim of this study was to apply an NMR-based metabolomics approach to explore brain metabolic changes in both male and female rats induced by prenatal exposure to two chemicals associated with autism disorders—the organophosphorus pesticide chlorpyrifos (CPF) and the antiepileptic drug valproic acid (VPA)—at different postnatal ages. Depending on the age and on the brain region (hippocampus and cerebellum), several metabolites were shown to be significantly affected by exposure to both compounds. The evaluation of the spectral profiles revealed that the nervous-system-specific metabolite N-acetylaspartate (NAA), amino acid neurotransmitters (e.g., glutamate, glutamine, GABA, glycine), pyroglutamic acid, unsaturated fatty acids, and choline-based compounds are discriminant biomarkers. Additionally, metabolic changes varied as a function of age, but importantly not of sex.
    Materia
    Fisiología
    Physiology
    Química física
    Chemistry, Physical and theoretical
    Psicología
    Psychology
    Salud
    Health
    URI
    http://hdl.handle.net/10259/8561
    Versión del editor
    https://doi.org/10.1021/ACSCHEMBIO.1C00053
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