Next generation risk assessment of hair dye HC yellow no. 13: Ensuring protection from liver steatogenic effects

IF 3 4区 医学 Q1 MEDICINE, LEGAL
Sara Sepehri, Dinja De Win, Anja Heymans, Freddy Van Goethem, Robim M. Rodrigues, Vera Rogiers, Tamara Vanhaecke
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引用次数: 0

Abstract

This study employs animal-free Next Generation Risk Assessment (NGRA) principles to evaluate the safety of repeated dermal exposure to 2.5% (w/w) HC Yellow No. 13 (HCY13) hair dye. As multiple in silico tools consistently flagged hepatotoxic potential, likely due to HCY13's trifluoromethyl group, which is known to interfere with hepatic lipid metabolism, liver steatosis was chosen as the primary mode of action for evaluation. AOP-guided in vitro tests were conducted, exposing human stem cell-derived hepatic cells to varying HCY13 concentrations over 72 h. The expression of 11 lipid metabolism-related marker genes (AHR, PPARA, LXRA, APOB, ACOX1, CPT1A, FASN, SCD1, DGAT2, CD36, and PPARG) and triglyceride accumulation, a phenotypic hallmark of steatosis, were measured. PROAST software was used to calculate in vitro Points of Departure (PoDNAM) for each biomarker. Using GastroPlus 9.9, physiologically-based pharmacokinetic (PBPK) models estimated internal liver concentrations (Cmax liver) of HCY13, ranging from 4 to 20 pM. All PoDNAM values significantly exceeded the predicted Cmax liver, indicating that HCY13 at 2.5% (w/w) is unlikely to induce liver steatosis under the assumed conditions. This research demonstrates the utility of NGRA, integrating AOP-based in vitro assays and computational models to protect human health and support regulatory decision-making without animal testing.
染发剂HC黄13号的新一代风险评估:确保保护免受肝脏脂肪的影响。
本研究采用无动物的下一代风险评估(NGRA)原则来评估皮肤反复暴露于2.5% (w/w) HC黄13 (HCY13)染发剂的安全性。由于多种硅工具一致标记出肝毒性潜力,可能是由于HCY13的三氟甲基,已知会干扰肝脏脂质代谢,因此选择肝脂肪变性作为评估的主要作用模式。在aop引导下进行了体外试验,将人干细胞来源的肝细胞暴露在不同浓度的HCY13中72小时。测量了11种脂质代谢相关标记基因(AHR、PPARA、LXRA、APOB、ACOX1、CPT1A、FASN、SCD1、DGAT2、CD36和PPARG)的表达和甘油三酯积累(脂肪变性的表型标志)。使用PROAST软件计算每个生物标志物的体外出发点(PoDNAM)。使用GastroPlus 9.9,基于生理的药代动力学(PBPK)模型估计HCY13的肝脏内部浓度(Cmax肝脏),范围从4到20 pM。所有PoDNAM值均显著超过预测的Cmax肝脏,表明2.5% (w/w)的HCY13不太可能在假设条件下诱导肝脏脂肪变性。本研究展示了NGRA的实用性,整合了基于aop的体外分析和计算模型,以保护人类健康并支持监管决策,而无需动物试验。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
6.70
自引率
8.80%
发文量
147
审稿时长
58 days
期刊介绍: Regulatory Toxicology and Pharmacology publishes peer reviewed articles that involve the generation, evaluation, and interpretation of experimental animal and human data that are of direct importance and relevance for regulatory authorities with respect to toxicological and pharmacological regulations in society. All peer-reviewed articles that are published should be devoted to improve the protection of human health and environment. Reviews and discussions are welcomed that address legal and/or regulatory decisions with respect to risk assessment and management of toxicological and pharmacological compounds on a scientific basis. It addresses an international readership of scientists, risk assessors and managers, and other professionals active in the field of human and environmental health. Types of peer-reviewed articles published: -Original research articles of relevance for regulatory aspects covering aspects including, but not limited to: 1.Factors influencing human sensitivity 2.Exposure science related to risk assessment 3.Alternative toxicological test methods 4.Frameworks for evaluation and integration of data in regulatory evaluations 5.Harmonization across regulatory agencies 6.Read-across methods and evaluations -Contemporary Reviews on policy related Research issues -Letters to the Editor -Guest Editorials (by Invitation)
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