首页 | 本学科首页   官方微博 | 高级检索  
     

尼莫地平预处理和梗塞后治疗对大鼠脑缺血损伤保护作用的比较研究
引用本文:胡明,刘昌勤,冯作化. 尼莫地平预处理和梗塞后治疗对大鼠脑缺血损伤保护作用的比较研究[J]. 脑与神经疾病杂志, 2005, 13(3): 182-185
作者姓名:胡明  刘昌勤  冯作化
作者单位:430022,武汉,华中科技大学同济医学院附属协和医院神经内科;华中科技大学同济医学院分子生物学系
摘    要:目的:探讨尼莫地平(Nimodipine,NIM)预处理和梗塞后给药对脑缺血区神经元保护作用的差异。方法:采用线栓法建立大鼠脑缺血模型;尼莫地平给药方式为单预处理、单梗塞后给药或预处理+梗塞后治疗;红四氮唑(TTC) 染色测定脑梗塞体积百分比;逆转录聚合酶链式反应(RT-PCR)法测定动物海马组织中Caspase-3 mRNA和Bcl-2 mR NA的相对表达量。结果:尼莫地平预处理+梗塞后治疗组、单预处理组及单治疗组的脑梗塞体积百分比均显著小于对照组,而前三组相比,预处理+梗塞后治疗组的脑梗塞体积百分比小于单预处理组及单治疗组,但单预处理组及单治疗组间无明显差异。Caspase-3 mRNA表达量为对照组最高,单治疗组次之,单预处理组又次,预处理+梗塞后治疗组最低;Bcl-2mRNA在各组的表达量与Caspase-3 mRNA相反。结论:尼莫地平预处理+梗塞后治疗的方式对缺血神经元的保护作用最强,单预处理次之,而单梗塞后治疗的保护作用最弱。

关 键 词:尼莫地平  脑缺血:预处理
文章编号:1006-351X(2005)03-0182-04
修稿时间:2005-02-25

A Study of the Protective Role of Pre-treated or Treated after Ischemia Onset with Nimodipine on Rats Cerebral Ischemia Model
HU Ming,LIU Chang-qin,FENG Zuo-hua. A Study of the Protective Role of Pre-treated or Treated after Ischemia Onset with Nimodipine on Rats Cerebral Ischemia Model[J]. Journal of Brain and Nervous Diseases, 2005, 13(3): 182-185
Authors:HU Ming  LIU Chang-qin  FENG Zuo-hua
Affiliation:HU Ming,LIU Chang-Qin,FENG Zuo-Hua. Department of Neurology,Union Hospital Tongfi Medical College. Huazhong University of Science and Technology,Wuhan,430030,China
Abstract:Objective: To study the differences of the protective role between pre-treated and treated after ischemia onset with Nimodipine on the neurons in cerebral ischemia areas. Methods:The cerebral ischemic model of rat was made by occluding left middle cerebral artery according to Nagasawy and Zea Longa improvement method. The rats were pre-treated, treaded after ischemia onset or pre-treated plus treaded after ischemia with Nimodipine. The percentage of the infarction volume was calculated by red tetrazoline (ITC) pigmentation. The level of Caspase-3 and Bcl-2 mRNA were measured by RT-PCR method. Results: The percentage of the cerebral infarction volume of pre-treated, treated after ischemia and pre-treated plus treaded after ischemia with Nimodipine was significant lower than that of control, and in the above three groups, the infarction percentage of the last group was lower than the anterior two. However, there was no significant difference between the percentage of pre-treated group and the one of treated after ischemia. The level of Caspase-3 mRNA was the highest in control group, and the expression was lower in treated after ischemia group, pre-treated group and pre-treated plus treated after ischemia group in turn. The level of Bcl-2 mRNA was reversed in the four groups. Conclusion: There was stronger protective effects of pre-treated plus treated after ischemia with Nimodipine than pre-treated or treated after ischemia.
Keywords:Nimodipine   cerebral ischemia   pre-treating
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