Chen Ziyi, Chen Shuda, Chen Liujing, Zhou Jueqian, Dai Qilin, Yang Libai, Li Xiubin, Zhou Liemin
Department of Neurology, The First Affiliated Hospital, Sun Yat-sen University, 58th Zhongshan 2nd Road, Guangzhou, PR China.
Brain Res. 2009 May 13;1270:112-20. doi: 10.1016/j.brainres.2009.03.012. Epub 2009 Mar 21.
Voltage-gated sodium channels (VGSC) are important determinants of neuronal excitability which are implicated in the pathogenesis of epilepsy. Ankyrin-G contributes to the distribution and regulation of VGSC. Here we investigated the alterations of the two alpha-subunits SCN8A and SCN1A and their adapter ankyrin-G in the hippocampal cornu ammonis 1 (CA1) of rats after pilocarpine induced status epilepticus (PISE), compared to the sham-control group (C1) and blank-control group (C2). Significant increase of SCN8A mRNA (41.08% increase compared to C1, P<0.001; 30.88% increase compared to C2, P=0.011) was detected 60 days after PISE. At D1 SCN8A mRNA reduced but no significant changes were detected when compared to controls (one-way ANOVA, F=1.232, P=0.276). After measuring the optical density of Western blot, we detected significant differences between the levels of SCN8A protein in different groups but no difference between the protein levels of SCN1A at D1 and D60 after pilocarpine treatment compared to the control. At D60 the relative copies of ankyrin-G mRNA on internal control beta-actin in PISE group increased significantly compared to C1 and C2 (one-way ANOVA, F=16.537, P<0.001). Significantly increase of ankyrin-G immunoreactivity in Western blot from the PISE group 1 day and 60 days after PISE was observed, compared to the controls (one-way ANOVA, F=24.255 at D1, P<0.001; F=29.280 at D60, P<0.001). After analyzing the double-stained cells counting, we detected significant differences between the numbers of SCN8A+/ankyrin-G+ immunoreactive cells in different groups in acute and chronic period following PISE (two way-ANOVA, F(group)=37.905, P<0.001; F(day)=45.310, P<0.001). The data revealed that both SCN8A and ankyrin-G increased significantly in the CA1 subfield of the rat hippocampus 60 days following pilocarpine induced status epilepticus and co-localized with each other.
电压门控钠通道(VGSC)是神经元兴奋性的重要决定因素,与癫痫的发病机制有关。锚蛋白-G有助于VGSC的分布和调节。在此,我们研究了匹罗卡品诱导的癫痫持续状态(PISE)后大鼠海马角回1(CA1)中两个α亚基SCN8A和SCN1A及其衔接蛋白锚蛋白-G的变化,并与假手术对照组(C1)和空白对照组(C2)进行了比较。PISE后60天检测到SCN8A mRNA显著增加(与C1相比增加41.08%,P<0.001;与C2相比增加30.88%,P=0.011)。在第1天,SCN8A mRNA减少,但与对照组相比未检测到显著变化(单因素方差分析,F=1.232,P=0.276)。在测量蛋白质印迹的光密度后,我们检测到不同组SCN8A蛋白水平之间存在显著差异,但与对照组相比,匹罗卡品处理后第1天和第60天SCN1A蛋白水平之间没有差异。在第60天,与C1和C2相比,PISE组中以内参β-肌动蛋白为对照的锚蛋白-G mRNA的相对拷贝数显著增加(单因素方差分析,F=16.537,P<0.001)。观察到PISE组在PISE后1天和60天蛋白质印迹中锚蛋白-G免疫反应性显著增加,与对照组相比(单因素方差分析,第1天F=24.255,P<0.001;第60天F=29.280,P<0.001)。在分析双染细胞计数后,我们在PISE后的急性期和慢性期不同组中检测到SCN8A+/锚蛋白-G+免疫反应性细胞数量之间存在显著差异(双向方差分析,F(组)=37.905,P<0.001;F(天)=45.310,P<0.001)。数据显示,在匹罗卡品诱导的癫痫持续状态后60天,大鼠海马CA1亚区的SCN8A和锚蛋白-G均显著增加且相互共定位。