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对暴露于短链全氟辛烷磺酸化合物HFPO-DA的小鼠肝脏转录组反应的评估。

Evaluation of Transcriptomic Responses in Livers of Mice Exposed to the Short-Chain PFAS Compound HFPO-DA.

作者信息

Heintz Melissa M, Chappell Grace A, Thompson Chad M, Haws Laurie C

机构信息

ToxStrategies, Inc, Asheville, NC, United States.

ToxStrategies, Inc, Katy, TX, United States.

出版信息

Front Toxicol. 2022 Jun 27;4:937168. doi: 10.3389/ftox.2022.937168. eCollection 2022.

Abstract

HFPO-DA (ammonium 2,3,3,3-tetrafluoro-2-(heptafluoropropoxy)-propanoate; CASRN 62037-80-3) is a component of the GenX technology platform used as a polymerization aid in the manufacture of some types of fluoropolymers. The liver is the primary target of toxicity for HFPO-DA in rodents and previous examination of hepatic transcriptomic responses in mice following oral exposure to HFPO-DA for 90 days showed induction of peroxisome proliferator-activated receptor signaling pathways, predominantly by PPARα, as well as increased gene expression of both peroxisomal and mitochondrial fatty acid metabolism. To further investigate the mechanism of liver toxicity, transcriptomic analysis was conducted on liver tissue from mice orally exposed to 0, 0.1, 0.5 or 5 mg/kg-bw/day HFPO-DA in a reproduction/developmental toxicity study. Hepatic gene expression changes demonstrated activation of the PPARα signaling pathway. Peroxisomal and mitochondrial fatty acid β-oxidation gene sets were enriched at lower HFPO-DA concentrations, and complement cascade, cell cycle and apoptosis related gene sets were enriched at higher HFPO-DA concentrations. These results support the reported histopathological findings in livers of mice from this study and indicate that the effects of HFPO-DA are mediated through rodent-specific PPARα signaling mechanisms regardless of reproductive status in mice.

摘要

全氟己基磺酸二胺盐(2,3,3,3-四氟-2-(七氟丙氧基)丙酸铵;化学物质登记号62037-80-3)是GenX技术平台的一种成分,在某些类型含氟聚合物的制造过程中用作聚合助剂。在啮齿动物中,肝脏是全氟己基磺酸二胺盐毒性的主要靶器官,先前对小鼠口服全氟己基磺酸二胺盐90天后肝脏转录组反应的研究表明,过氧化物酶体增殖物激活受体信号通路被诱导,主要是由PPARα介导,同时过氧化物酶体和线粒体脂肪酸代谢的基因表达也增加。为了进一步研究肝脏毒性的机制,在一项生殖/发育毒性研究中,对口服0、0.1、0.5或5毫克/千克体重/天全氟己基磺酸二胺盐的小鼠肝脏组织进行了转录组分析。肝脏基因表达变化表明PPARα信号通路被激活。在较低的全氟己基磺酸二胺盐浓度下,过氧化物酶体和线粒体脂肪酸β-氧化基因集富集,而在较高的全氟己基磺酸二胺盐浓度下,补体级联、细胞周期和凋亡相关基因集富集。这些结果支持了该研究中报告的小鼠肝脏组织病理学发现,并表明全氟己基磺酸二胺盐的作用是通过啮齿动物特异性的PPARα信号机制介导的,与小鼠的生殖状态无关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/33da/9271854/cb8e9defca03/ftox-04-937168-g001.jpg

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