Center for Water and Health, Key Laboratory of the Public Health Safety, Ministry of Education, Department of Environmental Health, School of Public Health, Fudan University Shanghai, 200032, China.
Wolfson College, Oxford University, Oxford OX2 6UD, United Kingdom.
Water Res. 2024 Sep 1;261:122008. doi: 10.1016/j.watres.2024.122008. Epub 2024 Jun 27.
Non-alcoholic fatty liver disease (NAFLD) is a metabolic disorder characterized by abnormal lipid deposition, with oxidative stress being a risk factor in its onset and progression. Haloacetamides (HAcAms), as unregulated disinfection by-products in drinking water, may alter the incidence and severity of NAFLD through the production of oxidative stress. We explored whether HAcAms at 1, 10, and 100-fold concentrations in Shanghai drinking water perturbed lipid metabolism in normal human liver LO-2 cells. CRISPR/Cas9 was used to construct a LO-2 line with stable NRF2 knock-down (NRF2-KD) to investigate the mechanism underlying abnormal lipid accumulation and hepatocyte damage caused by mixed exposure to HAcAms. At 100-fold real-world concentration, HAcAms caused lipid deposition and increased triglyceride accumulation in LO-2 cells, consistent with altered de novo lipogenesis. Differences in responses to HAcAms in normal and NRF2-KD LO-2 cells indicated that HAcAms caused hepatocyte lipid deposition and triglyceride accumulation by activation of the NRF2/PPARγ pathway and aggravated liver cell toxicity by inducing ferroptosis. These results indicate that HAcAms are important risk factors for NAFLD. Further observations and verifications of the effect of HAcAms on NAFLD in the population are warranted in the future.
非酒精性脂肪性肝病(NAFLD)是一种代谢紊乱疾病,其特征是脂质沉积异常,氧化应激是其发病和进展的危险因素。卤乙酰胺(HAcAms)作为饮用水中不受管制的消毒副产物,可能通过产生氧化应激来改变 NAFLD 的发病率和严重程度。我们探讨了上海饮用水中 HAcAms 的浓度分别为 1 倍、10 倍和 100 倍时是否会干扰正常人肝 LO-2 细胞的脂质代谢。使用 CRISPR/Cas9 构建了 LO-2 细胞中 NRF2 稳定敲低(NRF2-KD)的系,以研究混合暴露于 HAcAms 引起异常脂质积累和肝细胞损伤的机制。在 100 倍实际浓度下,HAcAms 导致 LO-2 细胞内脂质沉积和甘油三酯积累增加,与从头合成脂质代谢改变一致。正常 LO-2 细胞和 NRF2-KD LO-2 细胞对 HAcAms 反应的差异表明,HAcAms 通过激活 NRF2/PPARγ 通路导致肝细胞脂质沉积和甘油三酯积累,并通过诱导铁死亡加重肝毒性。这些结果表明 HAcAms 是非酒精性脂肪性肝病的重要危险因素。未来有必要进一步观察和验证 HAcAms 对人群中 NAFLD 的影响。