Zhang Weidong, Zhao Yong, Li Fuli, Li Lan, Feng Yanni, Min Lingjiang, Ma Dongxue, Yu Shuai, Liu Jing, Zhang Hongfu, Shi Tianhong, Li Fuwei, Shen Wei
College of Life Sciences, Qingdao Agricultural University, Qingdao, China.
State Key Laboratory of Animal Nutrition, Institute of Animal Sciences, Chinese Academy of Agricultural Sciences, Beijing, China.
Front Pharmacol. 2018 Jan 30;9:57. doi: 10.3389/fphar.2018.00057. eCollection 2018.
Zinc oxide nanoparticles (ZnO NPs), known for their chemical stability and strong adsorption, are used in everyday items such as cosmetics, sunscreens, and prophylactic drugs. However, they have also been found to adversely affect organisms; previously we found that ZnO NPs disrupt pubertal ovarian development, inhibit embryonic development by upsetting γ-H2AX and NF-κB pathways, and even disturb skin stem cells. Non-targeted metabolomic analysis of biological organisms has been suggested as an unbiased tool for the investigation of perturbations in response to NPs and their underlying mechanisms. Although metabolomics has been used in nanotoxicological studies, very few reports have used it to investigate the effects of ZnO NPs exposure. In the current investigation, through a metabolomics-based approach, we discovered that ZnO NPs caused changes in plasma metabolites involved in anti-oxidative mechanisms, energy metabolism, and lipid metabolism in hen livers. These results are in line with earlier findings that ZnO NPs perturb the tricarboxylic acid cycle and in turn result in the use of alternative energy sources. We also found that ZnO NPs disturbed lipid metabolism in the liver and consequently impacted blood lipid balance. Changes in plasma metabolomes were correlated with hepatic steatosis.
氧化锌纳米颗粒(ZnO NPs)以其化学稳定性和强吸附性而闻名,被用于化妆品、防晒霜和预防药物等日常用品中。然而,人们也发现它们会对生物体产生不利影响;此前我们发现,ZnO NPs会扰乱青春期卵巢发育,通过干扰γ-H2AX和NF-κB途径抑制胚胎发育,甚至扰乱皮肤干细胞。非靶向代谢组学分析被认为是一种用于研究生物体对纳米颗粒的反应及其潜在机制的无偏工具。尽管代谢组学已被用于纳米毒理学研究,但很少有报告用它来研究ZnO NPs暴露的影响。在当前的研究中,通过基于代谢组学的方法,我们发现ZnO NPs导致母鸡肝脏中参与抗氧化机制、能量代谢和脂质代谢的血浆代谢物发生变化。这些结果与早期的发现一致,即ZnO NPs扰乱三羧酸循环,进而导致使用替代能源。我们还发现,ZnO NPs扰乱了肝脏中的脂质代谢,从而影响了血脂平衡。血浆代谢组的变化与肝脂肪变性相关。