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沙土鼠短暂性脑缺血后海马CA1区细胞凋亡及亚低温的影响
引用本文:汪长胜,霍正禄,杨瑞和,龚志锦. 沙土鼠短暂性脑缺血后海马CA1区细胞凋亡及亚低温的影响[J]. 中国危重病急救医学, 2000, 12(12): 726-729
作者姓名:汪长胜  霍正禄  杨瑞和  龚志锦
作者单位:1. 解放军第二六一医院急诊科,北京,100094
2. 第二军医大学长海医院,上海,200433
基金项目:第二军医大学硕士研究生课题基金资助项目(No.19971009)
摘    要:目的:研究沙土鼠短暂性脑缺血后海马CA1区细胞凋亡及亚低温的治疗作用。方法:阻断沙土鼠双侧颈总动脉20分钟造成前脑缺血模型。实验动物被随机分为假手术组、缺血-再灌注组、亚低温治疗组。海马CA1区的迟发性神经元死亡(DND)过程通过序列光镜观察进行研究,原位末端标记(TUNEL)法用来检测死凶的DNA片断。结果:短暂性脑缺血后,海马CA1区锥体神经元于再灌注后2~7日死亡。死亡锥体神经元的序列光镜观察没有发现早期的凋亡样改变,DNA 断化也发生在DND出现之后。亚低温处理动物再灌注后2~7日,海马CA1区缺血性神经元死亡较常温处理动物显著减轻,再灌注后3~7日,海马CA1区DNA片断化也显著减少。结论:缺血后的亚低温治疗产生了神经保护作用,而抑制神经元DNA片断化的出现可能是其保护机制之一。

关 键 词:脑缺血 短暂性 细胞凋亡 亚低温 沙土鼠 病理
修稿时间:2000-06-19

Apoptosis in hippocampal CA1 neurons and effect of moderate hypothermia after transient forebrain ischemia in gerbils
Abstract:Objective To explorethe neuronal apoptosis in the hippocampal CA 1 region and effect of moderate hypothermiaafter transient forebrain ischemia i n gerbils. MethodsTransient forebrain ischemia wasinduced by 20 minutes bilat eral carotid occlusion.All gerbils were randomly divided intosham operation gr oup,ischemiareperfusion group and moderate hypothermia group.Delayedneuronal death (DND) in hippocampal CA1 region was studied by means of sequential lightmicroscopy examination.Fragmented DNA of dead neurons was identified by termina ldeoxynucleotidyl transferase nick endlabeling (TUNEL). ResultsTransient for ebrainischemia induced neuronal death in hippocampal CA1 region on days 27 af terreperfusion.Sequential light microscopic study of dead pyramidal neurons sho wed thatearly chromatin changes of apoptosis were absent and DNA fragmentation occurred after thedevelopment of DND in the CA1 region.Ischemic neuronal injur y was significantly reducedin hypothermic animals on days 27 after reperfusio n compared to the normothermicanimals.TUNEL examination revealed that there wer e much less DNA fragmentations inmoderate hypothemia group than that of ischemi areperfusion group. ConclusionsModeratehypothermia in postischemic period ca n provide protective effects by inhibiting DNAfragmentation in neurons.
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