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首页> 外文期刊>Journal of Pharmacopuncture >Teucrium polium L. Improved Heart Function and Inhibited Myocardial Apoptosis in Isolated Rat Heart Following Ischemia-Reperfusion Injury
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Teucrium polium L. Improved Heart Function and Inhibited Myocardial Apoptosis in Isolated Rat Heart Following Ischemia-Reperfusion Injury

机译:Teucrium polium L.改善缺血再灌注损伤后离体大鼠心脏的心脏功能并抑制其心肌细胞凋亡

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Objectives: Myocardial reperfusion is the only logical cure for ischemic heart disease. However, ischemic-reperfusion (I/R) injury is one of the underlying factors facilitating and accelerating the apoptosis in the myocardium. This study set to investigate the impact of Teucrium polium (TP) hydro-alcoholic extract on I/R induced apoptosis in the isolated rat heart. Methods: Isolated rat hearts were classified into six groups. The control samples were subjected to 80 min of perfusion with Krebs-Henseleit bicarbonate (KHB) buffer; in control-ischemia group, after primary perfusion (20 min) the hearts were exposed to global ischemia (20 min) and reperfusion (40 min). Pretreated groups were perfused with $500{mu}M$ of vitamin C and various TP concentrations (0.5, 1, 2 mg/ml) for 20 min, and then the hearts were exposed to ischemia and reperfusion for 20 min and 40 min, respectively. Cardiodynamic parameters including rate pressure product (RPP), heart rate (HR), the maximum up/down rate of left ventricular pressure ( ${pm}dp/dt$ ), left ventricular developed pressure (LVDP), and coronary artery flow (CF) were achieved from Lab Chart software data. The Bax and BCl-2 gene expressions were measured in heart samples. Results: Hearts treated with TP extract and vit C represented a meaningful improvement in cardiac contractile function and CF. The overexpression of Bcl-2, downregulation of Bax, and improvement of apoptotic index (Bax/Bcl-2) were observed in pretreated TP extract and vit C hearts. Conclusion: The TP extract was found to ameliorate the cardiac function in the reperfused myocardium. Also, it can hinder apoptotic pathways causing cardioprotection.
机译:目的:心肌再灌注是缺血性心脏病的唯一合理治疗方法。然而,缺血再灌注(I / R)损伤是促进和加速心肌细胞凋亡的潜在因素之一。这项研究旨在调查Te(TP)水醇提取物对I / R诱导的离体大鼠心脏细胞凋亡的影响。方法:将离体大鼠心脏分为六组。对照样品用Krebs-Henseleit碳酸氢盐(KHB)缓冲液灌注80分钟;在对照缺血组中,初次灌注(20分钟)后,心脏暴露于整体缺血(20分钟)和再灌注(40分钟)。预处理组分别灌注$ 500 {MuM $}的维生素C和各种TP浓度(0.5、1、2 mg / ml)20分钟,然后将心脏暴露于局部缺血再灌注20分钟和40分钟,分别。心脏动力学参数包括心率压积(RPP),心率(HR),左心室压力的最大上/下率($ { pm} dp / dt $),左心室发育压力(LVDP)和冠状动脉血流(CF)是从Lab Chart软件数据获得的。在心脏样品中测量了Bax和BCl-2基因的表达。结果:用TP提取物和vit C治疗的心脏代表了心脏收缩功能和CF的有意义的改善。在预处理的TP提取物和vit C心脏中观察到Bcl-2的过表达,Bax的下调和凋亡指数(Bax / Bcl-2)的改善。结论:TP提取物可改善再灌注心肌的心功能。同样,它可以阻碍引起心脏保护的凋亡途径。

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