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作 者:高占义[1] 魏月娟[1] 王彦敏[2] 李二娟[1] 张姗[1] 王庆海[3]
机构地区:[1]河北医科大学附属沧州中西医结合临床学院心内科,沧州061000 [2]河北医科大学附属沧州中西医结合临床学院超声科,沧州061000 [3]河北医科大学附属沧州中西医结合临床学院科教科,沧州061000
出 处:《世界中医药》2016年第11期2363-2366,共4页World Chinese Medicine
基 金:河北省中医药管理局"自拟强心汤调控CaN-NFAT信号通路干预慢性心力衰竭的临床研究"(编号:2015287)
摘 要:目的:探讨自拟强心汤对心梗后心力衰竭大鼠心肌舒缩功能的作用机制。方法:采用结扎左冠状动脉法制备大鼠心梗后慢性心力衰竭动物模型;8周后,给予药物灌胃治疗;经治疗4周后,采用通过颈动脉插管测定大鼠血流动力学状态,通过实时荧光定量PCR(FQ-PCR)法和Western Bolt法检测心肌钙调控蛋白肌浆网钙泵(SERCA2a)、雷尼丁受体2(RYR2)mRNA水平及其蛋白表达量。结果:模型组大鼠的心功能显著下降,主要表现在血流动力学参数改变,其中左室舒张末期压(LVEDP)明显升高(P<0.01),左室收缩压(LVSP)、左室上升最大速率(+LVdp/dtmax)及左室下降最大速率(-LVdp/dtmax)绝对值均降低(P<0.05);心肌钙调控蛋白SERCA2a、RYR2 mRNA水平及其蛋白表达量均明显下降(P<0.05)。给予自拟强心汤干预后,能够有效的降低心力衰竭大鼠LVEDP水平(P<0.05),升高LVSP、+LVdp/dtmax、-LVdp/dtmax水平(P<0.01);能够升高心肌钙调控蛋白SERCA2a、RYR2 mRNA及其蛋白表达量的水平(P<0.05)。结论:自拟强心汤能够有效的改善心力衰竭大鼠的心功能,其机制可能与升高心肌钙调控蛋白SERCA2a、RYR2的蛋白表达量,改善钙循环有关。Objective:To clarify myocardial systolic and diastolic function and possible mechanism of Qiangxin Tang on the model of heart failure.Methods:Model of heart failure after myocardial infarction was prepared by left coronary artery ligation .After 8 weeks ,take a lavage treatment every day;After 4 weeks of continuous administration ,cardiac hemodynamics parameters were recor-ded and SERCA2a,RYR2 mRNA level were detected by PCR(FQ-PCR)and SERCA2a,RYR2 protein expression were detected by Western bolt.Results:compared with control group ,cardiac function of model group is lower:hemodynamic parameters LVEDP is increased obviously(P〈0.01),LVSP,+LVdp/dtmax and-LVdp/dtmax absolute values were all lower (P〈0.05),and the calm-odulin SERCA2a and RYR2 mRNA and protein relative expression of model group rats was decreased (P〈0.05).Compared with model group,Qiangxin Tang group could reduce LVEDP levels (P〈0.05),increase LVSP,+LVdp/dtmax and-LVdp/dtmax levels (P〈0.01 ), and the calmodulin SERCA2a and RYR2 mRNA and protein relative expression of Qiangxin Tang were higher.Conclusion:Qiangxin Tang can effectively improves cardiac function in heart failure rats;Its mechanism is related with im-proving calmodulin SERCA2a、RYR2 and improving calcium cycle .
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