李建军, 张晓雷, 王小姗, 孙琦, 张玲如. 银杏叶提取物(EGb761)对鼠脑缺血半暗带神经细胞凋亡及超微结构的影响[J]. 蚌埠医科大学学报, 2008, 33(4): 400-402.
    引用本文: 李建军, 张晓雷, 王小姗, 孙琦, 张玲如. 银杏叶提取物(EGb761)对鼠脑缺血半暗带神经细胞凋亡及超微结构的影响[J]. 蚌埠医科大学学报, 2008, 33(4): 400-402.
    LI Jian-jun, ZHANG Xiao-Lei, WANG Xiao-shan, SUN Qi, ZHANG Ling-ru. Influence of Ginkgo Biloba Extract on neural cell apoptosis and ultrastructure in ischemic penumbra after cerebral ischemia/reperfusion in rats[J]. Journal of Bengbu Medical University, 2008, 33(4): 400-402.
    Citation: LI Jian-jun, ZHANG Xiao-Lei, WANG Xiao-shan, SUN Qi, ZHANG Ling-ru. Influence of Ginkgo Biloba Extract on neural cell apoptosis and ultrastructure in ischemic penumbra after cerebral ischemia/reperfusion in rats[J]. Journal of Bengbu Medical University, 2008, 33(4): 400-402.

    银杏叶提取物(EGb761)对鼠脑缺血半暗带神经细胞凋亡及超微结构的影响

    Influence of Ginkgo Biloba Extract on neural cell apoptosis and ultrastructure in ischemic penumbra after cerebral ischemia/reperfusion in rats

    • 摘要: 目的:探讨银杏叶提取物(EGb761)对鼠脑缺血半暗带神经细胞凋亡及细胞超微结构的影响。方法:雄性Wistar大鼠30只,随机分为假手术组、对照组(包括缺血90 min和缺血90 min再灌注12 h两个亚组)、治疗组(亦包括缺血90 min和缺血90 min再灌注12 h两个亚组),每组6只。治疗组于缺血前和缺血后即刻经腹腔注射EGb761溶液(每次20 mg/kg),假手术组和对照组均于相同时限腹腔注射等容量的生理盐水。建立大鼠大脑中动脉闭塞(MCAO)/再灌注模型。采用原位末端标记法,观察各组鼠脑缺血半暗带神经细胞凋亡,并结合电镜观察缺血神经细胞超微结构的改变。结果:对照组缺血90 min再灌注12 h缺血半暗带可见大量凋亡细胞,凋亡细胞计数为21.2±3.8,较药物治疗组缺血90 min再灌注12 h缺血的9.1±2.3显著增加(P<0.01)。对照组缺血90 min再灌注12 h鼠脑组织电镜检查可见神经元细胞核染色质边聚,呈团块状,线粒体可见絮状结构改变;相同时限药物治疗组脑组织神经元细胞核染色质分布比较均匀,胞质内线粒体及其它细胞器基本正常。结论:血小板活化因子受体拮抗剂EGb761具有显著的缺血后脑保护作用。

       

      Abstract: Objective: To investigate the influence of Ginkgo Biloba Extract on neural cell apoptosis and urtra micro-structure of neural cells in cerebral ischemic penumbra after cerebral ischemia/reperfusion in rats.Methods: Thirty male Wister rats were randomly divided into sham-operation group(n=6),control group(n=6) and treatment group(n=6).The treatment group were injected intraperitoneally Ginkgo Biloba Extract 761(20 mg/kg) before and after middle cerebral artery occlusion;the sham-operation group and control group were injected normal saline(20 mg/kg).Animal models were established by middle cerebral artery occlusion.The number of nerual cell apoptosis was measured by thymidine/deoxythymidine mediated dexoy UTP-biotin nick and labeling(TUNEL),and the changes of ultra micro-structure of neural cells were observed by electromicroscope.Results: The number of neural cell apoptosis was 21.2±3.8 in control group after ischemia 90 min/reperfusion 12 h,versus 9.1±2.3 in Ginkgo Biloba Extract-treated group after ischemia 90 min/reperfusion 12 h,the difference was significant(P<0.01).The neuron apoptotic cells were observed by their fragmented nuclei condensed chromatin,fragmented or condensed cytoplasm and floccule of mitochondrion in the control group after ischemia 90 min/reperfusion 12 h;whereas the distribution of chromatin was well-proportioned,and normal mitochondrion and other organelle were observed in the Ginkgo Biloba Extract-treated group.Conclusions: As platelet-activating factor receptor antagonists,Ginkgo Biloba Extract has remarkable neuroprotective effect.

       

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