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全氟己烷磺酸(PFHxS)可诱导氧化应激,并导致斑马鱼胚胎的发育毒性。

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

机构信息

Laboratory of Developmental Disorders and Toxicology, Center for Promotion of International Education and Research, Faculty of Agriculture, Kyushu University, Fukuoka 8190395, Japan; Research Center for Pre-clinical and Clinical Medicine, National Research and Innovation Agency, Republic of Indonesia, Cibinong 16911, Indonesia.

Laboratory of Developmental Disorders and Toxicology, Center for Promotion of International Education and Research, Faculty of Agriculture, Kyushu University, Fukuoka 8190395, Japan.

出版信息

J Hazard Mater. 2023 Sep 5;457:131722. doi: 10.1016/j.jhazmat.2023.131722. Epub 2023 May 27.

Abstract

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 processes. 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 µM 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 differentiated expressed transcripts in 5 µM 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 alterations ultimately affected cell cycle events, resulting in S and G2/M cell cycle arrest. In conclusion, our study demonstrated that PFHxS could accumulate and induce various developmental toxicities in aquatic life, and such data might assist the government to accelerate the regulatory policy on PFHxS usage.

摘要

全氟己烷磺酸(PFHxS)是一种短链全氟烷基物质,广泛用于替代已被禁用的全氟辛烷磺酸(PFOS),应用于不同的工业和家用产品中。目前,它已经在环境和人体中被发现,但它的潜在毒性尚未得到充分了解。斑马鱼因其快速透明的发育过程而被用作毒物筛选模型。在这项研究中,斑马鱼胚胎在 PFHxS 中暴露了五天,并进行了各种实验来监测发育和细胞过程。液相色谱-质谱(LC/MS)分析证实 PFHxS 被吸收并在斑马鱼胚胎中积累。我们报告说,2.5 µM 或更高浓度的 PFHxS 暴露会导致表型异常,表现为中后脑边界发育延迟和卵黄囊水肿。此外,暴露于 PFHxS 的幼虫由于神经嵴细胞表达减少而出现面部畸形。RNA 测序分析进一步鉴定了 5 天受精后(5-dpf)幼虫在 5 µM PFHxS 暴露下有 4643 个分化表达的转录本。生物信息学分析表明,葡萄糖代谢、脂质代谢以及氧化应激在 PFHxS 暴露的幼虫中富集。为了验证这些发现,进行了一系列生物学实验。PFHxS 暴露导致活性氧增加近 4 倍,这可能是由于高血糖和谷胱甘肽平衡受损所致。油红 O 染色和 qPCR 分析进一步证实了脂质代谢被破坏,导致脂质积累、脂质过氧化和丙二醛形成。所有这些变化最终影响细胞周期事件,导致 S 和 G2/M 细胞周期停滞。总之,我们的研究表明 PFHxS 可以在水生生物中积累并引起各种发育毒性,这些数据可能有助于政府加速对 PFHxS 使用的监管政策。

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