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机构地区:[1]中国中医科学院广安门医院,北京100053 [2]北京中医药大学,北京100029
出 处:《中国实验方剂学杂志》2014年第10期183-187,共5页Chinese Journal of Experimental Traditional Medical Formulae
基 金:国家自然科学基金项目(81273945)
摘 要:目的:探讨芪苈强心胶囊对改善慢性心衰(CHF)大鼠的心功能及水通道蛋白-2(AQP-2)表达的影响及其改善慢性心力衰竭水代谢紊乱的机制。方法:结扎冠脉左前降支,建立急性心肌梗死(AMI)模型,存活者随机分为模型组(等体积水),芪苈强心组(1 g·kg-1·d-1),缬沙坦组(10 mg·kg-1·d-1),另设假手术组(等体积水)。给药4周后,应用超声心动图检测大鼠的心功能;并通过免疫组化和Western blotting检测大鼠肾集合管AQP-2表达。结果:与假手术组相比,模型组左心室舒张末期内径(LVEDD)和左心室舒张末期内径(LVESD)明显增加,射血分数(EF)和短轴缩短分数(FS)显著降低(P<0.05),证实造模成功;与模型组相比,芪苈强心组和缬沙坦组LVEDD和LVESD均明显减小,EF和FS均显著升高(P<0.05);芪苈强心组与缬沙坦组比较,差异无统计学意义;与假手术组相比,模型组AQP-2表达水平显著升高(P<0.05);与模型组相比,芪苈强心和缬沙坦组AQP-2表达均显著降低(P<0.05),两组AQP-2表达比较,差异亦无统计学意义。结论:芪苈强心可有效下调AQP-2的表达水平,调节由慢性心衰导致的水代谢紊乱,改善水肿症状、从而提高慢性心衰患者的生存质量。Objective: To study Qili Qiangxin capsule(QL)' s function in improves the chronic heart failure rats' cardiac function and its' influence in the aquaporin-2 Water channel expression, then discuss benefit of how Qili Qiangxin therapies for disorders that chronic heart failure rats' aberrant water movement. Method: The proximal left anterior descending branch (LAD) of coronary artery was ligated using a terylene suture in acute myocardial infarction(AMI) rats, after building AMI model successfully , survivors were randomly divided into four groups, model group (equal volume of water), QL group (1g·kg^-1·d-1), valsartan group (10 mg·kg^-1·d^-1), sham-operated group (equal volume of water) .Drug intervention four weeks ,then detection of related indicators. Echocardiography and the expressions of aquaporin-2 were detected by the method of immunohistochemistry and western blotting were assessed 4 weeks after the drug therapy. Result: Compared with the sham-operated group, the left ventricular end-diastolic dimension(LVEDD) and left ventricular end-systolic dimension(LVESD) of model group is significantly increased, ejection fractions(EF) and factional shortening(FS) was significantly lower (P〈0.05); compared with model group, QL group LVEDD and LVESD is significantly reduced , EF and FS were significantly higher (P〈0.05). There was no significant difference between QL group and valsartan group; compared with the sham-operated group , the aquaporin-2 water channel expression levels were significantly higher in model group(P〈0.05); compared with the model group, the AQP-2 expression were reduced to varying degrees in QL and valsartan group (P〈0.05); while there was no significant difference between QL group and valsartan group. Conclusion: QL can be effectively reduced AQP-2 expression levels, improve chronic heart failure caused by the water metabolism, elimination of edema symptoms, thereby improving the quality of life in patients
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