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

被引:41
作者
Ulhaq, Zulvikar Syambani [1 ,2 ]
Tse, William Ka Fai [1 ]
机构
[1] Kyushu Univ, Fac Agr, Ctr Promot Int Educ & Res, Lab Dev Disorders & Toxicol, Fukuoka 8190395, Japan
[2] Natl Res & Innovat Agcy, Res Ctr Preclin & Clin Med, Cibinong 16911, Indonesia
基金
日本学术振兴会;
关键词
Cell cycle; Embryogenesis; Environmental pollutant; Oxidative stress; PFAS; PERFLUOROOCTANE SULFONATE; POLYFLUOROALKYL SUBSTANCES; PERFLUOROALKYL SUBSTANCES; PERFLUORINATED COMPOUNDS; LIPID-PEROXIDATION; EXPOSURE; ELIMINATION; BINDING; WATER; PFOS;
D O I
10.1016/j.jhazmat.2023.131722
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
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
引用
收藏
页数:16
相关论文
共 50 条
[21]   Evidence for neurotoxicity and oxidative stress in zebrafish embryos/larvae treated with HFPO-DA ammonium salt (GenX) [J].
Ivantsova, Emma ;
Lopez-Scarim, Victoria ;
Sultan, Amany ;
English, Cole ;
Biju, Angel ;
Souders II, Christopher L. ;
Padillo-Anthemides, Natalia E. ;
Konig, Isaac ;
Martyniuk, Christopher J. .
ENVIRONMENTAL TOXICOLOGY AND PHARMACOLOGY, 2023, 104
[22]   Genipin induces developmental toxicity through oxidative stress and apoptosis in zebrafish [J].
Xia, Zhong-Shang ;
Hao, Er-Wei ;
Wei, Yan-ting ;
Hou, Xiao-Tao ;
Chen, Zhang-mei ;
Wei, Man ;
Du, Zheng-Cai ;
Deng, Jia-Gang .
COMPARATIVE BIOCHEMISTRY AND PHYSIOLOGY C-TOXICOLOGY & PHARMACOLOGY, 2021, 241
[23]   Environmental relevant concentrations of triclosan affected developmental toxicity, oxidative stress, and apoptosis in zebrafish embryos [J].
Liu, Fei ;
Zhang, Ying ;
Wang, Fan .
ENVIRONMENTAL TOXICOLOGY, 2022, 37 (04) :848-857
[24]   Isoniazid causes heart looping disorder in zebrafish embryos by the induction of oxidative stress [J].
Ni, Jie ;
Wang, Hongye ;
Wei, Xiyi ;
Shen, Kangjie ;
Sha, Yeqin ;
Dong, Yuxiang ;
Shu, Yimei ;
Wan, Xiaojie ;
Cheng, Jingwen ;
Wang, Fang ;
Liu, Yihai .
BMC PHARMACOLOGY & TOXICOLOGY, 2020, 21 (01)
[25]   Isoniazid causes heart looping disorder in zebrafish embryos by the induction of oxidative stress [J].
Jie Ni ;
Hongye Wang ;
Xiyi Wei ;
Kangjie Shen ;
Yeqin Sha ;
Yuxiang Dong ;
Yimei Shu ;
Xiaojie Wan ;
Jingwen Cheng ;
Fang Wang ;
Yihai Liu .
BMC Pharmacology and Toxicology, 21
[26]   Haloxyfop-P-methyl induces developmental defects in zebrafish embryos through oxidative stress and anti-vasculogenesis [J].
Park, Sunwoo ;
Lee, Jin-Young ;
Park, Hahyun ;
Song, Gwonhwa ;
Lim, Whasun .
COMPARATIVE BIOCHEMISTRY AND PHYSIOLOGY C-TOXICOLOGY & PHARMACOLOGY, 2020, 233
[27]   Developmental Toxicity of Diethylnitrosamine in Zebrafish Embryos/Juveniles Related to Excessive Oxidative Stress [J].
Danping Huang ;
Hanmin Li ;
Qidi He ;
Weiqu Yuan ;
Zuanguang Chen ;
Hongzhi Yang .
Water, Air, & Soil Pollution, 2018, 229
[28]   Clozapine Induced Developmental and Cardiac Toxicity on Zebrafish Embryos by Elevating Oxidative Stress [J].
Feng Zhang ;
Liwen Han ;
Jiazhen Wang ;
Minglei Shu ;
Kechun Liu ;
Yun Zhang ;
ChungDer Hsiao ;
Qingping Tian ;
Qiuxia He .
Cardiovascular Toxicology, 2021, 21 :399-409
[29]   Lenvatinib induces cardiac developmental toxicity in zebrafish embryos through regulation of Notch mediated-oxidative stress generation [J].
Liu, Jieping ;
Huang, Ling ;
Wan, Mengqi ;
Chen, Guilan ;
Su, Meile ;
Han, Fang ;
Liu, Fasheng ;
Xiong, Guanghua ;
Liao, Xinjun ;
Lu, Huiqiang ;
Li, Wanbo ;
Cao, Zigang .
ENVIRONMENTAL TOXICOLOGY, 2022, 37 (06) :1310-1320
[30]   Clozapine Induced Developmental and Cardiac Toxicity on Zebrafish Embryos by Elevating Oxidative Stress [J].
Zhang, Feng ;
Han, Liwen ;
Wang, Jiazhen ;
Shu, Minglei ;
Liu, Kechun ;
Zhang, Yun ;
Hsiao, ChungDer ;
Tian, Qingping ;
He, Qiuxia .
CARDIOVASCULAR TOXICOLOGY, 2021, 21 (05) :399-409