TRAIL及其受体与蛛网膜下腔出血后痉挛动脉内皮细胞的凋亡
血管痉挛,,蛛网膜下腔出血;血管痉挛;肿瘤坏死因子相关凋亡诱导配体;凋亡,0引言,1材料和方法,2结果,3讨论
Role of tumor necrosis factorrelated apoptosisinducing ligand(TRAIL)and its receptors in subarachnoid hemorrhage inducing apoptosis in vasospasm artery endothelial cellsWANG Liang1,GAO GuoDong1,ZHAO ZhengWei1,RAO ZhiRen2, QIN HuaiZhou1, JIA Dong1, SHEN Jing2
1Department of Neurosurgery, Tangdu Hospital, Fourth Military Medical University, Xian 710038, China ,2Department of Neurobiology, School of Basic Medicine,Fourth Military Medical University, Xian 710033, China
【Abstract】 AIM: To study the role of tumorrelated apoptosisinducing ligand(TRAIL) and its receporDR4 , receporDR5 in apoptotic endothelial cells of vasospasm artery after subarachnoid hemorrhage. METHODS: Fiftyfour rabbits were used in the present study. The population was randomly divided into three groups: control group, subarachnoid hemorrhage(SAH) group and sham operated group and the groups were sacrificed respectively on preoperation and 0, 2, 4 and 7 d (6 per group). The SAH models were made by doublehemorrhage method. Cerebral vasospasm (CVS) was confirmed by angiogram. TRAIL protein and its receptor DR4 ,DR5 expression positive number and apoptotic cell number were determined using immunohistochemical technique and TdTmediated dUTPbiotin nick end labeling (TUNEL). RESULTS: Angiographic vasospasm began on 0 d and peaked on 2 d to 4 d. In TUNEL studies, control rabbits did not demonstrate apoptosis in endothelial cells of the basilar arteries. CVS rabbits beginning on 0 d, apoptosis were noted in endothelial cells(P<001).In immunohistochemical study, TRAIL ......
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