首页 | 官方网站   微博 | 高级检索  
     

转化生长因子-β1及其胞内信号通路SMADs在大鼠心肌肥厚中的作用
引用本文:黄俊,覃国辉,马业新.转化生长因子-β1及其胞内信号通路SMADs在大鼠心肌肥厚中的作用[J].中国病理生理杂志,2004,20(9):1601-1604.
作者姓名:黄俊  覃国辉  马业新
作者单位:华中科技大学同济医学院附属同济医院心内科, 湖北 武汉 430030
摘    要:目的:研究SMADs信号通路在大鼠心肌肥厚中的作用。方法:结扎大鼠腹主动脉复制心肌肥厚模型,检测术后不同时间点的大鼠左心室重量指数(LVMI),RT-PCR法检测肥厚左室心肌中转化生长因子β1(TGF-β1)及Smad 2、3、7的mRNA表达。结果:与对照组比较,手术组术后3 d LVMI开始上升并持续至4周,心肌组织中TGF-β1及Smad 2、3的mRNA表达术后3 d也开始上升并持续至4周,术后第2周为表达的高峰(P<0.01)。Smad 7 mRNA术后3 d上升,1周时为其高峰,2周后表达下降。结论:信号蛋白Smad 2、3、7参与了腹主动脉结扎诱导的大鼠心肌肥厚病理过程。

关 键 词:心肌肥厚  转化生长因子β  信号转导  
文章编号:1000-4718(2004)09-1601-04
收稿时间:2003-2-24
修稿时间:2003-5-23

Roles of TGF- β1 and singal protein SMADs in rat myocardial hypertrophy
HUANG Jun,QIN Guo-hui,MA Ye-xin.Roles of TGF- β1 and singal protein SMADs in rat myocardial hypertrophy[J].Chinese Journal of Pathophysiology,2004,20(9):1601-1604.
Authors:HUANG Jun  QIN Guo-hui  MA Ye-xin
Affiliation:Department of Cardiology, Tongji Hospital of Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030, China
Abstract:AIM: To investigate the role of SMADs singal pathway in rat myocardial hypertrophy. METHODS: The rat model of myocardial hypertrophy was produced by constriction of the abdominal aorta. The wet left vertricular/body weight ratio (LVMI) was measured. The expression of TGF-beta l and Smad 2, 3, 7 mRNA were assessed by RT-PCR. RESULTS: The LVMI and the expression of TGF-beta l and Smad 2, 3, 7 mRNA in cardiomyothy were increased in 3 day after the operation and continued at last 4 weeks. The peak expression of TGF-beta l and Smad 2, 3, 7 mRNA was in 2 weeks after operation. The expression of Smad 7 was increased in 3 days after operation, but the peak was in 1 week after operation, then decreased. CONCLUSION: The signal protein Smad 2, 3, 7 are involved in the progress of rat myocardial hypertrophy produced by constriction of abdominal aorta.
Keywords:Myocardial hypertrophy  Transforming growth factor beta  Signal transduction
本文献已被 CNKI 万方数据 等数据库收录!
点击此处可从《中国病理生理杂志》浏览原始摘要信息
点击此处可从《中国病理生理杂志》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