妊娠期和哺乳期接触全氟辛烷磺酸、全氟辛烷磺酸和全氟己烷磺酸混合物会改变 CD-1 小鼠后代的肝脏蛋白质组

Toxics Pub Date : 2024-05-09 DOI:10.3390/toxics12050348
Emily Kaye, E. Marques, Juliana Agudelo Areiza, Seyed Mohamad Sadegh Modaresi, Angela Slitt
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摘要

全氟烷基物质(PFASs)是一种持久性人造化学物质,被认为是新出现的污染物,其中全氟辛酸(PFOA)、全氟辛烷磺酸(PFOS)和全氟己烷磺酸(PFHxS)与肝毒性和脂肪变性有关。全氟辛烷磺酸、全氟辛烷磺酸和全氟己烷磺酸可通过胎盘和哺乳期转移,导致全氟辛烷磺酸、全氟辛烷磺酸和全氟己烷磺酸分布到新生儿肝脏。此外,妊娠母体暴露于全氟辛烷磺酸混合物,再加上高脂肪饮食,会增加新生儿在出生后第 21 天的肝脏脂肪变性,但其机制尚未阐明。假设妊娠期/哺乳期接触全氟辛烷磺酸会改变幼鼠肝脏蛋白质组和生化/信号通路。给定时妊娠的 CD-1 母鼠喂食标准饲料或 60% 千卡高脂肪饮食。从 GD1 到 PND20,通过口服灌胃给母鼠服用载体(0.5% 吐温 20)、单剂量 PFOA、PFOS、PFHxS(1 毫克/千克)或混合物(各 1 毫克/千克,合计 3 毫克/千克)。收集 PND21 后代的肝脏并进行 SWATH-MS 蛋白质组学分析。IPA 分析显示,PFAS 暴露改变了 PND21 肝脏中涉及肝损伤、异物和脂质调节的疾病和生物功能通路。这些途径包括脂质和脂肪酸的转运、储存、氧化和合成,以及异生物代谢和转运、肝损伤和炎症。这表明幼鼠肝脏蛋白质组会因母体暴露而发生改变,并使幼鼠容易出现代谢功能障碍。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Exposure to a PFOA, PFOS and PFHxS Mixture during Gestation and Lactation Alters the Liver Proteome in Offspring of CD-1 Mice
Perfluroalkyl substances (PFASs) are persistent man-made chemicals considered to be emerging pollutants, with Perfluorooctanoic acid (PFOA), Perfluorooctanesulfonic acid (PFOS), and Perfluorohexanesulphonic acid (PFHxS) being linked to hepatotoxicity and steatosis. PFOA, PFOS, and PFHxS can undergo placental and lactational transfer, which results in PFOA, PFOS, and PFHxS distribution to the neonatal liver. Moreover, in pregnant dams, exposure to a PFAS mixture, in combination with a high fat diet, increased hepatic steatosis in offspring at postnatal day 21, but the mechanisms have not been elucidated. It was hypothesized that gestational/lactational PFAS exposure would alter the pup liver proteome and biochemical/signaling pathways. Timed-pregnant CD-1 dams were fed a standard chow or 60% kcal high-fat diet. From GD1 until PND20, dams were dosed via oral gavage with vehicle (0.5% Tween 20), individual doses of PFOA, PFOS, PFHxS at 1 mg/kg, or a mixture (1 mg/kg each, totaling 3 mg/kg). Livers were collected from PND21 offspring and SWATH-MS proteomics was performed. IPA analysis revealed PFAS exposure modified disease and biological function pathways involved in liver damage, xenobiotics, and lipid regulation in the PND21 liver. These pathways included lipid and fatty acid transport, storage, oxidation, and synthesis, as well as xenobiotic metabolism and transport, and liver damage and inflammation. This indicates the pup liver proteome is altered via maternal exposure and predisposes the pup to metabolic dysfunctions.
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