首页 | 本学科首页   官方微博 | 高级检索  
     

组织纤溶酶原激活剂、肝素抑制人工晶体表面细胞学反应的实验对比研究
引用本文:周唏,李平华. 组织纤溶酶原激活剂、肝素抑制人工晶体表面细胞学反应的实验对比研究[J]. 重庆医学, 2000, 29(5): 396-397
作者姓名:周唏  李平华
作者单位:重庆医科大学附属第一医院眼科,400016
摘    要:目的:探讨tPA(组织纤溶酶原激活剂)、肝素对人工晶体(IOL)表面细胞学反应的抑制作用。方法新西兰大白兔36只,分别tPA、肝素及对照共三组,作晶体囊外摘除及人工晶体植入术。术中分别应用含tPA(25μg/0.2ml)、肝素(100IU/ml)和平衡盐溶液的灌注液。术后1、3、7天和1月各时段取出人工晶体,光学显微镜下观察人工晶体表面的细胞学反应情况,用SAS软件包行方差分析。结果tPA和肝素组

关 键 词:组织纤溶酶原激活剂 肝素 人工晶体 细胞学反应

Experimental Contrast Study of Inhibiting Effects of Tpa VS Heparin on Cellular Response on Intraocular Lens Surface Following Surgery
Zhou Xi,Li Pinghua. Experimental Contrast Study of Inhibiting Effects of Tpa VS Heparin on Cellular Response on Intraocular Lens Surface Following Surgery[J]. Chongqing Medical Journal, 2000, 29(5): 396-397
Authors:Zhou Xi  Li Pinghua
Affiliation:Zhou Xi,Li Pinghua. Department of Ophthalmology,First Affiliated Hospital of Chongqingl Medical University,400016
Abstract:Objective:To investigate the inhibiting effect of tPA (tissue - type plasminogen activator )and heparin on cellular response on the Intraocular Lens (IOL) surface follwing surgery, Methods: 36 New Zealand white rabbits were divided into 3 groups (the tPA, the heparin and the control group), and tPA solution(25ug/0. 2ml)and heparin solution (100U/ml )were locally applied separately during the lens extraction and IOL implantation surgery. The implanted IOLs were extracted from the rabbits' eyes on 1, 3, 7 days and 1 month after surgery, and the cellular response on the IOLs surface was observed under the light microscope. Using SAS software, variance analysis of the data was performed. Results:The degree of the cellular response on the IOLs surface in both tPA group and heparin group was lower than that in the control group, but there was no statistical difference betwween the tPA group and the heparin group. Conclusion: Both tPA and heparin have inhibiting effects on the cellular response on the IOLs surcface following operation in rabbits.
Keywords:tPA HeparinIOL. Cellular response
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