State Key Laboratory of Pollution Control and Resource Reuse, School of Environment, Nanjing University, Nanjing, 210023, China.
State Key Laboratory of Pollution Control and Resource Reuse, School of Environment, Nanjing University, Nanjing, 210023, China.
Chemosphere. 2022 Dec;308(Pt 3):136543. doi: 10.1016/j.chemosphere.2022.136543. Epub 2022 Sep 20.
Organophosphorus flame retardants (OPFRs) are frequently detected in food and human samples, and epidemiological studies have found that human exposure to aryl-OPFRs (triphenyl phosphate, TPP) is associated with lipid metabolism. Although toxicity studies suggest a potential obesity risk from TPP exposure, the molecular mechanism remains unclear. This study investigated the subchronic dietary effects on mouse liver significantly changed proteins (SCPs) and elucidated the underlying molecular mechanisms of TPP with or without a high-fructose and high-fat (HFF) diet. Male C57BL/6J mice were exposed to low-dose TPP (corresponding to the oral reference dose, 10 μg/kg body weight (bw)/day) and high-dose TPP (1000 μg/kg bw/day) for 12 weeks. The results showed that exposure to TPP generated changes of liver function and organelle damage as well as increases in total cholesterol and triglyceride levels. TPP exposure at a low dose damaged the liver immune system via major histocompatibility complex-related proteins involved in antigen processing and presentation. TPP exposure at a high dose caused disorders of the biosynthesis of unsaturated fatty acids and steroid hormones, thereby inducing lipid accumulation in the liver. Although 10 μg/kg TPP did not cause serious lipid metabolism disorders in the liver, significant overexpression of fatty acid-binding protein 5, malic enzyme 1, and other related SCPs was observed, which led to disorders of cholesterol metabolism and lipogenesis to activate the proliferator-activated receptor signaling pathway and thus induced potential obesity risks. In addition, lipid metabolism disorders related to TPP were aggravated under the HFF diet, impairing liver mitochondrial and endoplasmic reticulum function in mice by altering the activity of cytochrome P450 enzyme subfamilies. These findings provide an in-depth understanding of the molecular toxicity mechanisms and health risks associated with subchronic exposure to TPP under different dietary regimes.
有机磷阻燃剂 (OPFRs) 经常在食品和人体样本中被检测到,流行病学研究发现人类接触芳香族 OPFRs(磷酸三苯酯,TPP)与脂质代谢有关。尽管毒性研究表明 TPP 暴露可能会增加肥胖的风险,但分子机制尚不清楚。本研究调查了亚慢性饮食对小鼠肝脏的影响,发现显著改变的蛋白质(SCPs),并阐明了 TPP 在高果糖和高脂肪(HFF)饮食存在或不存在的情况下的潜在分子机制。雄性 C57BL/6J 小鼠暴露于低剂量 TPP(相当于口服参考剂量,10μg/kg 体重/天)和高剂量 TPP(1000μg/kg bw/day)12 周。结果表明,TPP 暴露会导致肝功能和细胞器损伤,总胆固醇和甘油三酯水平升高。低剂量 TPP 暴露通过主要组织相容性复合体相关蛋白(参与抗原加工和呈递)破坏肝脏免疫系统。高剂量 TPP 暴露导致不饱和脂肪酸和类固醇激素生物合成紊乱,从而导致肝脏脂质积累。虽然 10μg/kg TPP 不会在肝脏中引起严重的脂质代谢紊乱,但观察到脂肪酸结合蛋白 5、苹果酸酶 1 等相关 SCPs 的显著过度表达,导致胆固醇代谢和脂肪生成紊乱,激活增殖剂激活受体信号通路,从而引发潜在的肥胖风险。此外,TPP 相关的脂质代谢紊乱在 HFF 饮食下加剧,通过改变细胞色素 P450 酶亚家族的活性,损害了小鼠的肝线粒体和内质网功能。这些发现深入了解了在不同饮食条件下亚慢性 TPP 暴露相关的分子毒性机制和健康风险。