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黄芩苷对海人酸致痫小鼠海马x染色体连锁凋亡抑制蛋白表达的影响
引用本文:廖正俭,梁日生,石松生,王春华,杨卫忠.黄芩苷对海人酸致痫小鼠海马x染色体连锁凋亡抑制蛋白表达的影响[J].国际神经病学神经外科学杂志,2013(5):423-426.
作者姓名:廖正俭  梁日生  石松生  王春华  杨卫忠
作者单位:[1]福建医科大学协和临床医学院,福建省福州市350001 [2]福建医科大学附属协和医院神经外科,福建省福州市350001
基金项目:福建省自然科学基金(2011J01175)
摘    要:目的探讨黄芩苷对海人酸诱导的小鼠癫痫持续状态后海马组织x染色体连锁凋亡抑制蛋白(XIAP)表达的影响。方法将90只ICR雄性小鼠随机分为对照组、癫痫持续状态(sE)组、黄芩苷治疗组,每组30只;采用侧脑室注入海人酸建立小鼠癫痫持续状态模型。通过苏木素一伊红(HE)染色观察黄芩苷对小鼠癫痫持续状态后海马神经细胞的形态学改变;应用免疫组化和Westernblot方法检测小鼠海马组织中XIAP的表达量。结果黄芩苷明显改善sE后小鼠海马组织的病理形态学,海马CA3区XIAP在sE后6h起逐渐增加,12h达高峰,24h有所下降;与对照组比较,差异有统计学意义(P〈0.01)。黄芩苷治疗组海马XIAP蛋白表达在6h、12h和24h均高于sE组(P〈0.05)。结论黄芩苷对小鼠癫痫持续状态后海马神经细胞的保护作用,可能与其促进XIAP的表达有关。

关 键 词:癫痫  黄芩苷  染色体连锁凋亡抑制蛋白  神经保护  小鼠

Effect of baicalin on expression of X-linked inhibitor of apoptosis protein in hippocampus of mice after kainic acid-induced status epilepticus
LIAO Zheng-Jian,LIANG Ri-Sheng,SHI Song-Sheng,WANG Chun-Hua,YANG Wei-Zhong.Effect of baicalin on expression of X-linked inhibitor of apoptosis protein in hippocampus of mice after kainic acid-induced status epilepticus[J].Journal of International Neurology and Neurosurgery,2013(5):423-426.
Authors:LIAO Zheng-Jian  LIANG Ri-Sheng  SHI Song-Sheng  WANG Chun-Hua  YANG Wei-Zhong
Institution:. (Union Clinical College, Fujian Medical University, Fuzhou 350001, China)
Abstract:Objective To investigate the effect of baicalin on the expression of X-linked inhibitor of apoptosis protein (XIAP) in the hippocampus of mice after kainic acid-induced status epilepticus (SE). Methods Ninety male ICR mice were randomly and equally divided into three groups : control, SE, and baicalin treatment groups. A mouse model of SE was established by injection of 0.1 p~g/ 5 txl kainic acid into the lateral ventricle. HE staining was used to observe the pathological changes in hippocampal CA1 and CA3 re- gions after SE; the expression of XIAP was measured by immunohistochemistry and Western blot. Results Baicalin significantly re- duced the pathological changes in the hippocampus of mice after SE. In the SE group, the expression of XIAP in hippocampal CA1 and CA3 regions increased gradually since 6 hrs after SE, reached the peak level at 12 hrs, and decreased at 24 hrs; the expression of XI- AP was significantly higher in the SE group than in the control group at the three time points (P 〈 0.01 ) ; compared with the SE group, the baicalin treatment group had significantly higher expression of XIAP in hippocampal CA1 and CA3 regions at 6, 12, and 24 hrs (P 〈 0.05). Conclusions Baicalin has a protective effect on the hippocampal neurons in mice after SE, which might be associated with the up-regulated expression of XIAP.
Keywords:Epilepsy  Baicalin  X-linked inhibitor of apoptosis protein  Neuroprotection  mice
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