醒脑静注射液对戊四唑慢性癫痫点燃模型大鼠脑c-fos和c-jun蛋白表达的影响

Ji-Wei Cheng, Yu Bai, Xiao-jing Zhang, Lijun Zhang, Yuqing Hou
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引用次数: 1

摘要

目的:探讨醒脑静注射液对大鼠癫痫点燃模型(KME)抗癫痫作用的分子生物学机制。每组10只。干预药物在造模药物前30分钟给药,每天1次,连续5周。各组在使用干预药物30 min后腹腔注射造模药物戊四唑,每天1次,连续4周建立KME (BC组除外)。BC组给予生理盐水替代。所有药物均经腹腔注射。每天给药1 h后观察各组大鼠的行为。最后一次引燃试验在第5周末进行。实验结束时,采用免疫组化方法观察各组大鼠脑中c-fos和c-jun蛋白的表达情况。结果:M组大鼠脑内有大量c-fos和c-jun蛋白阳性细胞。结论:XNJ注射液对大鼠KME的抗癫痫作用可能与其阻断大鼠脑c-fos和c-jun蛋白的表达有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Influence of Xingnaojing Injection on the Expression of c-fos and c-jun Proteins in Brains of Rats in a Kindling Model of Epilepsy Chronically Induced by Pentetrazol
Objective: To investigate the molecular biological mechanism of the antiepileptic effect of Xingnaojing (XNJ) injection on a rat kindling model of epilepsy (KME). Methods: Fifty healthy 6-week-old male Sprague-Dawley rats were divided into the following five groups: blank control (BC) group, model (M) group, XNJ injection (XI) group, phenobarbital injection (PI) group and XNJ combined with phenobarbital (XP) group. There were 10 rats in each group. The intervention drugs were administered 30 min before the model-building drugs once a day for 5 weeks. The model-building drug pentetrazol was given to each group as an intraperitoneal injection 30 min after the use of the intervention drug once a day for 4 weeks for KME establishment (except for the BC group). The BC group was given physiological saline instead. All drugs were injected intraperitoneally. The behaviors of each group of rats were observed after the use of the model-building drugs for 1 h every day. The last kindling test was carried out at the end of week 5. Then, c-fos and c-jun protein expressions in the rat brains of each group were observed and analyzed by immunohistochemistry at the end of the experiment. Results: There was a large number of cells positive for the c-fos and c-jun proteins in the rat brains of the M group. Compared with the M group, the expression level of the c-fos and c-jun proteins was lower in the rat brains of the XI and PI groups (p < 0.01). There was no statistical difference between the XI and PI groups (p > 0.05). The number of positive cells in the rat brains of the XP group was even smaller than that of the XI or PI groups. Conclusion: The antiepileptic effect of the XNJ injection on the rat KME is probably related to its interruption function on the expression of the c-fos and c-jun proteins in rat brains.
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