Abudayyak Mahmoud, Öztaş Ezgi, Özhan Gül
Department of Pharmaceutical Toxicology, Faculty of Pharmacy, Karadeniz Technical University, Trabzon, Turkey.
Department of Pharmaceutical Toxicology, Faculty of Pharmacy, Istanbul University, Istanbul, Turkey.
J Health Pollut. 2021 Aug 17;11(31):210909. doi: 10.5696/2156-9614-11.31.210909. eCollection 2021 Sep.
Perfluorooctanoic acid (PFOA) is used in different industrial and commercial products. Research shows the presence of PFOA in home dusts, tap and surface water, and in biological samples. The International Agency for Research on Cancer (IARC) has classified PFOA as a possible carcinogen for humans. The liver is thought to be a target organ of PFOA accumulation and toxicity.
Some studies have found toxic effects on the liver and related mechanisms; however, more studies are needed to better understand PFOA - induced hepatotoxicity.
In the present study, a human hepatocarcinoma cell line was exposed to PFOA for 24 hours and cell viability, apoptosis, the oxidative system and immune response were evaluated.
While apoptosis was the main cell death pathway at low concentration (86.5%), the necrotic cell fraction increased with higher concentrations (46.7%). Significant changes in the reactive oxygen species (5.3-folds) glutathione (GSH) (1.7-folds) and catalase (CAT) (1.4-folds) levels were observed, as well as changes to interleukin-6 (≤1.8-fold) and interleukin-8 levels (35-40%).
In light of the data, PFOA is potentially hepatotoxic through the investigated pathways. The results represent a background for future in vivo mechanistic studies.
The authors declare no competing financial interests.
全氟辛酸(PFOA)用于不同的工业和商业产品中。研究表明,家庭灰尘、自来水和地表水以及生物样本中均存在PFOA。国际癌症研究机构(IARC)已将PFOA归类为对人类可能的致癌物。肝脏被认为是PFOA蓄积和毒性的靶器官。
一些研究已发现PFOA对肝脏的毒性作用及其相关机制;然而,需要更多研究以更好地了解PFOA诱导的肝毒性。
在本研究中,将一种人肝癌细胞系暴露于PFOA 24小时,并评估细胞活力、凋亡、氧化系统和免疫反应。
低浓度时凋亡是主要的细胞死亡途径(86.5%),而坏死细胞比例随浓度升高而增加(46.7%)。观察到活性氧(5.3倍)、谷胱甘肽(GSH)(1.7倍)和过氧化氢酶(CAT)(1.4倍)水平有显著变化,白细胞介素-6(≤1.8倍)和白细胞介素-8水平也有变化(35 - 40%)。
根据这些数据,PFOA可能通过所研究的途径具有肝毒性。这些结果为未来的体内机制研究提供了背景资料。
作者声明不存在相互竞争的财务利益。