Department of Bioanalytical Ecotoxicology, Chemicals in the Environment Research Section, Helmholtz-Centre for Environmental Research-UFZ, Leipzig, Germany.
Center for Computational Toxicology and Exposure, Office of Research and Development, US Environmental Protection Agency, Research Triangle Park, North Carolina, USA.
Environ Health Perspect. 2024 Jul;132(7):77007. doi: 10.1289/EHP13667. Epub 2024 Jul 24.
Per- and polyfluoroalkyl Substances (PFAS) are synthetic chemicals widely detected in humans and the environment. Exposure to perfluorooctanesulfonic acid (PFOS) or perfluorohexanesulfonic acid (PFHxS) was previously shown to cause dark-phase hyperactivity in larval zebrafish.
The objective of this study was to elucidate the mechanism by which PFOS or PFHxS exposure caused hyperactivity in larval zebrafish.
Swimming behavior was assessed in 5-d postfertilization (dpf) larvae following developmental (1-4 dpf) or acute (5 dpf) exposure to PFOS, PFHxS, or 0.4% dimethyl sulfoxide (DMSO). After developmental exposure and chemical washout at 4 dpf, behavior was also assessed at 5-8 dpf. RNA sequencing was used to identify differences in global gene expression to perform transcriptomic benchmark concentration-response () modeling, and predict upstream regulators in PFOS- or PFHxS-exposed larvae. CRISPR/Cas9-based gene editing was used to knockdown peroxisome proliferator-activated receptors (ppars) , , or at day 0. Knockdown crispants were exposed to PFOS or 0.4% DMSO from 1-4 dpf and behavior was assessed at 5 dpf. Coexposure with the ppard antagonist GSK3787 and PFOS was also performed.
Transient dark-phase hyperactivity occurred following developmental or acute exposure to PFOS or PFHxS, relative to the DMSO control. In contrast, visual startle response (VSR) hyperactivity only occurred following developmental exposure and was irreversible up to 8 dpf. Similar global transcriptomic profiles, estimates, and enriched functions were observed in PFOS- and PFHxS-exposed larvae, and ppars were identified as putative upstream regulators. Knockdown of , but not or , blunted PFOS-dependent VSR hyperactivity to control levels. This finding was confirmed via antagonism of in PFOS-exposed larvae.
This work identifies a novel adverse outcome pathway for VSR hyperactivity in larval zebrafish. We demonstrate that developmental, but not acute, exposure to PFOS triggered persistent VSR hyperactivity that required function. https://doi.org/10.1289/EHP13667.
全氟和多氟烷基物质(PFAS)是广泛存在于人类和环境中的合成化学品。先前的研究表明,接触过氟辛酸(PFOS)或全氟己烷磺酸(PFHxS)会导致幼斑马鱼在暗期过度活跃。
本研究旨在阐明 PFOS 或 PFHxS 暴露导致幼斑马鱼过度活跃的机制。
在 5 天孵化后(dpf)幼鱼中,通过发育(1-4 dpf)或急性(5 dpf)暴露于 PFOS、PFHxS 或 0.4%二甲基亚砜(DMSO),评估游泳行为。在 4 dpf 时进行发育暴露和化学清洗后,还在 5-8 dpf 时评估行为。使用 RNA 测序来识别全局基因表达的差异,进行转录组基准浓度反应()建模,并预测 PFOS 或 PFHxS 暴露幼鱼中的上游调节剂。使用 CRISPR/Cas9 基因编辑在第 0 天敲低过氧化物酶体增殖物激活受体(ppars)、或。敲低crisprants 从 1-4 dpf 暴露于 PFOS 或 0.4% DMSO,并在 5 dpf 时评估行为。还进行了与 ppard 拮抗剂 GSK3787 和 PFOS 的共暴露。
与 DMSO 对照组相比,在发育或急性暴露于 PFOS 或 PFHxS 后,幼鱼在暗期出现短暂的过度活跃。相比之下,只有在发育暴露后才会出现视觉惊跳反应(VSR)过度活跃,并且在 8 dpf 之前是不可逆的。在 PFOS 和 PFHxS 暴露的幼鱼中观察到相似的全局转录组图谱、估计值和富集功能,并且鉴定出 ppars 为假定的上游调节剂。敲低,但不是 或 ,可使 PFOS 依赖性 VSR 过度活跃恢复至对照水平。这一发现通过在 PFOS 暴露的幼鱼中拮抗 得到了证实。
本工作确定了幼斑马鱼 VSR 过度活跃的新的不良结局途径。我们证明,发育暴露而不是急性暴露于 PFOS 会引发持久的 VSR 过度活跃,这需要 功能。https://doi.org/10.1289/EHP13667.