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Sulfonamide functional head on short-chain perfluorinated substance drives developmental toxicity.
Rericha, Yvonne; Cao, Dunping; Truong, Lisa; Simonich, Michael T; Field, Jennifer A; Tanguay, Robyn L.
  • Rericha Y; Department of Environmental and Molecular Toxicology, College of Agricultural Sciences, Oregon State University, Corvallis, OR 97333, USA.
  • Cao D; Sinnhuber Aquatic Research Laboratory, College of Agricultural Sciences, Oregon State University, Corvallis, OR 97333, USA.
  • Truong L; Department of Chemistry, College of Science, Oregon State University, Corvallis, OR 97333, USA.
  • Simonich MT; Department of Environmental and Molecular Toxicology, College of Agricultural Sciences, Oregon State University, Corvallis, OR 97333, USA.
  • Field JA; Sinnhuber Aquatic Research Laboratory, College of Agricultural Sciences, Oregon State University, Corvallis, OR 97333, USA.
  • Tanguay RL; Department of Environmental and Molecular Toxicology, College of Agricultural Sciences, Oregon State University, Corvallis, OR 97333, USA.
iScience ; 25(2): 103789, 2022 Feb 18.
Article en En | MEDLINE | ID: mdl-35146398
ABSTRACT
Per- and polyfluoroalkyl substances (PFAS) are ubiquitously detected in environmental and biological samples and cause adverse health effects. Studies have predominately focused on long-chain PFAS, with far fewer addressing short-chain alternatives. This study leveraged embryonic zebrafish to investigate developmental toxicity of a short-chain series perfluorobutane sulfonate (PFBS), perfluoropentanoic acid (PFPeA), perfluorobutane sulfonamide (FBSA), and 42 fluorotelomer sulfonic acid (42 FTS). Following static exposures at 8 h postfertilization (hpf) to each chemical (1-100 µM), morphological and behavioral endpoints were assessed at 24 and 120 hpf. Only FBSA induced abnormal morphology, while exposure to all chemicals caused aberrant larval behavior. RNA sequencing at 48 hpf following 47 µM exposures revealed only FBSA significantly disrupted normal gene expression. Measured tissue concentrations were FBSA > PFBS > 42 FTS > PFPeA. This study demonstrates functional head groups impact bioactivity and bioconcentration.
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