Brain Distribution and Toxicological Evaluation of a Systemically Delivered Engineered Nanoscale Ceria

被引:87
作者
Hardas, Sarita S. [2 ]
Butterfield, David Allan [2 ,3 ]
Sultana, Rukhsana [2 ]
Tseng, Michael T. [4 ]
Dan, Mo [1 ,5 ]
Florence, Rebecca L. [1 ]
Unrine, Jason M. [6 ]
Graham, Uschi M. [7 ]
Wu, Peng [8 ]
Grulke, Eric A. [8 ]
Yokel, Robert A. [1 ,5 ]
机构
[1] Univ Kentucky, Dept Pharmaceut Sci, Acad Med Ctr, Lexington, KY 40536 USA
[2] Univ Kentucky, Dept Chem, Lexington, KY 40506 USA
[3] Univ Kentucky, Ctr Membrane Sci, Lexington, KY 40506 USA
[4] Univ Louisville, Dept Anat Sci & Neurobiol, Louisville, KY 40202 USA
[5] Univ Kentucky, Grad Ctr Toxicol, Acad Med Ctr, Lexington, KY 40506 USA
[6] Univ Kentucky, Dept Plant & Soil Sci, Lexington, KY 40546 USA
[7] Univ Kentucky, Ctr Appl Energy Res, Lexington, KY 40511 USA
[8] Univ Kentucky, Dept Chem & Mat Engn, Lexington, KY 40506 USA
关键词
blood-brain barrier; ceria; hippocampus; neurotoxicity; oxidative injury; rat; OXIDATIVE STRESS; OXIDE NANOPARTICLES; GOLD NANOPARTICLES; FREE-RADICALS; TRANSLOCATION; PARTICLES; BIODISTRIBUTION; NEUROTOXICITY; CYTOTOXICITY; GLUTATHIONE;
D O I
10.1093/toxsci/kfq137
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
Engineered nanoscale ceria is used as a diesel fuel catalyst. Little is known about its mammalian central nervous system effects. The objective of this paper is to characterize the biodistribution of a 5-nm citrate-stabilized ceria dispersion from blood into brain and its pro- or antioxidant effects. An similar to 4% aqueous ceria dispersion was iv infused into rats (0, 100, and up to 250 mg/kg), which were terminated after 1 or 20 h. Ceria concentration, localization, and chemical speciation in the brain were assessed by inductively coupled plasma mass spectrometry, light and electron microscopy (EM), and electron energy loss spectroscopy (EELS). Pro- or antioxidative stress effects were assessed as protein carbonyls, 3-nitrotyrosine, and protein-bound 4-hydroxy-2-trans-nonenal in hippocampus, cortex, and cerebellum. Glutathione reductase, glutathione peroxidase, manganese superoxide dismutase, and catalase levels and activities were measured in hippocampus. Catalase levels and activities were also measured in cortex and cerebellum. Na fluorescein and horseradish peroxidase (HRP) were given iv as blood-brain barrier (BBB) integrity markers. Mortality was seen after administration of 175-250 mg ceria/kg. Twenty hours after infusion of 100 mg ceria/kg, brain HRP was marginally elevated. EM and EELS revealed mixed Ce(III) and Ce(IV) valence in the freshly synthesized ceria in vitro and in ceria agglomerates in the brain vascular compartment. Ceria was not seen in microvascular endothelial or brain cells. Ceria elevated catalase levels at 1 h and increased catalase activity at 20 h in hippocampus and decreased catalase activity at 1 h in cerebellum. Compared with a previously studied similar to 30-nm ceria, this ceria was more toxic, was not seen in the brain, and produced little oxidative stress effect to the hippocampus and cerebellum. The results are contrary to the hypothesis that a smaller engineered nanomaterial would more readily permeate the BBB.
引用
收藏
页码:562 / 576
页数:15
相关论文
共 41 条
[1]   Differential expression of peroxisomal matrix and membrane proteins during postnatal development of mouse brain [J].
Ahlemeyer, Barbara ;
Neubert, Inge ;
Kovacs, Werner J. ;
Baumgart-Vogt, Eveline .
JOURNAL OF COMPARATIVE NEUROLOGY, 2007, 505 (01) :1-17
[2]   Neurodegenerative disorders in humans: the role of glutathione in oxidative stress-mediated neuronal death [J].
Bains, JS ;
Shaw, CA .
BRAIN RESEARCH REVIEWS, 1997, 25 (03) :335-358
[3]  
Balbus JM, 2007, ENVIRON HEALTH PERSP, V115, P1654, DOI [10.1289/ehp.10327, 10.1289/chp.10327]
[4]  
Bhabra G, 2009, NAT NANOTECHNOL, V4, P876, DOI [10.1038/NNANO.2009.313, 10.1038/nnano.2009.313]
[5]   In vitro cytotoxicity of oxide nanoparticles: Comparison to asbestos, silica, and the effect of particle solubility [J].
Brunner, Tobias J. ;
Wick, Peter ;
Manser, Pius ;
Spohn, Philipp ;
Grass, Robert N. ;
Limbach, Ludwig K. ;
Bruinink, Arie ;
Stark, Wendelin J. .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2006, 40 (14) :4374-4381
[6]  
Butterfield D.A., 1997, ADV CELL AGING GERON, V2, P161
[7]   beta-Amyloid-associated free radical oxidative stress and neurotoxicity: Implications for Alzheimer's disease [J].
Butterfield, DA .
CHEMICAL RESEARCH IN TOXICOLOGY, 1997, 10 (05) :495-506
[8]   Proteomic identification of oxidatively modified proteins in Alzheimer's disease brain. Part 1: Creatine kinase bb, glutamine synthase, and ubiquitin carboxy-terminal hydrolase L-1 [J].
Castegna, A ;
Aksenov, M ;
Aksenova, M ;
Thongboonkerd, V ;
Klein, JB ;
Pierce, WM ;
Booze, R ;
Markesbery, WR ;
Butterfield, DA .
FREE RADICAL BIOLOGY AND MEDICINE, 2002, 33 (04) :562-571
[9]   Rare earth nanoparticles prevent retinal degeneration induced by intracellular peroxides [J].
Chen, Junping ;
Patil, Swanand ;
Seal, Sudipta ;
McGinnis, James F. .
NATURE NANOTECHNOLOGY, 2006, 1 (02) :142-150
[10]   Determining the size and shape dependence of gold nanoparticle uptake into mammalian cells [J].
Chithrani, BD ;
Ghazani, AA ;
Chan, WCW .
NANO LETTERS, 2006, 6 (04) :662-668