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作 者:费玲[1] 隋树建[1] 任满意[1] 许复郁[2] 刘伟华[1] 杜贻萌[1]
机构地区:[1]山东大学第二医院心内科,山东济南250033 [2]山东大学第二医院病理科,山东济南250033
出 处:《山东大学学报(医学版)》2007年第2期135-138,共4页Journal of Shandong University:Health Sciences
摘 要:目的:探讨肿瘤坏死因子相关细胞凋亡诱导配体(TRAIL)通过死亡受体-5(DR5)途径诱导的细胞凋亡与动脉粥样硬化(AS)的关系。方法:采用球囊拉伤腹主动脉加高胆固醇饮食的实验方法,建立兔AS模型;血管超声检查明确腹主动脉斑块的形成情况,然后取静脉血和腹主动脉组织,用酶联免疫吸附试验(ELISA)检测AS组及正常组兔血清中可溶性TRAIL(sTRAIL)和可溶性DR5(sDR5)的浓度,免疫组化染色检测AS组及正常组腹主动脉壁TRAIL和DR5的蛋白表达。并比较两组间各项参数的差异。结果:AS组兔血清中sDR5浓度显著高于正常组(P<0.05),而两组兔血清中sTRAIL浓度差异无统计学意义(P>0.05)。AS组兔腹主动脉的TRAIL、DR5蛋白表达强度显著高于正常组(P<0.05),染色呈棕褐色,粗颗粒状,群集于中膜、脂质沉积处和斑块纤维帽处,高倍镜下,棕褐色颗粒主要分布在胞浆和胞核内;正常组兔腹主动脉内膜、中膜也有少量TRAIL、DR5表达,染色呈浅棕色,颗粒细小,分布散在。结论:TRAIL通过死亡受体途径诱导的细胞凋亡对AS的发生和发展起一定的促进作用,TRAIL及其受体DR5可能是AS的重要影响因子。Objective: To explore whether TNF-related apeptosis inducing ligand(TRAIL)and death recep- tor-5(DR5) take part in the occurrence and development of atherosclerosis(AS). Methods: Twenty rabbits were randomly distributed into two groups: the control group and the atherosclerotic group. The experimental atherosclerotic models were made by endothelial injury on the ventro-aorta with a balloon and hyperlipid feeding lasting 12 weeks. The levels of sTRAIL and sDR5 in the sermn were determined by enzyme linked immunoabsorbent assay (ELISA). The proteinum ex- pression of TRAIL and DR5 in the ventro-aortas was detected by immunohistochemical technique. Results: In the course of research, 2 rabbits died. The survival rate was 90%. Till the end of the research, the serum sDR5 in the AS group was more significantly elevated than that in control group ( P 〈 0.05), while the serum sTRAIL in two groups had no significant differences ( P 〉 0.05). The expressions of TRAIL and DR5 in the ventroaortas in the AS group were significantly elevated than those in the control group ( P 〈 0.05). Conclusion: This study suggests that TRAIL and DR5 could promote the occurrence and development of AS. TRAIL and DR5 may be important factors for AS.
关 键 词:动脉硬化 肿瘤坏死因子相关细胞凋亡诱导配体 死亡受体-5 细胞凋亡
分 类 号:R541[医药卫生—心血管疾病] R-332[医药卫生—内科学]
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