Cerium Oxide Nanoparticles Improve Outcome after In Vitro and In Vivo Mild Traumatic Brain Injury

被引:62
作者
Bailey, Zachary S. [1 ]
Nilson, Eric [2 ]
Bates, John A. [2 ]
Oyalowo, Adewole [1 ]
Hockey, Kevin S. [2 ]
Sajja, Venkata Siva Sai Sujith [1 ]
Thorpe, Chevon [2 ]
Rogers, Heidi [2 ]
Dunn, Bryce [1 ]
Frey, Aaron S. [2 ]
Billings, Marc J. [2 ]
Sholar, Christopher A. [2 ]
Hermundstad, Amy [1 ]
Kumar, Challa [3 ]
VandeVord, Pamela J. [1 ]
Rzigalinski, Beverly A. [2 ]
机构
[1] Virginia Tech, Dept Biomed Engn & Mech, Blacksburg, VA USA
[2] Edward Via Coll Osteopath Med, Dept Pharmacol, Res 2 Bldg,1861 Pratt Dr, Blacksburg, VA 24060 USA
[3] Harvard Univ, Rowland Inst Sci, Integrated Mesoscale Architectures Sustainable Ca, Cambridge, MA 02138 USA
关键词
cerium oxide; nanoparticles; oxidative stress; traumatic brain injury; OXIDATIVE STRESS; SUPEROXIDE-PRODUCTION; NITRIC-OXIDE; MODEL; NEUROPROTECTION; IMPAIRMENT; RADICALS; DEFICITS; MEMORY; CELLS;
D O I
10.1089/neu.2016.4644
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Mild traumatic brain injury results in aberrant free radical generation, which is associated with oxidative stress, secondary injury signaling cascades, mitochondrial dysfunction, and poor functional outcome. Pharmacological targeting of free radicals with antioxidants has been examined as an approach to treatment, but has met with limited success in clinical trials. Conventional antioxidants that are currently available scavenge a single free radical before they are destroyed in the process. Here, we report for the first time that a novel regenerative cerium oxide nanoparticle antioxidant reduces neuronal death and calcium dysregulation after in vitro trauma. Further, using an in vivo model of mild lateral fluid percussion brain injury in the rat, we report that cerium oxide nanoparticles also preserve endogenous antioxidant systems, decrease macromolecular free radical damage, and improve cognitive function. Taken together, our results demonstrate that cerium oxide nanoparticles are a novel nanopharmaceutical with potential for mitigating neuropathological effects of mild traumatic brain injury and modifying the course of recovery.
引用
收藏
页码:1452 / 1462
页数:11
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