【摘要】 目的 :探讨caspase 3基因在缺血神经细胞死亡机制中的作用。方法 :采用大鼠大脑中动脉阻塞再灌流模型 (MCAO R) ,运用RT PCR和原位杂交技术观察缺血再灌流后caspase 3mRNA表达的时空分布动态变化 ,结合TUNEL技术观察其与凋亡的关系。结果 :脑缺血 3 0min再灌流 6h和缺血 2h再灌流 1h ,caspase 3mRNA在梗死边缘区的内侧诱导表达 ,并随着缺血时间或再灌流时间的延长而增强。caspase 3基因的表达与凋亡细胞的时空动态变化趋势基本一致。结论 :脑缺血损伤诱导caspase 3基因表达增强 ,caspase 3在介导神经细胞凋亡和缺血性脑损害中起关键作用更多还原

【Abstract】 Aim:Since caspase members have been identified as effectors of apoptosis and caspase-3 is the most key protease,the role of caspase-3 was further explored in neuronal cell death after transient cerebral ischemia.Methods:To determine whether caspase-3 serves to regulate neuronal death after various ischemia/reperfusion time,108 adult Wistar rats were subjected to 30 min or 2 h of transient focal cerebral ischemia induced by intraluminal blockade of the left middle cerebral artery followed by 1～48 h of reperfusion,Caspase-3 mRNA expression was examined by both PT-PCR and in situ hybridization analyses.Terminal deoxynucleotidyltranfer-ase (TdT)-mediated dUTP-flourescein nick end-labeling (TUNEL) staining was performed for the detection of apoptosis.Results:Caspase-3 mRNA was constitutively expressed in rat brain.At 6-48 h after 30 min of occlusion and 1-48 h after 2 h of occlusion,caspase-3 mRNA was markedly induced in the inner boundary zone of the infarction,which became more pronounced with ischemia- or reperfusion-time,with a peak at 24-48 h of reperfusion.The temporal and spatial profile of neuronal apoptosis was consistent with those of caspase-3 gene expression.Conclusion:These observations strongly support a key role for caspase-3 in neuronal apoptosis and ischemic/reperfusion brain injury and suggest that caspase-3 inhibitors may provide a promising opportunity for stroke and other neurological disorders in which apoptosis is prominent.更多还原