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作 者:孟中良[1] 刘崇敏 邵清[1] 张培建 周斌[1] 邹润龙[1] 庄卓男[4]
机构地区:[1]东南大学医学院附属江阴医院普外科,江苏江阴214400 [2]江苏省江阴中医院外科,江苏江阴214400 [3]扬州大学附属第二临床医院普外科研究室,江苏扬州225000 [4]山东大学齐鲁医院肝胆外科,山东济南250000
出 处:《中国现代普通外科进展》2013年第5期342-346,共5页Chinese Journal of Current Advances in General Surgery
基 金:扬州市科技计划项目(YZ2008042);江苏省卫生厅科研课题(H200770)
摘 要:目的:探讨低氧预适应(HP)对自体原位肝移植大鼠肿瘤坏死因子-α(TNF-α)诱导肝细胞凋亡的保护作用以及可能的机制。方法:采用经门静脉灌注法制备大鼠自体原位肝移植模型,将SD大鼠随机分为正常对照组(NC)、自体肝移植(AT)和AT+低氧预适应(HP)3组。HP组术前用8%氮氧混合气体处理90 min。3组分别于术后1,2,12,24 h处死大鼠取肝脏标本,抽血检测肝功能,RT-PCR检测TNF-α、c-JunmRNA表达水平,透射电子显微镜下观察肝细胞的超微结构变化。结果:术后1、2、12、24h,HP组血清ALT,AST水平较AT组均显著降低,但均高于NC组(P<0.01);HP组各时段TNF-αmR-NA的转录水平较AT组显著降低,但高于NC组(P<0.05);HP组1 h,2 h,12 h时段c-Jun mRNA的转录水平较AT组显著降低,但高于NC组(P<0.05),24 h时段AT、HP、NC组间无显著差异(P>0.05);透射电镜下AT组肝细胞出现典型的凋亡征象,而HP组肝细胞无明显凋亡形态。结论:HP对移植所致的肝脏缺血再灌注损伤有保护作用,其机制可能与减少上游TNF-α表达,抑制JNK信号通路的激活,减轻肝细胞凋亡有关。objeetive: To explore the Impact and significance of hypoxia preconditioning on apoptosis of hepatic cells induced by TNF- α in orthotopic liver autotransplantation in rats. Meth. ods: The model of orthopotic liver transplantation via Portal Vein Perfusion in Rats was established, and the Sprague Dawley rats were randomly divided into the following three groups: normal control (NC)group,autotransplantation (AT)group,and hypoxia preconditioning (HP) group. HP Group was given an 8% oxygen mixed gas for 90 minutes before the operation. Atl,2,12and 24 hours after the operation, the ras were killed and the following tests were conducted: 1)blood was drawn to conduct a chemical examination; 2)RT-PCR observe the expression of TNF- α mRNA and c-Jun mRNA; 3) the ultrastructure changes of hepatocytes were observed under light microscope and transmission electron microscopy.
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