Molecular mechanism of hippocampal apoptosis of mice following exposure to titanium dioxide nanoparticles

被引:171
作者
Hu, Renping [3 ]
Zheng, Lei [3 ]
Zhang, Ting [1 ,2 ]
Gao, Guodong [3 ]
Cui, Yaling [3 ]
Cheng, Zhe [3 ]
Cheng, Jie [3 ]
Hong, Mengmeng [3 ]
Tang, Meng [1 ,2 ]
Hong, Fashui [3 ]
机构
[1] Southeast Univ, Minist Educ, Sch Publ Hlth, Key Lab Environm Med & Engn, Nanjing 210009, Peoples R China
[2] Southeast Univ, Jiangsu Key Lab Biomat & Devices, Nanjing 210009, Peoples R China
[3] Soochow Univ, Coll Med, Suzhou 215123, Peoples R China
基金
中国国家自然科学基金;
关键词
Titanium dioxide nanoparticles; Mice; Hippocampus; Apoptotic pathway; CENTRAL-NERVOUS-SYSTEM; OXIDATIVE STRESS; CELL-DEATH; MITOCHONDRIAL PATHWAY; TIO2; NANOPARTICLES; QUANTITATIVE PCR; BRAIN MICROGLIA; BEAS-2B CELLS; PARTICLES; NECROSIS;
D O I
10.1016/j.jhazmat.2011.04.027
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
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. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:32 / 40
页数:9
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