Song Bin, Zhou Ting, Yang WenLong, Liu Jia, Shao LongQuan
Guizhou Provincial People's Hospital, Guiyang 550002, China; Nanfang Hospital, Southern Medical University, Guangzhou 510515, China.
Guizhou Provincial People's Hospital, Guiyang 550002, China.
Environ Toxicol Pharmacol. 2016 Dec;48:130-140. doi: 10.1016/j.etap.2016.10.013. Epub 2016 Oct 18.
With the rapid development of nanotechnology, titanium dioxide nanoparticles (TNPs) are widely used in many fields. People in such workplaces or researchers in laboratories are at a higher risk of being exposed to TNPs, so are the consumers. Moreover, increasing evidence revealed that the concentrations of TNPs are elevated in animal organs after systematic exposure and such accumulated TNPs could induce organ dysfunction. Although cellular responses such as oxidative stress, inflammatory response, apoptosis, autophagy, signaling pathways, and genotoxic effects contribute to the toxicity of TNPs, the interrelationship among them remains obscure. Given the pivotal role of oxidative stress, we summarized relevant articles covering the involvement of oxidative stress in TNPs' toxicity and found that TNP-induced oxidative stress might play a central role in toxic mechanisms. However, available data are far from being conclusive and more investigations should be performed to further confirm whether the toxicity of TNPs might be attributed in part to the cascades of oxidative stress. Tackling this uncertain issue may help us to comprehensively understand the interrelationship among toxic cellular responses induced by TNPs and might shed some light on methods to alleviate toxicity of TNPs.
随着纳米技术的迅速发展,二氧化钛纳米颗粒(TNPs)在许多领域得到广泛应用。在这些工作场所的人员或实验室研究人员接触TNPs的风险较高,消费者也是如此。此外,越来越多的证据表明,经系统暴露后动物器官中TNPs的浓度会升高,而这些累积的TNPs会诱发器官功能障碍。尽管诸如氧化应激、炎症反应、细胞凋亡、自噬、信号通路和遗传毒性效应等细胞反应会导致TNPs的毒性,但其之间的相互关系仍不清楚。鉴于氧化应激的关键作用,我们总结了有关氧化应激参与TNPs毒性作用的相关文章,发现TNP诱导的氧化应激可能在毒性机制中起核心作用。然而,现有数据远非结论性的,需要进行更多研究以进一步证实TNPs的毒性是否部分归因于氧化应激的级联反应。解决这个不确定的问题可能有助于我们全面理解TNPs诱导的毒性细胞反应之间的相互关系,并可能为减轻TNPs毒性的方法提供一些启示。