通络药物对心梗后心衰大鼠非梗死区心肌纤维化的影响

被引:8
作者
李佳彧 [1 ]
李佳睿 [2 ]
马丕勇 [1 ]
杨萍 [1 ]
倪维华 [3 ]
机构
[1] 吉林大学中日联谊医院
[2] 吉林省肿瘤医院
[3] 吉林大学白求恩医学院
关键词
心衰; 芪苈强心; 胶原-I; 非梗死区;
D O I
10.13241/j.cnki.pmb.2011.18.013
中图分类号
R285.5 [中药实验药理];
学科分类号
100806 [中药药理学];
摘要
目的:探讨不同剂量芪苈强心胶囊对心衰模型大鼠非梗死区胶原蛋白分子表达的影响。方法:将通过结扎冠状动脉左前降支并饲养4周的56只心衰模型鼠随机分成4组:心衰对照组(MI-C)、转换酶抑制剂雷米普利治疗组(MI-R,10 mg/kg.d)、芪苈强心小剂量组(MI-S,0.25 g/kg.d)以及芪苈强心大剂量组(MI-L,1.0 g/kg.d)。同步药物干预4周后,ELISA法检测Ang II水平、RT-PCR检测非梗死区胶原-I mRNA。结果:血清中Ang II的浓度:与心力衰竭对照组比较,假手术组、雷米普利组、大剂量芪苈强心组和小剂量芪苈强心组均明显降低(P<0.05)。其中,大剂量芪苈强心组比雷米普利组明显减低,差异具显著性(P<0.05);而小剂量芪苈强心组与雷米普利组水平接近,差异无显著性(P<0.05)。非梗死区胶原-I mRNA的表达:与心衰对照组比较,假手术组、雷米普利组、大剂量芪苈强心组,小剂量芪苈强心组表达均下调,差别具显著性(P<0.05);大剂量芪苈强心组与雷米普利组接近,差别无显著性(P>0.05);小剂量芪苈强心组高于大剂量芪苈强心和雷米普利组,差别具有显著性(P<0.05)。结论:芪苈强心胶囊能够明显地减少心梗后心衰非梗死区胶原分子的合成,并具有明显的剂量依赖性。
引用
收藏
页码:3431 / 3433+3464 +3464
页数:4
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