Medical College of Soochow University, 215123, Suzhou, People's Republic of China.
Nanoscale Res Lett. 2009 Aug 1;4(11):1275-85. doi: 10.1007/s11671-009-9393-8.
Although it is known that nano-TiO2or other nanoparticles can induce liver toxicities, the mechanisms and the molecular pathogenesis are still unclear. In this study, nano-anatase TiO2(5 nm) was injected into the abdominal cavity of ICR mice for consecutive 14 days, and the inflammatory responses of liver of mice was investigated. The results showed the obvious titanium accumulation in liver DNA, histopathological changes and hepatocytes apoptosis of mice liver, and the liver function damaged by higher doses nano-anatase TiO2. The real-time quantitative RT-PCR and ELISA analyses showed that nano-anatase TiO2can significantly alter the mRNA and protein expressions of several inflammatory cytokines, including nucleic factor-κB, macrophage migration inhibitory factor, tumor necrosis factor-α, interleukin-6, interleukin-1β, cross-reaction protein, interleukin-4, and interleukin-10. Our results also implied that the inflammatory responses and liver injury may be involved in nano-anatase TiO2-induced liver toxicity.
虽然已知纳米 TiO2 或其他纳米颗粒会引起肝脏毒性,但作用机制和分子发病机制尚不清楚。在这项研究中,将纳米锐钛矿 TiO2(5nm)注入 ICR 小鼠腹腔内,连续 14 天,研究了纳米 TiO2 对小鼠肝脏的炎症反应。结果表明,小鼠肝脏中 DNA 明显的钛蓄积、组织病理学变化和肝细胞凋亡,以及较高剂量纳米锐钛矿 TiO2 对肝功能的损害。实时定量 RT-PCR 和 ELISA 分析表明,纳米锐钛矿 TiO2 可显著改变几种炎症细胞因子(包括核因子-κB、巨噬细胞移动抑制因子、肿瘤坏死因子-α、白细胞介素-6、白细胞介素-1β、交叉反应蛋白、白细胞介素-4 和白细胞介素-10)的 mRNA 和蛋白表达。我们的结果还表明,炎症反应和肝损伤可能与纳米锐钛矿 TiO2 诱导的肝毒性有关。