Amstutz V H, Cengo A, Gehres F, Sijm D T H M, Vrolijk M F
Department of Pharmacology and Toxicology, Maastricht University, 6229 ER Maastricht, the Netherlands.
Department of Pharmacology and Toxicology, Maastricht University, 6229 ER Maastricht, the Netherlands.
Toxicology. 2022 Oct;480:153312. doi: 10.1016/j.tox.2022.153312. Epub 2022 Sep 6.
Per- and polyfluoroalkyl substances (PFAS) are a family of man-made chemicals with currently over 4'700 compounds identified. While toxicological data are available for some of the legacy PFAS, such as PFOA and PFOS, a knowledge gap remains concerning both emerging and legacy PFAS' toxicity due to the diversity of the PFAS. Therefore, a better understanding of the PFAS structure-activity relationship may prove helpful. The present study investigated a potential structure-activity relationship between PFAS and hepatotoxicity. As such, the effects of thirteen PFAS with varying carbon chain-length and functional head-groups (in a concentration range of 0-800 µM) on the cell viability of HepG2 cells and intracellular reactive oxygen species formation have been tested using the MTT and DCFH assay, respectively. The exposure times were either 3 or 24 h. In addition, intracellular PFAS levels were determined in HepG2 after 24 h exposure. The present study demonstrated that the cytotoxicity of PFAS is dependent on their chain-length as cell viability decreased with increasing chain-length at both exposure times. Calculated Relative Potency Factors (RPF), based on the TC values, were used for a tentative ranking of PFAS regarding their hepatotoxicity: PFNA ˃ PFDA ˃ PFOS ≥ PFOA ˃ PFHxS ˃ PFBS ˃˃ PFHpA = PFHxA = PFBA = PFPrA = 6:2 FTOH = 4:2 = FTOH = 3:1 FTOH. Similar results were observed regarding intracellular reactive oxygen species generation at both exposure times, with a tentative ranking of: PFNA ˃ PFOS ˃ PFOA ≥ PFDA ˃ PFHxS ˃ PFBS ˃ PFBA ˃ PFHpA ≥ PFHxA ˃ PFPrA ˃ 6:2 FTOH = 4:2 FTOH = 3:1 FTOH. Moreover, a concentration-dependent reactive oxygen species generation has been observed for all PFSAs and PFCAs, but not for the FTOHs. In conclusion, the carbon chain-length and functional head-group of a PFAS determine their in vitro toxicity for the two toxicological endpoints assessed in the present study. Moreover, no effects were observed for the tested FTOHs. As such, the present study established a potential structure-activity relationship that opens the possibility of developing a predictive model to help with the risk assessment of PFAS in the future.
全氟和多氟烷基物质(PFAS)是一类人造化学品,目前已鉴定出超过4700种化合物。虽然一些传统PFAS(如全氟辛酸和全氟辛烷磺酸)已有毒理学数据,但由于PFAS种类繁多,新型和传统PFAS的毒性方面仍存在知识空白。因此,更好地理解PFAS的构效关系可能会有所帮助。本研究调查了PFAS与肝毒性之间潜在的构效关系。为此,分别使用MTT和DCFH检测法测试了13种具有不同碳链长度和官能团头基(浓度范围为0 - 800µM)的PFAS对HepG2细胞活力和细胞内活性氧生成的影响。暴露时间为3小时或24小时。此外,在暴露24小时后测定了HepG2细胞内的PFAS水平。本研究表明,PFAS的细胞毒性取决于其链长,在两个暴露时间下,细胞活力均随链长增加而降低。基于毒性阈值(TC)值计算的相对 potency 因子(RPF)用于对PFAS的肝毒性进行初步排序:全氟壬酸>全氟癸酸>全氟辛烷磺酸≥全氟辛酸>全氟己烷磺酸>全氟丁烷磺酸>>全氟庚酸 = 全氟己酸 = 全氟丁酸 = 全氟丙酸 = 6:2氟调醇 = 4:2氟调醇 = 3:1氟调醇。在两个暴露时间下,关于细胞内活性氧生成也观察到了类似结果,初步排序为:全氟壬酸>全氟辛烷磺酸>全氟辛酸≥全氟癸酸>全氟己烷磺酸>全氟丁烷磺酸>全氟丁酸>全氟庚酸≥全氟己酸>全氟丙酸>6:2氟调醇 = 4:2氟调醇 = 3:1氟调醇。此外,观察到所有全氟磺酸和全氟羧酸均有浓度依赖性的活性氧生成,但氟调醇没有。总之,PFAS的碳链长度和官能团头基决定了它们在本研究评估的两个毒理学终点的体外毒性。此外,在所测试的氟调醇中未观察到影响。因此,本研究建立了一种潜在的构效关系,为未来开发预测模型以帮助进行PFAS风险评估开辟了可能性。