Autor: |
Zhao Song, Yu Zhanyang, Zhao Gang, Xing Changhong, Hayakawa Kazuhide, Whalen Michael J, Lok Josephine M, Lo Eng H, Wang Xiaoying |
Jazyk: |
angličtina |
Rok vydání: |
2012 |
Předmět: |
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Zdroj: |
BMC Neuroscience, Vol 13, Iss 1, p 67 (2012) |
Druh dokumentu: |
article |
ISSN: |
1471-2202 |
DOI: |
10.1186/1471-2202-13-67 |
Popis: |
Abstract Background Accumulating evidence has demonstrated that over-expression of Neuroglobin (Ngb) is neuroprotective against hypoxic/ischemic brain injuries. In this study we tested the neuroprotective effects of Ngb over-expression against traumatic brain injury (TBI) in mice. Results Both Ngb over-expression transgenic (Ngb-Tg) and wild-type (WT) control mice were subjected to TBI induced by a controlled cortical impact (CCI) device. TBI significantly increased Ngb expression in the brains of both WT and Ngb-Tg mice, but Ngb-Tg mice had significantly higher Ngb protein levels at the pre-injury baseline and post-TBI. Production of oxidative tissue damage biomarker 3NT in the brain was significantly reduced in Ngb-Tg mice compared to WT controls at 6 hours after TBI. The traumatic brain lesion volume was significantly reduced in Ngb Tg mice compared to WT mice at 3 weeks after TBI; however, there were no significant differences in the recovery of sensorimotor and spatial memory functional deficits between Ngb-Tg and WT control mice for up to 3 weeks after TBI. Conclusion Ngb over-expression reduced traumatic lesion volume, which might partially be achieved by decreasing oxidative stress. |
Databáze: |
Directory of Open Access Journals |
Externí odkaz: |
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