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单核细胞趋化蛋白-1在难治性癫痫患者脑组织中的表达

Expression of monocyte chemoattractant protein-1 in brain tissue of patients with intractable epilepsy.

作者信息

Wu Y, Wang X, Mo X, Xi Z, Xiao F, Li J, Zhu X, Luan G, Wang Y, Li Y, Zhang J

机构信息

Department of Neurology, The First Affiliated Hospital, Chongqing Medical University, Chongqing, China.

出版信息

Clin Neuropathol. 2008 Mar-Apr;27(2):55-63. doi: 10.5414/npp27055.

Abstract

OBJECTIVE

To investigate the expression ofmonocyte chemoattractant protein-1 (MCP-1) in the brain tissue of patients with intractable epilepsy (IE) and to explore its role in the pathogenesis of IE.

MATERIAL

Patients with IE were collected from the Department of Neurosurgery of several Chinese hospitals between 2002 and 2005. The average age of these 40 patients was 23.65 +/- 10.14 (X +/- SD) years (11 - 58 years), with 19 males and 21 females. In addition to the typical symptoms and distinct EEG features of epilepsy, all recruited patients met the requirements of intractable epilepsy.

METHODS

On the basis of positive results obtained from gene chip analysis, the expression of MCP-1 was first investigated in the brain tissue of IE patients (40 cases) using Western Blotting and immunohistochemistry and then compared with the controls.

RESULTS

Gene chip scanning demonstrated that expression of MCP-1 mRNA was upregulated in the brain tissue of patients with IE. Western Blotting and immunohistochemical experiments further confirmed that, as compared with that in the control group, expression of MCP-1 protein was significantly increased in the IE patients (p < 0.05).

CONCLUSION

These results suggest that MCP-1 are involved in the pathogenesis of IE.

摘要

目的

探讨单核细胞趋化蛋白-1(MCP-1)在难治性癫痫(IE)患者脑组织中的表达情况,并探讨其在IE发病机制中的作用。

材料

2002年至2005年间从几家中国医院神经外科收集IE患者。这40例患者的平均年龄为23.65±10.14(X±SD)岁(11 - 58岁),其中男性19例,女性21例。除了具有癫痫的典型症状和明显的脑电图特征外,所有入选患者均符合难治性癫痫的标准。

方法

在基因芯片分析获得阳性结果的基础上,首先采用蛋白质印迹法和免疫组织化学方法研究40例IE患者脑组织中MCP-1的表达情况,然后与对照组进行比较。

结果

基因芯片扫描显示,IE患者脑组织中MCP-1 mRNA表达上调。蛋白质印迹法和免疫组织化学实验进一步证实,与对照组相比,IE患者MCP-1蛋白表达显著增加(p < 0.05)。

结论

这些结果表明MCP-1参与了IE的发病机制。

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