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作 者:崔贞玉[1,2] 韩素霞[1] 董晓光[1] 冯磊[1] 常建梅[1] 郭李平[1]
机构地区:[1]新疆医科大学第五附属医院心血管内科,乌鲁木齐830011 [2]安阳市人民医院心内科,河南安阳455000
出 处:《实用药物与临床》2014年第7期811-815,共5页Practical Pharmacy and Clinical Remedies
基 金:国家自然科学基金(81060023)
摘 要:目的探讨大鼠心肌梗死(MI)后心肌组织中AngⅡ的表达与心肌重构的关系,进一步阐明ACE2对大鼠MI后心肌重构的作用机制。方法将32只健康雄性SD大鼠随机分为假手术组(n=8)、MI组(n=8)、氯沙坦小剂量组[MI+10 mg/(kg·d),n=8]和大剂量组[MI+20 mg/(kg·d),n=8],随后将MI组和氯沙坦组大鼠建立心尖部心梗模型。术中检测梗死前后心电图变化情况。术后4周取大鼠心尖部心肌组织,HE染色观察心肌组织病理改变情况,RT-PCR检测心肌内AngⅡ和ACE2的mRNA表达量。结果 HE染色结果显示,MI组与假手术组相比,大鼠心肌细胞肿胀、变形、破裂增多,MI组心肌内AngⅡ的mRNA表达量显著高于假手术组,给予氯沙坦后,表达量呈剂量依赖性下降。MI组心肌内AngⅡ的mRNA表达量显著高于假手术组,给予氯沙坦后,表达量呈剂量依赖性下降。MI组心肌内ACE2的mRNA表达量略高于假手术组,氯沙坦组继续升高,呈剂量依赖性。结论氯沙坦组大鼠ACE2表达量增加,进而通过抑制心肌组织内AngⅡ表达来改善MI后的心室重构。Objective To investigate the effect of ACE2 on myocardial remodeling after myocardial infarction.Methods 32 SD rats were randomly divided into 4 group,sham-operated group(n = 8),myocardial infarction group(MI,n = 8),losartan small-dose group[MI + 10 mg /(kg·d) for 4 weeks,n = 8] and losartan high-dose group[MI +20 mg/(kg·d) for 4 weeks,n =8].Then established the myocardial infarction models,and traced the electrocardiogram in intraoperative.After 4 weeks,observing the pathological changes in myocardium by HE staining,the mRNA expression of AngⅡ and ACE2 in myocardium were detected by RT-PCR.Results Myocyte swelling,deformation and fracture were increased significantly in MI group compared with sham-operated group and were alleviated in losartan group in a dose-dependent.The mRNA expression of AngⅡ significantly upregulated in MI group than in sham-operated group,and downregulated in losartan group in a dose-dependent.The mRNA expressions of ACE2 were slightly higher in MI group than in sham-operated group and further increased in losartan group in a dose-dependent.Conclusion ACE2 can reverse myocardial remodelling by decreasing the expression of AngⅡ in losartan group.
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