School of Environmental Science and Engineering, Shanghai Jiao Tong University, Shanghai 200240, China.
School of Environmental Science and Engineering, Sun Yat-sen University, Guangzhou 510275, China.
Environ Sci Technol. 2020 Mar 17;54(6):3487-3498. doi: 10.1021/acs.est.0c00663. Epub 2020 Mar 2.
Much effort has been devoted to clarifying the comparative toxicity of ZnO nanoparticles (NPs) and Zn ions; however, little is known about their toxicodynamic processes at the metabolic level. Here, we investigated the acute (2d) and chronic (7d) effects to a soil species, , of two sublethal doses of ZnO-NPs and ZnCl (10 and 30 mg/L Zn) using ultrahigh performance liquid chromatography-quadrupole-time-of-flight/mass spectrometry-based metabolomics. The metabolomics analysis identified 99, 128, 121, and 183 significantly changed metabolites (SCMs) in exposed to ZnO-NPs for 2d, ZnCl for 2d, ZnO-NPs for 7d, and ZnCl for 7d, respectively, suggesting that ZnCl induced stronger metabolic reprogramming than ZnO-NPs, and a longer exposure time caused greater metabolite changes. Among the SCMs, 67 were shared by ZnO-NPs and ZnCl after 2d and 84 after 7d. These metabolites were mainly related to oxidative stress and antioxidant defense, membrane disturbance, and energy expenditure. The targeted analysis on physiological and biochemical responses further proved the metabolic observations. Nevertheless, 32 (33%) and 37 (31%) SCMs were found only in ZnO-NP treatments after 2 and 7d, respectively, suggesting that the toxicity of ZnO-NPs cannot be solely attributed to the released Zn ions. Metabolic pathway analysis revealed significant perturbations of galactose metabolism, amino sugar and nucleotide sugar metabolism, and glycerophospholipid metabolism in all test groups. Based on involvement frequency, glucose-1-phosphate, glycerol 3-phosphate, and phosphorylcholine could serve as universal biomarkers for exposure to different Zn forms. Four pathways perturbed by ZnO-NPs were nanospecific upon acute exposure and three upon chronic exposure. Our findings demonstrated that metabolomics is an effective tool for understanding the molecular toxicity mechanism and highlighted that time-series measurements are essential for discovering and comparing modes of action of metal ions and NPs.
人们投入了大量精力来阐明氧化锌纳米粒子(NPs)和 Zn 离子的相对毒性;然而,对于它们在代谢水平上的毒动学过程,人们知之甚少。在这里,我们使用基于超高效液相色谱-四极杆飞行时间/质谱联用的代谢组学方法,研究了两种亚致死剂量的 ZnO-NPs 和 ZnCl(10 和 30mg/L Zn)对一种土壤物种()的急性(2d)和慢性(7d)影响。代谢组学分析鉴定出了暴露于 ZnO-NPs 2d、ZnCl 2d、ZnO-NPs 7d 和 ZnCl 7d 的土壤中分别有 99、128、121 和 183 个显著变化的代谢物(SCMs),这表明 ZnCl 引起的代谢重编程比 ZnO-NPs 更强,并且暴露时间更长会导致更大的代谢物变化。在这些 SCMs 中,有 67 个在 ZnO-NPs 和 ZnCl 暴露 2d 后和 84 个在 7d 后被共享。这些代谢物主要与氧化应激和抗氧化防御、膜扰动和能量消耗有关。对生理生化反应的靶向分析进一步证明了代谢观察结果。然而,在 2d 和 7d 后分别只有 32(33%)和 37(31%)个 SCMs 仅在 ZnO-NP 处理中被发现,这表明 ZnO-NPs 的毒性不能仅仅归因于释放的 Zn 离子。代谢途径分析表明,所有实验组的半乳糖代谢、氨基糖和核苷酸糖代谢以及甘油磷脂代谢都受到了显著干扰。基于参与频率,葡萄糖-1-磷酸、甘油 3-磷酸和磷酸胆碱可以作为暴露于不同 Zn 形态的通用生物标志物。在急性暴露时,有 4 条途径因 ZnO-NPs 而发生纳米特异性改变,3 条途径在慢性暴露时发生改变。我们的研究结果表明,代谢组学是一种理解分子毒性机制的有效工具,并强调了时间序列测量对于发现和比较金属离子和 NPs 的作用模式至关重要。