免疫球蛋白对惊厥大鼠及神经细胞c-fos表达的影响

Jing-wei Hu, Zhong-cheng Zhou
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引用次数: 1

摘要

目的探讨免疫球蛋白对惊厥大鼠的临床疗效及对神经细胞c-fos表达的影响。方法采用戊四氮唑(PTZ)诱导Wistar大鼠全身癫痫发作,建立癫痫模型。15只大鼠随机分为3组,即A组:正常对照组;B组:PTZ加静脉注射免疫球蛋白(IVIG);C组:PTZ加生理盐水(NS)。观察B组和c组大鼠癫痫发作情况,并比较B组和c组大鼠癫痫模型第14天各组大鼠灌注脑组织切片,采用免疫组化染色(ABC法)检测c-fos表达。结果(1)A组偶见脑组织c-fos表达较弱。(2)与C组大鼠比较,B组大鼠癫痫潜伏期明显延长,惊厥评分明显降低。b组无大鼠死亡,C组6只大鼠中有3只死于癫痫发作。癫痫发作的潜伏期有变短的趋势。C组大鼠惊厥评分无明显变化。(3)与C组相比,B组大鼠脑组织同一区域C -fos表达明显降低(P < 0.01)。结论IVIG可能具有抑制惊厥和降低c-fos表达的作用。关键词:免疫球蛋白;癫痫、部分;神经元;基因,安全系数;老鼠
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effects of immunoglobulin on convulsion rats and on c-fos expressions in neurocytes
Objective To explore clinical effects of immunoglobulin on convulsion rats and influences of immunoglobulin on the c-fos expression of neurocytes. Methods The epilepsy model was established by injecting pentylenetetrazol (PTZ) into Wistar rats to induce the generalized seizures. Fifteen rats were randomly divided into three groups, that is, group A: normal control; group B: PTZ plus intravenous immunoglobulin (IVIG) ; group C: PTZ plus normal saline (NS) . Seizure conditions of rats were observed and compared between group B and C. All perfused brain tissues of rats were sectioned and detected the c-fos expressions by immunohistochemistry staining (ABC method) at the 14th day of the epilepsy model. Results (1) In group A, weak c-fos expressions in brain tissues were observed occasionally. (2) Compared with rats of group C, the epilepsy in rats of group B showed obvious longer latencies and remarkably lower convulsion scores. No rat was dead in group B. While in group C 3of 6 rats died from seizures. Latencies of seizures showed a tendency to become short. There was no obvious change of convulsion scores in group C. (3) The c-fos expression in group B significantly decreased at the same region of brain tissues when compared with that in group C (P < 0.01) . Conclusion IVIG might play a role in the inhibition of convulsions and the reduction of the c-fos expressions. Key words: Immunoglobulins; Epilepsy, partial; Neurons; Genes, FOS; Rat
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