Medical College, Soochow University, Suzhou, China.
J Hazard Mater. 2011 Jul 15;191(1-3):32-40. doi: 10.1016/j.jhazmat.2011.04.027. Epub 2011 Apr 22.
Previous studies demonstrate that the exposure to titanium dioxide nanoparticles (TiO(2) NPs) damages the central nervous system of mice; however, very little is known about the effects of TiO(2) NPs on hippocampal apoptosis or its molecular mechanism. The present study investigated the molecular mechanism associated with hippocampal apoptosis in mice induced by intragastric administration of TiO(2) NPs for consecutive 60 days. Our findings indicate that TiO(2) NPs accumulate in the mouse hippocampus, and this accumulation, in turn, led to hippocampal apoptosis and impairment in spatial recognition memory in mice. In addition, TiO(2) NPs significantly activated caspase-3 and -9, inhibited Bcl-2, and promoted the levels of Bax and cytochrome c. Furthermore, TiO(2) NPs induced accumulation of reactive oxygen species in the mouse hippocampus. These findings suggest that TiO(2) NP-induced apoptosis in the mouse hippocampus may result from an intrinsic pathway, and workers and consumers should take great caution when handling nanomaterials.
先前的研究表明,二氧化钛纳米粒子(TiO(2) NPs)暴露会损害小鼠的中枢神经系统;然而,关于 TiO(2) NPs 对海马细胞凋亡的影响及其分子机制知之甚少。本研究探讨了连续 60 天经胃内给予 TiO(2) NPs 诱导小鼠海马细胞凋亡相关的分子机制。我们的研究结果表明,TiO(2) NPs 在小鼠海马中蓄积,这种蓄积反过来导致了小鼠海马细胞凋亡和空间识别记忆损伤。此外,TiO(2) NPs 显著激活了 caspase-3 和 -9,抑制了 Bcl-2,并促进了 Bax 和细胞色素 c 的水平。此外,TiO(2) NPs 诱导了小鼠海马中活性氧的积累。这些发现表明,TiO(2) NPs 诱导的小鼠海马细胞凋亡可能是由内在途径引起的,因此在处理纳米材料时,工人和消费者应格外小心。