首页> 美国卫生研究院文献>Evidence-based Complementary and Alternative Medicine : eCAM >Tongxinluo Improves Cardiac Function and Ameliorates Ventricular Remodeling in Mice Model of Myocardial Infarction through Enhancing Angiogenesis
【2h】

Tongxinluo Improves Cardiac Function and Ameliorates Ventricular Remodeling in Mice Model of Myocardial Infarction through Enhancing Angiogenesis

机译:通心络通过增强血管新生作用改善心肌梗死小鼠模型的心脏功能并改善其心室重构

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Background. Myocardial infarction (MI) is a major cause of morbidity and mortality in the world. Tongxinluo (TXL) is a traditional Chinese compound prescription which has cardioprotective functions. The present study was aimed to determine the effect of TXL on postischemic cardiac dysfunction and cardiac remodeling and to elucidate the underlying mechanisms. Methods and Results. MI was performed by ligation of left anterior descending coronary artery (LAD) in male adult mice. Mice were randomly divided into four groups: (1) sham group (Sham); (2) MI-control group (Control); (3) MI-low dose TXL group (TXL-L); and (4) MI-high dose TXL (TXL-H) group. Compared with the control group, TXL treatment restored cardiac function, increased revascularization, attenuated cardiomyocyte apoptosis, and reduced interstitial fibrosis. TXL treatment increased the phosphorylation of Akt, extracellular signal regulated kinase (ERK), and endothelial nitric oxide synthase (eNOS); the expression of phosphatidylinositol3-kinase (PI3K), hypoxia-inducible factors 1α (HIF-1α), and vascular endothelial growth factor (VEGF); and the DNA binding activity of HIF-1α after MI. Conclusion. TXL may improve cardiac function and ameliorate cardiac remodeling by increasing neovascularization through enhancing the phosphorylation of Akt and ERK, the expression and activity of HIF-1α, and the protein level of VEGF and p-eNOS.
机译:背景。心肌梗塞(MI)是世界上发病率和死亡率的主要原因。通心络(TXL)是具有心脏保护功能的中药复方。本研究旨在确定TXL对缺血后心脏功能障碍和心脏重塑的影响,并阐明其潜在机制。方法和结果。通过结扎雄性成年小鼠左前降支冠状动脉(LAD)进行MI。小鼠随机分为四组:(1)假手术组(Sham); (2)MI控制组(Control); (3)MI低剂量TXL组(TXL-L); (4)MI高剂量TXL(TXL-H)组。与对照组相比,TXL治疗可恢复心脏功能,增加血运重建,减少心肌细胞凋亡并减少间质纤维化。 TXL处理可增加Akt的磷酸化,细胞外信号调节激酶(ERK)和内皮型一氧化氮合酶(eNOS);磷脂酰肌醇3-激酶(PI3K),缺氧诱导因子1α(HIF-1α)和血管内皮生长因子(VEGF)的表达; MI后HIF-1α的DNA结合活性结论。 TXL可以通过增强Akt和ERK的磷酸化,HIF-1α的表达和活性以及VEGF和p-eNOS的蛋白水平来增强新血管形成,从而改善心脏功能并改善心脏重塑。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

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