首页> 美国卫生研究院文献>Journal of Korean Medical Science >Myocardial Protective Effect of Tezosentan an Endothelin Receptor Antagonist for Ischemia-Reperfusion Injury in Experimental Heart Failure Models
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Myocardial Protective Effect of Tezosentan an Endothelin Receptor Antagonist for Ischemia-Reperfusion Injury in Experimental Heart Failure Models

机译:内皮素受体拮抗剂Tezosentan在实验性心力衰竭模型中对缺血/再灌注损伤的心肌保护作用

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摘要

The myocardial protective effects of endothelin antagonist in ischemic cardiomyopathy (ICMP), doxorubicin-induced cardiomyopathy (DOX) and pressure-overload hypertrophy by transverse aortic constriction (TAC) models have been predicted to be different. The objective of this experiment, therefore, is to evaluate the myocardial protective effect of tezosentan, an endothelin receptor antagonist, in various experimental heart failure models. Sprague-Dawley rats (6-8 weeks old, 200-300 g) were randomized to three experimental groups (n=30 each): ICMP; DOX; and TAC group. Each of these groups was randomly assigned further to the following subgroups (n=10 each): sham-operated ischemia-reperfusion subgroup (SHAM); tezosentan treated ischemia-reperfusion subgroup (Tezo); and tezosentan non-treated ischemia-reperfusion subgroup (N-Tezo). Total circulatory arrest was induced for 1 hr, followed by 2 hr of reperfusion. The left ventricular developed pressure, peak positive and negative first derivatives, and coronary blood flow were significantly different (P<0.05) among the SHAM, Tezo, and N-Tezo subgroups of the ICMP group at 30 min of reperfusion, but there were no statistically significant differences among the subgroups of the DOX and TAC groups. In conclusion, tezosentan, an endothelin receptor antagonist, showed myocardial protection effects only on the ischemic cardiomyopathy rat model, but not in the non-ischemic heart failure rat models.
机译:内皮素拮抗剂在缺血性心肌病(ICMP),阿霉素诱导的心肌病(DOX)和横动脉主动脉收缩(TAC)模型引起的压力超负荷肥大中的心肌保护作用被预测是不同的。因此,本实验的目的是在各种实验性心力衰竭模型中评估替佐生坦(一种内皮素受体拮抗剂)对心肌的保护作用。将Sprague-Dawley大鼠(6-8周大,200-300 g)随机分为三个实验组(每组n = 30):ICMP; DOX;和TAC小组。这些组中的每组进一步随机分为以下亚组(每组n = 10):假手术缺血再灌注亚组(SHAM);替佐生坦治疗的缺血再灌注亚组(Tezo);和替佐生坦未治疗的缺血再灌注亚组(N-Tezo)。诱导总的循环停止1小时,然后再灌注2小时。 ICMP组的SHAM,Tezo和N-Tezo亚组在再灌注30分钟时,左心室发育压力,正负一阶峰值和负冠状动脉血流量显着不同(P <0.05),但没有DOX和TAC组的亚组之间在统计学上有显着差异。总而言之,内皮素受体拮抗剂替佐生坦仅对缺血性心肌病大鼠模型显示出心肌保护作用,而在非缺血性心力衰竭大鼠模型中则没有显示出心肌保护作用。

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