摘要
目的建立大鼠高肺血流量肺动脉高压模型。方法采取左颈总动脉-颈外静脉分流、左肺动脉结扎以及左颈总动脉-颈外静脉分流联合左肺动脉结扎3种手术方式建立大鼠高肺血流量模型,观察术后8周肺动脉平均压(mPAP)、右心室肥厚指数(RV/LV+S)、肺血管管壁厚度占血管外径的百分比(WT%)和管壁面积占血管总面积的百分比(WA%);以及左颈总动静脉分流联合左肺动脉结扎术后4、8、12周上述指标的变化。结果与对照组比较,左颈总动脉-颈外静脉分流联合左肺动脉结扎在术后8、12周产生明显肺动脉高压,mPAP及RV/LV+S逐渐增加,且差异有统计学意义(P〈0.01),WT%和WA%差异也均有统计学意义(P〈0.01)。结论左颈总动脉.颈外静脉分流联合左肺动脉结扎可建立高肺血流量肺动脉高压模型,且操作简单。
Objective To establish a high-flow type of rat pulmonary hypertension model which can recapitulate clinical characteristics of pulmonary arterial hypertension in congenital heart disease with systemic-to-pulmonary shunts. Methods The animal model established by either left common carotid arter- y-external jugular vein shunts, or ligation of the left pulmonary artery, or combination of the two methods. Changes in mean pulmonary artery pressure (mPAP) , right ventricular hypertrophy index of right ventricle to left ventricle plus interventricular septum ( RV/LV + S) , the ratio of vascular wall thickness to vascular external diameter ( WT% ) and the ratio of vascular wall area to total vascular area ( WA% ) were observed to compare different surgical approaches during postoperative 8 week. The changes of above indexes were also observed following combination of the two methods at 4, 8 and 12 week postoperation. Results As compared with control group, the mPAP and RV/LV + S in combination of shunt and ligation of the left pulmonary artery group were significantly increased at 8th and 12th week ( P 〈 0. 01 ) ; Compared with con- trol group, the WT% and WA% also elevated obviously (P 〈 0. 01 ). Conclusion Combination of shunt and ligation of the left pulmonary artery is an easy and reliable approach to create high flow-induced pulmo- nary arterial hypertension in rats, and can be used to study the pathogenesis of pulmonary arterial hyperten- sion caused by congenital heart diseases.
出处
《中华实验外科杂志》
CAS
CSCD
北大核心
2013年第6期1308-1310,共3页
Chinese Journal of Experimental Surgery
关键词
肺动脉高压
肺血管重构
动
静脉分流
左肺动脉结扎
模型
动物
Pulmonary hypertension
Pulmonary vascular remodeling
Congenital heart dis- ease
Systemic-to-pulmonary shunts
Models, animal