人参皂甙Rd对匹罗卡品致癎大鼠模型中netrin-1表达及神经元凋亡的影响  

Effects of ginsenoside-Rd on expression levels of netrin-1 and neuron apoptosis in epilepsy model

作　　者：郑佳丽[1] 杨金升[2] 刘学娟[1] 马亚杰[1] 

机构地区：[1]兰州大学第二临床医学院,730000 [2]兰州军区兰州总医院神经内科

出　　处：《中华老年心脑血管病杂志》2011年第5期460-462,共3页Chinese Journal of Geriatric Heart,Brain and Vessel Diseases

摘　　要：目的探讨人参皂甙Rd(GSRd)对大鼠癫癎持续状态后齿状回netrin-1表达及海马神经元凋亡的影响。方法健康Wistar大鼠30只,随机分为颞叶癫癎组、GSRd组和对照组,每组10只。氯化锂-匹罗卡品建立大鼠颞叶癫癎模型,采用免疫组织化学法及TUNEL法观察颞叶癫癎组、GSRd组和对照组齿状回netrin-1蛋白表达及海马神经元凋亡细胞数情况。结果与对照组比较,颞叶癫癎组大鼠30 d齿状回netrin 1蛋白表达明显增高,海马CA3区TUNEL阳性细胞数在癫癎持续状态后7 d明显增高,差异有统计学意义(P<0.05);与颞叶癫癎组比较,GSRd组大鼠30 d齿状回nctrin l蛋白表达明显降低,海马CA3区TUNEL阳性细胞数在癫癎持续状态后7 d明显降低,差异有统计学意义(P<0.05)。结论 GSRd可能通过下调netrin 1的表达,并使神经元凋亡数目减少,从而发挥对神经元的保护作用。Objective To investigate the effects of ginsenoside-Rd（GSRd） on the expression levels of netrin-1 and neuron apoptosis in the rat hippocampus after lithium-pilocarpine induced epilepsy. Methods Thirty Wistar rats were randomly divided into the NS control group,temporal lobe epilepsy（TLE） group and GSRd group. The TLE animal model was established using lithium-piloearpine. Netrin-I proteins were detected with immunohistochemieal method. The neuron apoptosis was observed with TdT-mediated dUTP nick end labeling（TUNEL） method. Results The ex- pression of netrin-1 in GSRd group was notably lower than that of TLE group （P 〈 0.05）. The TUNEL positive cells in hippoeampus CA3 of TLE group were more than those of NS control group （P 〈 0.05）. TUNEL positive cells in TLE group were significantly more than those in NS control group （P 〈 0.05）. TUNEL positive cells in GSRd treated group significantly decreased as compared with TLE group （P 〈 0.05）. Conclusions GSRd may serve as an effective agent for curing the brain damage after TLE in vivp . The mechanism of protecting the neuron may include downregulating the expression of netrin-1 and reducing the number of apoptotic neurons.

关 键 词：人参皂甙类 癫痫 神经元 海马 细胞凋亡 氯化锂 模型 动物 

分 类 号：R285[医药卫生—中药学]