摘要
目的:探讨卡托普利对腹主动脉缩窄大鼠模型心肌Ⅰ和Ⅲ型胶原的改变及其mRNA表达改变的干预作用。方法:模型组根据Doering等方法,用银夹造成腹主动脉部分狭窄(银夹内径0.7 mm)。8周后免疫组织化学法进行Ⅰ型和Ⅲ型胶原染色,并用光密度值作为其含量指标行图像分析,即时PCR扩增后分析并测定胶原mRNA。结果:模型组造模8周时Ⅰ型和Ⅲ型胶原平均光密度及其mRNA表达较假手术组显著升高(P<0.01)。胶原组织化学染色示模型组较假手术组Ⅰ型和Ⅲ型胶原明显增多、增粗及排列紊乱;卡托普利组较模型组胶原明显减少。结论:大鼠腹主动脉缩窄导致反应性纤维化心肌中Ⅰ型和Ⅲ型胶原及其mRNA表达升高;卡托普利延缓甚至逆转心肌纤维化进程。
Objective:To investigate the effect of captopril on collagen type Ⅰ and type Ⅲ and their mRNA expressions in abdominal aortic banding model rats.Methods:Myocardial fibrosis rat model was established by partially banding abdominal aorta with silver clip(inside diameter 0.7 mm)according to Doering′s method.Optical density values of collagen typeⅠand type Ⅲ were measured by immunohistochemistry staining after 8 weeks.The mRNA expressions of collagen typeⅠand type Ⅲ were analyzed by real-time PCR amplification.Results:In the 8th week,compared with sham operation group,the average optical density value and mRNA expressions of collagen type Ⅰ and type Ⅲ were increased obviously in model group(P0.01).The immunohistochemistry staining displayed that collagen type Ⅰand type Ⅲ were deposited,thicken and confused in myocardium stroma;and the quantity of collagen was decreased obviously in model group.Conclusions:The quantity of collagen type Ⅰ and type Ⅲ and the related mRNA expressions were increased in myocardical fibrosis induced by abdominal aortic banding in rats;captopril could delay even reverse the process of myocardial fibrosis.
出处
《蚌埠医学院学报》
CAS
2010年第11期1081-1084,共4页
Journal of Bengbu Medical College
基金
江苏省"六大人才高峰"基金资助项目(2005A2)
关键词
卡托普利
心肌纤维化
Ⅰ型胶原
Ⅲ型胶原
基因表达
captopril
myocardial fibrosis
typeⅠcollagen
type Ⅲ collagen
gene expression