...
首页> 外文期刊>Life sciences >The protective effect of ApolipoproteinA-I on myocardial ischemia-reperfusion injury in rats.
【24h】

The protective effect of ApolipoproteinA-I on myocardial ischemia-reperfusion injury in rats.

机译:载脂蛋白A-1对大鼠心肌缺血再灌注损伤的保护作用。

获取原文
获取原文并翻译 | 示例

摘要

It is well established that reperfusion of heart is the optimal method for salvaging ischemic myocardium, however, the success of this therapy could be limited by reperfusion injury, which is involved in inflammatory responses. High density lipoprotein (HDL) has an anti-inflammatory function and can protect the heart from ischemia-reperfusion (I/R) injury. In this study, we investigated the cardioprotective role of apolipoprotein A-I (ApoA-I), the major apolipoprotein of HDL, in I/R injury. Using rats subjected to myocardial I/R by ligation of left anterior descending coronary artery (LAD), we found that administration of ApoA-I (20 mg/kg, iv) before the onset of reperfusion of myocardial infarction can significantly reduce serum creatine kinase (CK) levels (62.1+/-13.8%, p<0.01) and heart TNF-alpha as well as IL-6 levels, compared with saline controls (40.4+/-14.7%, 44+/-9.8%, p<0.01 respectively). Moreover, ApoA-I treatment suppresses the expression of ICAM-1 on endothelium, thus diminishing neutrophil adherence, transendothelial migration, and the subsequent myocyte injury. We concluded that ApoA-I could effectively protect rat heart from I/R injury.
机译:众所周知,心脏的再灌注是挽救缺血性心肌的最佳方法,但是,该疗法的成功可能受到与炎症反应有关的再灌注损伤的限制。高密度脂蛋白(HDL)具有抗炎功能,可以保护心脏免受缺血再灌注(I / R)的伤害。在这项研究中,我们调查了载脂蛋白A-I(ApoA-I)(HDL的主要载脂蛋白)在I / R损伤中的心脏保护作用。使用结扎左前降支冠状动脉(LAD)进行心肌I / R的大鼠,我们发现在心肌梗塞再灌注开始前给予ApoA-I(20 mg / kg,iv)可以显着降低血清肌酸激酶(CK)水平(62.1 +/- 13.8%,p <0.01)和心脏TNF-alpha以及IL-6水平,而盐水对照组(40.4 +/- 14.7%,44 +/- 9.8%,p < 0.01)。此外,ApoA-I处理可抑制ICAM-1在内皮细胞上的表达,从而减少中性粒细胞的粘附,跨内皮迁移以及随后的心肌细胞损伤。我们得出的结论是,ApoA-I可以有效保护大鼠心脏免受I / R损伤。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号