Akt1在颞叶癫痫大鼠海马中的表达变化  

The expression of Aktl in hippocampus of rat model of temporal lobe epilepsy at different time

作　　者：林慧慧[1] 刘艳青[2] 刘淼[1] 李江丽[1] 宋毅军[3] 

机构地区：[1]天津医科大学七年制2006级,300070 [2]天津医科大学研究生院2007级,300070 [3]天津医科大学总医院神经内科,300052

出　　处：《中国现代神经疾病杂志》2012年第5期581-588,共8页Chinese Journal of Contemporary Neurology and Neurosurgery

基　　金：国家自然科学基金资助项目(项目编号:91132722),国家自然科学基金资助项目(项目编号:81071044);天津市自然科学基金资助项目(项目编号:10JCYBJC13800);天津市高等学校科技发展基金资助项目(项目编号:20090123);天津医科大学新世纪人才支持计划项目~~

摘　　要：目的研究颞叶癫癎模型海马区神经元Akt1表达变化,探讨其在癫癎发生发展中的作用。方法采用氯化锂-匹罗卡品方法制备颞叶癫癎大鼠模型,Western blotting检测海马区总蛋白、Quantity one软件行灰度值分析;免疫组织化学染色观察海马各区Akt1蛋白表达变化,计数不同处理组阳性神经元数目。结果 Western blotting检测结果显示,与正常对照组相比,癫癎模型组大鼠于癫癎持续状态发作即刻海马区Akt1蛋白表达升高(t=2.445,P=0.034),并于第30天时达峰值水平(t=1.214,P=0.002),发作后24 h表达水平迅速降低,并低于正常值范围(t=4.294,P=0.000),其余各测量时间点表达无明显改变;与氯化锂组相比,癫癎模型组大鼠于癫癎持续状态后1h海马区Akt1蛋白表达开始降低,24 h降至最低水平(t=4.134,P=0.000),至发作48 h后开始逐渐升高(t=2.481,P=0.002),并于发作第7天时升至氯化锂组水平。免疫组织化学染色显示,癫癎持续状态发作后海马CA3区Akt1蛋白表达阳性神经元数目立即增加,12h达高峰(t=16.586,P=0.000),48 h减少并降至正常值水平(t=0.357,P=0.089),发作后第10天再次增加(t=3.123,P=0.000),于第30天时阳性神经元数目再次达峰值水平(t=18.339,P=0.000),第50天开始恢复至正常值水平(t=3.219,P=0.000);氯化锂组仅海马CA3区Akt1蛋白表达于实验初始(0 h)升高并高于正常对照组(P<0.05),海马CA1和CA2区Akt1蛋白表达变化组间差异均无统计学意义(P>0.05)。结论海马及海马CA3区Akt1蛋白表达均呈现癫癎持续状态后升高、降低、再升高的动态过程,提示可能存在神经元保护作用,对抗细胞凋亡、促进细胞存活。Objective To study the expression of Aktl in hippocampal neurons in temporal lobe epilepsy, and explore its role in the development of epilepsy. Methods Two hundred and ten healthy adult male Sprague-Dawley （SD） rats were randomly divided into normal group （n = 10）, lithium chloride （LiC1） group （n = 10） and epilepsy group （n = 190）. LiCl-pilocarpine （PILO） was used for animal model of epilepsy. Total protein was extracted from hippocampus and rat brain slices were obtained at different time points （0 h, 1 h, 6 h, 12 h, 24 h, 48 h, 7 d, 10 d, 30 d, 50 d） after status epilepticus （SE） in normal group and LiC1 group. Western blotting technique was used for detection of total protein in the hippocampus, and gray value was analyzed by Quantity one software. Immunohistochemical staining was used to detect the expression of Aktl protein in the hippocampus and microscopic counting method （~ 200） was used to quantify positive nerve cells in hippocampal region. Results Compared with the control group, the expression of Aktl protein in the hippocampus in epilepsy group was significantly increased at the beginning of SE and achieved to the peak at 30 d after SE （0 h： 4.09 ± 0.04, t = 2.445, P = 0.034; 30 d： 0.52 ± 0.03, t = 1.214, P = 0.002）. The expression level was quickly reduced and was lower than normal value at 24 h after SE （0.27 ±- 0.06, t = 4.294, P = 0.000）, and no significant differences were seen at other time points. In comparison with LiC1 group, the Aktl protein expression in hippocampus in epilepsy group began to decrease at 1 h after SE, and reached to the lowest level at 24 h after SE （0.27-± 0.06, t = 4.134, P -- 0.000）. At 48 h after SE the Aktl expression began to increase and achieved to the ｜evel of LiC1 group at 7 d after SE. In immunohistochemical staining： Aktl protein positive cells in hippocampal CA3 area immediately increased after SE and achieved to the peak （46.70 -± 2.90） at 12 h after SE, but decreased to normal level （16.20

关 键 词：蛋白激酶类 海马 癫癎 免疫印迹法 免疫组织化学 疾病模型 动物 

分 类 号：R742.1[医药卫生—神经病学与精神病学]