首页 | 官方网站   微博 | 高级检索  
     

两个地区东方田鼠基因组RAPD分析比较研究
引用本文:王胜昌  谢建云  邵伟娟 高诚. 两个地区东方田鼠基因组RAPD分析比较研究[J]. 实验动物与比较医学, 2001, 21(1): 26-32
作者姓名:王胜昌  谢建云  邵伟娟 高诚
作者单位:上海第二医科大学附属仁济医院胸心外科,上海,200001
基金项目:中国科学院生物科学与生物技术研究特别支持费课题(财政部专项)“人基因组和后基因组研究角度开发利用”的资助!编号 :KJ95T—0 6
摘    要:为了建立一种与临床上冠脉搭桥手术和经皮腔内冠状动脉成形术(PTCA)等病理过程相似的血管再狭窄模型,探讨血管再构和新内膜形成的机理,及在血管再狭窄中所起的重要作用,我们用不同品系(BALB/cA和C57BL/6J)小鼠的左颈总动脉进行了结扎,在2周和4周后,分别作病理学观察,结果发现两种品系小鼠产生了不同的病理结果,C57BL/6J小鼠有明显的血管狭窄和炎症细胞浸润,而BALB/cA小鼠虽有炎症细胞的浸润,但血管的内膜无炎症细胞浸润,也无血管狭窄表现,结果提示:血管再狭窄是血管再构和新内膜形成的共同原因。

关 键 词:品系 小鼠 血管再狭窄 血管再构 新内膜形成 心血管疾病
文章编号:1004-8448(2001)01-0026-03
修稿时间:2000-07-17

Genomic RAPD Analysis andComparative Study on Fiel d Voles (Microtus Fortis)from Two Regions in China
WANG Shengchang,XIE Jianyun,SHAO Weijuan,GAO Cheng. Genomic RAPD Analysis andComparative Study on Fiel d Voles (Microtus Fortis)from Two Regions in China[J]. Laboratory Animal and Comparative Medicine, 2001, 21(1): 26-32
Authors:WANG Shengchang  XIE Jianyun  SHAO Weijuan  GAO Cheng
Abstract:Restenosis is one of the major limitations of PTCA and CABG, it can be assumed as a combination of neointima formation and arterial remodeling in response to injury. We recently established model with mice BALB/cA and C57BL/6J. After ligation of the left common carotid artery just proximal to the bifurcation resulting in 90% reduction of lumen area by a combination of intimal hyperplasia together with decreased diameter. In this study, neointima formation in C57BL/6J mice and BALB/cA mice was compared. Two and four weeks after the ligation, leukocyte infiltration was observed in the developing neointima, a 90% reduction of luminal area was observed in C57BL/6J; While in BALB/cA no neointima formation was observed. Conclusion: Vascular remodeling with neointima formation was the cause of restenosis, presumably by mediating leukocyte recruitment and the interaction between platelets and leukocytes.
Keywords:Restenosis  Remodeling  Neointima formation
本文献已被 CNKI 维普 万方数据 等数据库收录!
点击此处可从《实验动物与比较医学》浏览原始摘要信息
点击此处可从《实验动物与比较医学》下载全文
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-23

京公网安备 11010802026262号