Environmental Enrichment Mitigates Deficits after Repetitive Mild Traumatic Brain Injury

被引:29
作者
Liu, Xixia [1 ]
Qiu, Jianhua [2 ,3 ]
Alcon, Sasha [2 ]
Hashim, Jumana [2 ]
Meehan, William P., III [2 ,3 ,4 ,5 ]
Mannix, Rebekah [2 ,3 ]
机构
[1] Peoples Hosp Guangxi Zhuang Autonomous Reg, Nanning, Peoples R China
[2] Boston Childrens Hosp, Div Emergency Med, 300 Longwood Ave, Boston, MA 02115 USA
[3] Harvard Med Sch, Boston, MA USA
[4] Sports Concuss Clin, Div Sports Med, Boston, MA USA
[5] Micheli Ctr Sports Injury Prevent, Waltham, MA USA
关键词
animal model; concussion; enrichment; mild traumatic brain injury; synaptic plasticity; ALZHEIMERS-DISEASE; SYNAPTIC PLASTICITY; RATS; RECOVERY; EXPRESSION; SUBUNIT; MICE; PHOSPHORYLATION; INCREASES; NEURODEGENERATION;
D O I
10.1089/neu.2016.4823
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Although environmental enrichment has been shown to improve functional and histologic outcomes in pre-clinical moderate-to-severe traumatic brain injury (TBI), there are a paucity of pre-clinical data regarding enrichment strategies in the setting of repetitive mild traumatic brain injury (rmTBI). Given the vast numbers of athletes and those in the military who sustain rmTBI, the mounting evidence of the long-term and progressive sequelae of rmTBI, and the lack of targeted therapies to mitigate these sequelae, successful enrichment interventions in rmTBI could have large public health significance. Here, we evaluated enrichment strategies in an established pre-clinical rmTBI model. Seventy-one male C57BL/6 mice were randomized to two different housing conditions, environmental enrichment (EE) or normal condition (NC), then subjected to rmTBI injury (seven injuries in 9 days) or sham injury (anesthesia only). Functional outcomes in all four groups (NC-TBI, EE-TBI, NC-sham, and EE-sham) were assessed by motor, exploratory/anxiety, and mnemonic behavioral tests. At the synaptic level, N-methyl D-aspartate receptor (NMDAR) subunit expression of phosphorylated glutamate receptor 1 (GluR1), phosphorylated Ca2+/calmodulin-dependent protein kinase II (CaMKII), and calpain were evaluated by western blot. Compared to injured NC-TBI mice, EE-TBI mice had improved memory and decreased anxiety and exploratory activity post-injury. Treatment with enrichment also corresponded to normal NMDAR subunit expression, decreased GluR1 phosphorylation, decreased phosphorylated CaMKII, and normal calpain expression post-rmTBI. These data suggest that enrichment strategies may improve functional outcomes and mitigate synaptic changes post-rmTBI. Given that enrichment strategies are feasible in the clinical setting, particularly for athletes and soldiers for whom the risk of repetitive injury is greatest, these data suggest that clinical trials may be warranted.
引用
收藏
页码:2445 / 2455
页数:11
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