期刊
JOURNAL OF NEUROTRAUMA
卷 27, 期 11, 页码 2055-2066出版社
MARY ANN LIEBERT INC
DOI: 10.1089/neu.2010.1491
关键词
incomplete spinal cord injury; Nogo; Nogo receptor; plasticity; rehabilitation; task specificity
资金
- National Institute of Neurological Disorders and Stroke
- Falk Medical Research Trust
- Christopher and Dana Reeve Foundation
- Wings for Life Foundation
We tested the ability of two plasticity-promoting approaches to enhance recovery in a mouse model of incomplete spinal cord injury (SCI). Genetically, we reduced myelin-mediated inhibition of neural plasticity through Nogo66-receptor (NgR) gene deletion. Behaviorally, we utilized a novel multimodal exercise training paradigm. Adult mice of wild-type or NgR-null genotype were subjected to partial lateral hemisection (LHx) at C3-C4 with the intent of producing anatomically and functionally mild deficits. Exercise training or control treatment proceeded for 14 weeks. Behavioral outcomes were assessed prior to tract tracing and histological analysis. Genotype and training exerted differing effects on performance; training improved performance on a test related to the training regimen (task-specific benefit), whereas genotype also improved performance on more generalized behaviors (task-non-specific benefit). There were no significant histological differences across genotype or training assignment with regard to lesion size or axonal tract staining. Thus either NgR gene deletion or exercise training benefits mice with mild cervical spinal injury. In this lesion model, the effects of NgR deletion and training were not synergistic for the tasks assessed. Further work is required to optimize the interaction between pharmacological and physical interventions for SCI.
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