首页 | 本学科首页   官方微博 | 高级检索  
检索        

缺血-再灌注损伤对视网膜明胶酶活性的影响
引用本文:陈建丽,蔡小军.缺血-再灌注损伤对视网膜明胶酶活性的影响[J].武汉大学学报(医学版),2005,26(1):25-27,i002.
作者姓名:陈建丽  蔡小军
作者单位:武汉大学中南医院眼科,武汉,430071;武汉大学中南医院眼科,武汉,430071
摘    要:目的 :探讨大鼠视网膜缺血 再灌注 (RIR)损伤时明胶酶A(MMP 2 )和明胶酶B(MMP 9)蛋白的动态变化及意义。方法 :采用前房高压灌注法造成大鼠视网膜缺血 1h ,RIR 0 ,3,2 4 ,4 8和 72h后取材 ,用免疫组化SP法和计算机图像分析系统检测MMP 2 ,9的表达 ,以视网膜电图 (ERG)评估视网膜损伤情况。结果 :对照组和RIR0h视网膜MMP 2 ,9表达极弱 ,阳性染色于RIR 3h增加 ,2 4h达高峰 ,以后逐渐下降。ERGb波波幅于RIR 2 4h达最低 ,之后逐渐恢复。结论 :明胶酶是参与RIR损伤的重要因素。

关 键 词:视网膜缺血-再灌注  明胶酶A  明胶酶B  视网膜电图
文章编号:1671-8852(2005)01-0025-03

Expression of Gelatinase in Retinal Ischemia-reperfusion Injury
Chen Jianli,Cai Xiaojun.Expression of Gelatinase in Retinal Ischemia-reperfusion Injury[J].Medical Journal of Wuhan University,2005,26(1):25-27,i002.
Authors:Chen Jianli  Cai Xiaojun
Institution:Chen Jianli,Cai Xiaojun Department of Ophthalmology,Zhongnan Hospital,Wuhan University,Wuhan 430071,China
Abstract:Objective: To investigate the dynamic changes and significance of matrix metalloproteinases (MMPs), especially gelatinases (MMP-2 and -9) in an experimental retinal ischemia-reperfusion(RIR) injury. Methods: Ischemia injury was induced in adult rats by increasing the pressure of the anterior chamber with perfusion of normal saline. After one hour of ischemia and a varied reperfusion time (0, 3, 24, 48 or 72 h), the rats eyes were enucleated. The levels of MMP-2 and -9 were confirmed by immunohistochemical methods and analyzed by computer-picture analytic system. The retinal damage was assessed by Electroretinogram (ERG) recordings. Results: MMP-2 and -9 positive expression were rarely detected in the control or RIR 0 h specimens, while they increased at RIR 3 h, reached maximal levels at 24 h and dropped gradually afterwards. The b-wave amplitude reduced to the minimum at 24 h and then resumed. Conclusion: Gelatinase may play an important role in the pathomechamism of RIR injury.
Keywords:Retinal Ischemia-reperfusion  Matrix Metalloproteinase  Gelatinase  Electroretinogram
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