Perfluorohexanesulfonic acid (PFHxS) induces oxidative stress and causes developmental toxicities in zebrafish embryos

Perfluorohexanesulfonic acid (PFHxS) is a short-chain perfluoroalkyl substance widely used to replace the banned perfluorooctanesulfonic acid (PFOS) in different industrial and household products. It has currently been identified in the environment and human bodies; nonetheless, the possible toxicities are not well-known. Zebrafish have been used as a toxicant screening model due to their fast and transparent developmental pro-cesses. In this study, zebrafish embryos were exposed to PFHxS for five days, and various experiments were performed to monitor the developmental and cellular processes. Liquid chromatography-mass spectrometry (LC/ MS) analysis confirmed that PFHxS was absorbed and accumulated in the zebrafish embryos. We reported that 2.5 mu M or higher PFHxS exposure induced phenotypic abnormalities, marked by developmental delay in the mid -hind brain boundary and yolk sac edema. Additionally, larvae exposed to PFHxS displayed facial malformation due to the reduction of neural crest cell expression. RNA sequencing analysis further identified 4643 differen-tiated expressed transcripts in 5 mu M PFHxS-exposed 5-days post fertilization (5-dpf) larvae. Bioinformatics analysis revealed that glucose metabolism, lipid metabolism, as well as oxidative stress were enriched in the PFHxS-exposed larvae. To validate these findings, a series of biological experiments were conducted. PFHxS exposure led to a nearly 4-fold increase in reactive oxygen species, possibly due to hyperglycemia and impaired glutathione balance. The Oil Red O' staining and qPCR analysis strengthens the notions that lipid metabolism was disrupted, leading to lipid accumulation, lipid peroxidation, and malondialdehyde formation. All these al-terations ultimately affected cell cycle events, resulting in S and G2/M cell cycle arrest. In conclusion, our study

Automated summary

In this study, zebrafish embryos were exposed to PFHxS and it was found that PFHxS accumulated in the embryos, leading to phenotypic abnormalities and disruption of cellular processes. Further analysis revealed that PFHxS affected glucose metabolism, lipid metabolism, and oxidative stress, resulting in increased reactive oxygen species, lipid accumulation, and cell cycle arrest. These findings highlight the potential toxicities of PFHxS.