Elevation of neuron-specific enolase and S-100β protein level in experimental acute spinal cord injury

被引:59
作者
Cao, Fei [1 ]
Yang, Xiao-feng [1 ]
Liu, Wei-guo [2 ]
Hu, Wei-wei [2 ]
Li, Gu [2 ]
Zheng, Xiu-jue [2 ]
Shen, Fang [2 ]
Zhao, Xue-qun [2 ]
Lv, Shi-ting [2 ]
机构
[1] Zhejiang Univ, Sch Med, Affiliated Hosp 1, Dept Neurosurg, Hangzhou 310009, Zhejiang, Peoples R China
[2] Zhejiang Univ, Sch Med, Affiliated Hosp 2, Dept Neurosurg, Hangzhou 310003, Zhejiang, Peoples R China
关键词
spinal cord injury; neuron-specific enolase; S-100 beta protein; biomarker;
D O I
10.1016/j.jocn.2007.05.014
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
We evaluated the protein levels of neuron-specific enolase (NSE) and S-100 beta in serum and cerebrospinal fluid (CSF) in an animal model of acute spinal cord injury and ascertained their relevance. Spinal cord injury was induced at the T8 level in rats. Enzyme-linked immunosorbent assay was used to measure the protein levels of NSE and S-100 beta in both serum and CSF at different time points (30 min, 2 h, 6 h, 12 h and 24 h after induction of spinal cord injury). There existed a significant correlation between neurological deficits and the severity of spinal cord injury (p < 0.05). Compared with the control group, the protein levels of NSE and S-100 beta in serum and CSF significantly increased from 2 h after injury (p < 0.05) and reached a maximum at 6 h. Within a certain time window, the protein levels of NSE and S-100 beta in serum and CSF were closely related to the severity of injury level (p < 0.05). The protein levels of NSE and S-100 beta in serum and CSF significantly increased after experimental spinal cord injury in a time-dependent manner and thus may be considered specific biomarkers for acute spinal cord injury. (C) 2007 Elsevier Ltd. All rights reserved.
引用
收藏
页码:541 / 544
页数:4
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