首页 | 本学科首页   官方微博 | 高级检索  
     

氯化钆在肝脏缺血再灌注损伤中的保护作用
引用本文:初晨,王勤勇,李建一. 氯化钆在肝脏缺血再灌注损伤中的保护作用[J]. 中国现代普通外科进展, 2012, 15(6): 426-430
作者姓名:初晨  王勤勇  李建一
作者单位:1. 中国医科大学附属第四医院乳腺外科 辽宁沈阳110032
2. 中国医科大学附属盛京医院乳腺外科 辽宁沈阳110000
摘    要:目的:探讨在肝脏缺血再灌注损伤过程中,氯化钆对巨噬细胞的作用以及与细胞凋亡之间的相互关系。方法:将100只雄性Wistar大鼠(7~8周龄,180~220g)随机分为实验组(Gd组)和对照组(tR组),Gd组第1、2天经鼠尾静脉注射O.2%氯化钆溶液(10mg/kg),IR组给予等量生理盐水,第3天建立左半肝缺血再灌注模型,缺血均为60min,按再灌注后O.5、1、6、12和24h时相点采集标本,测定血清ALT、AST、TNF-α水平,测定肝细胞线粒体内MDA含量,TUNEL法测定肝细胞凋亡发生率,免疫组织化学法测定Caspase-3表达,电子显微镜观察细胞凋亡的相关形态学改变。结果:与IR组相比,Gd组再灌注0.5、1、6和12h的ALT水平,6和12h的AST水平均较低(P〈0.05);Gd组各时相点TNF-α水平均低于IR组(P〈O.05);6、12、24hMDA含量低于IR组(P〈O.05);Gd组Caspase-3染色O.5、1、6和12h的IOD值低于lR组(P〈0.05);Gd组TUNEL染色0.5、1、6和12h的IOD值低于IR组(P〈O.05);电子显微镜下Gd组细胞凋亡率少于IR组。结论:肝脏缺血再灌注过程中,氯化钆的保护作用可能是通过抑制巨噬细胞和肝细胞凋亡而实现的。

关 键 词:氯化钆  巨噬细胞  缺血再灌注损伤  肝损伤  Caspase-3  细胞凋亡

Protection of GdCl3 to the hepatic ischemia-reperfusion injury
CHU Chen , WANG Qin-yong , LI Jian-yi. Protection of GdCl3 to the hepatic ischemia-reperfusion injury[J]. Chinese Journal of Current Advances in General Surgery, 2012, 15(6): 426-430
Authors:CHU Chen    WANG Qin-yong    LI Jian-yi
Affiliation:1Department of Breast Surgical,The Fourth Affiliated Hospital of China Medical University(Shenyang 110032,China)2Department of Breast Surgical,Shengjing Hospital of China Medical University(Shenyang 110000,China)
Abstract:Objective: To investigate the relationgship between GdCl3,hepatocyte apoptosis and the macrophage in ischemia reperfusion(I/R) injury.Methods: 100 male Wistar rats(180~220 g,7~8 weeks age) were divided into two groups at random: Gdcl3 exposure group(Gd) and ischemia/reperfusion group(IR).In Gd group,Gdcl3 was injected via the tail vein in the first two days(10 mg/kg),the IR group the same mount of isotonic Na chloridethe was injected.The third day,left branches of portal vein,hepatic artery,hepatic duct were blocked up for 60 min and then opened to establish liver I/R model in rats,In each group,samples were collected in 0.5,1,6,12 and 24 h after reperfusion respectively.The level of ALT,AST,TNF-α and MDA in liver was measured,the incidence of hepatocyt apoptosis was measured by TUNEL,immunohistochemical straining of Caspase-3 was determined with optical microscope,the morphology changes were observed by EM.Results: The level of ALT in 0.5,1,6,12 h,AST measured in 6,12 h after reperfusion in Gd groups were significantly lower than that in IR groups(P<0.05).The level of TNF-α in the Gd groups in all the time were lower than that in the IR groups(P<0.05).The level of MDA measured in 6,12,24 h after reperfusion in Gd groups was totally significantly lower than that in IR groups(P<0.05).The Caspase-3(IOD) measured in 0.5,1,6,12 h time and the express level of TUNEL in 0.5,1,6,12 h after reperfusion in Gd groups were totally significantly lower than that in IR groups corresponding(P<0.05).Conclusion: In the process of ischemia/reperfusion,GdCl3 can decrease the level of ALT,AST and TNF-α,and depress the expression of caspase-3.This protection to the hepatocyte may relate to the inhibiting macrophage and hepatocyte apoptosis.
Keywords:GdCl3·Macrophage·Ischemia/reperfusion injury·Hepatic injury·Caspase-3·Apoptosis
本文献已被 CNKI 维普 万方数据 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号