Evaluation of Per- and Polyfluoroalkyl Substances (PFAS) Toxicity Testing for Developmental Neurotoxicity.

Kelly E Carstens, Theresa Freudenrich, Kathleen Wallace, Seline Choo, Amy Carpenter, Marci Smeltz, Matthew S Clifton, W Matthew Henderson, Ann M Richard, Grace Patlewicz, Barbara A Wetmore, Katie Paul Friedman, Timothy Shafer

Journal: Chemical research in toxicology 2023;36(3):402-419

PMID: 36821828

Abstract

Per- and polyfluoroalkyl substances (PFAS) are a diverse set of commercial chemicals widely detected in humans and the environment. However, only a limited number of PFAS are associated with epidemiological or experimental data for hazard identification. To provide developmental neurotoxicity (DNT) hazard information, the work herein employed DNT new approach methods (NAMs) to generate screening data for a set of 160 PFAS. The DNT NAMs battery was comprised of the microelectrode array neuronal network formation assay (NFA) and high-content imaging (HCI) assays to evaluate proliferation, apoptosis, and neurite outgrowth. The majority of PFAS (118/160) were inactive or equivocal in the DNT NAMs, leaving 42 active PFAS that decreased measures of neural network connectivity and neurite length. Analytical quality control indicated 43/118 inactive PFAS samples and 10/42 active PFAS samples were degraded; as such, careful interpretation is required as some negatives may have been due to loss of the parent PFAS, and some actives may have resulted from a mixture of parent and/or degradants of PFAS. PFAS containing a perfluorinated carbon (C) chain length ≥8, a high C:fluorine ratio, or a carboxylic acid moiety were more likely to be bioactive in the DNT NAMs. Of the PFAS positives in DNT NAMs, 85% were also active in other EPA ToxCast assays, whereas 79% of PFAS inactives in the DNT NAMs were active in other assays. These data demonstrate that a subset of PFAS perturb neurodevelopmental processes and suggest focusing future studies of DNT on PFAS with certain structural feature descriptors.

Address: Center for Computational Toxicology and Exposure, ORD, US EPA, Research Triangle Park, North Carolina 27711, United States.; Oak Ridge Institute for Science and Education (ORISE), Oak Ridge, Tennessee 37830, United States.; Center for Environmental Measurement and Modeling, ORD, US EPA, Research Triangle Park, North Carolina 27711, United States.
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