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替代全氟辛烷磺酸全氟-(2,5,8-三甲基-3,6,9-三氧杂十二烷酸)(HFPO-TeA)的剂量反应、剂量测定和代谢评估。

Dose Response, Dosimetric, and Metabolic Evaluations of Replacement PFAS Perfluoro-(2,5,8-trimethyl-3,6,9-trioxadodecanoic) Acid (HFPO-TeA).

作者信息

Renyer Aero, Ravindra Krishna, Wetmore Barbara A, Ford Jermaine L, DeVito Michael, Hughes Michael F, Wehmas Leah C, MacMillan Denise K

机构信息

Oak Ridge Institute for Science and Education (ORISE), Oak Ridge, TN 37830, USA.

Oak Ridge Associated Universities (ORAU), Oak Ridge, TN 37830, USA.

出版信息

Toxics. 2023 Nov 22;11(12):951. doi: 10.3390/toxics11120951.

Abstract

Few studies are available on the environmental and toxicological effects of perfluoroalkyl ether carboxylic acids (PFECAs), such as GenX, which are replacing legacy PFAS in manufacturing processes. To collect initial data on the toxicity and toxicokinetics of a longer-chain PFECA, male and female Sprague Dawley rats were exposed to perfluoro-(2,5,8-trimethyl-3,6,9-trioxadodecanoic) acid (HFPO-TeA) by oral gavage for five days over multiple dose levels (0.3-335.2 mg/kg/day). Clinically, we observed mortality at doses >17 mg/kg/day and body weight changes at doses ≤17 mg/kg/day. For the 17 mg/kg/day dose level, T3 and T4 thyroid hormone concentrations were significantly decreased ( < 0.05) from controls and HFPO-TeA plasma concentrations were significantly different between sexes. Non-targeted analysis of plasma and in vitro hepatocyte assay extractions revealed the presence of another GenX oligomer, perfluoro-(2,5-dimethyl-3,6-dioxanonanoic) acid (HFPO-TA). In vitro to in vivo extrapolation (IVIVE) parameterized with in vitro toxicokinetic data predicted steady-state blood concentrations that were within seven-fold of those observed in the in vivo study, demonstrating reasonable predictivity. The evidence of thyroid hormone dysregulation, sex-based differences in clinical results and dosimetry, and IVIVE predictions presented here suggest that the replacement PFECA HFPO-TeA induces a complex and toxic exposure response in rodents.

摘要

关于全氟烷基醚羧酸(PFECA),如GenX,在制造过程中取代传统全氟辛烷磺酸的环境和毒理学影响的研究很少。为了收集关于一种较长链PFECA的毒性和毒代动力学的初始数据,将雄性和雌性斯普拉格-道利大鼠通过口服灌胃暴露于全氟-(2,5,8-三甲基-3,6,9-三氧杂十二烷酸)(HFPO-TeA),在多个剂量水平(0.3-335.2毫克/千克/天)下持续五天。临床上,我们观察到剂量>17毫克/千克/天时出现死亡,剂量≤17毫克/千克/天时出现体重变化。对于17毫克/千克/天的剂量水平,T3和T4甲状腺激素浓度与对照组相比显著降低(<0.05),且HFPO-TeA血浆浓度在两性之间存在显著差异。对血浆和体外肝细胞测定提取物的非靶向分析显示存在另一种GenX低聚物,全氟-(2,5-二甲基-3,6-二氧杂壬酸)(HFPO-TA)。用体外毒代动力学数据进行参数化的体外到体内外推(IVIVE)预测的稳态血药浓度在体内研究观察值的七倍以内,证明了合理的预测性。此处呈现的甲状腺激素失调、临床结果和剂量测定中的性别差异以及IVIVE预测的证据表明,替代PFECA HFPO-TeA在啮齿动物中引发了复杂的毒性暴露反应。

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