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首页> 外文期刊>Canadian Journal of Physiology and Pharmacology >Salvia miltiorrhiza treatment during early reperfusion reduced postischemic myocardial injury in the rat.
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Salvia miltiorrhiza treatment during early reperfusion reduced postischemic myocardial injury in the rat.

机译:早期再灌注期间丹参的治疗减少了大鼠的缺血性心肌损伤。

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Oxidative stress may play a causative role in myocardial ischemia-reperfusion injury. However, it is a relatively understudied aspect regarding an optimal timing of antioxidant intervention during ischemia-reperfusion. The present study investigates the effect of different treatment regimens of Salvia miltiorrhiza (SM) herb extracts containing phenolic compounds that possess potent antioxidant properties on postischemic myocardial functional recovery in the setting of global myocardial ischemia and reperfusion. Langendorff-perfused rat hearts were subjected to 40 min of global ischemia at 37 degrees C followed by 60 min of reperfusion, and were randomly assigned into the untreated control and 2 SM-treated groups (n = 7 per group). In treatment 1 (SM1), 3 mg/mL of water soluble extract of SM was given for 10 min before ischemia and continued during ischemia through the aorta at a reduced flow rate of 60 microL/min, but not during reperfusion. In treatment 2 (SM2), SM (3 mg/mL) was given during the first15 min of reperfusion. During ischemia, hearts in the control and SM2 groups were given physiological saline at 60 microL/min. The SM1 treatment reduced the production of 15-F2t-isoprostane, a specific index of oxidative stress-induced lipid peroxidation, during ischemia (94 +/- 20, 43 +/- 6, and 95 +/- 15 pg/mL in the coronary effluent in control, SM1, and SM2 groups, respectively; p < 0.05, SM1 vs. control or SM2) and postponed the onset of ischemic contracture. However, SM2, but not the SM1 regimen, significantly reduced 15-F2t-isoprostane production during early reperfusion and led to optimal postischemic myocardial functional recovery (left ventricular developed pressure 51 +/- 4, 46 +/- 4, and 60 +/- 6 mmHg in the control, SM1, and SM2 groups, respectively, at 60 min of reperfusion; p < 0.05, SM2 vs. control or SM1) and reduced myocardial infarct size as measured by triphenyltetrazolium chloride staining (26% +/- 2%, 22% +/- 2%, and 20% +/- 2% of the total area in the control, SM1, and SM2 groups, respectively, p < 0.05, SM2 vs. control). It is concluded that S. miltiorrhiza could be beneficial in the treatment of myocardial ischemic injury and the timing of administration seems important.
机译:氧化应激可能在心肌缺血-再灌注损伤中起一定作用。然而,关于缺血再灌注过程中抗氧化剂干预的最佳时机,这是一个相对未被充分研究的方面。本研究调查了丹参药材提取物的不同治疗方案,其中所述酚提取物具有有效的抗氧化特性,在全局性心肌缺血和再灌注情况下对缺血后心肌功能恢复具有影响。在37摄氏度下,对Langendorff灌注的大鼠心脏进行40分钟的整体缺血,然后再灌注60分钟,并随机分为未治疗的对照组和2个SM治疗组(每组n = 7)。在处理1(SM1)中,在缺血前10分钟给予3 mg / mL的SM水溶性提取物,并在缺血期间通过主动脉以60 microL / min的降低流速继续给药,但在再灌注期间不给予。在治疗2(SM2)中,在再灌注的前15分钟内给予了SM(3 mg / mL)。缺血期间,对照组和SM2组的心脏以60微升/分钟的速度给予生理盐水。 SM1处理减少了局部缺血期间15-F2t-异前列腺素的生成,这是氧化应激诱导的脂质过氧化的特定指数(在肝脏中94 +/- 20、43 +/- 6和95 +/- 15 pg / mL)。对照组,SM1和SM2组的冠状流出物; p <0.05,SM1 vs.对照组或SM2),并推迟了缺血性挛缩的发作。但是,SM2而非SM1方案可显着降低早期再灌注期间的15-F2t-异前列腺素生成,并导致最佳的缺血后心肌功能恢复(左心室发育压力51 +/- 4、46 +/- 4和60 + / -对照组,SM1和SM2组在再灌注60分钟时分别为6 mmHg; p <0.05,SM2与对照组或SM1相比),并且通过三苯基氯化四氮唑蓝染色(26%+/- 2分别为对照组,SM1和SM2组的总面积的%,22%+/- 2%和20%+/- 2%,p <0.05,SM2与对照组相比)。结论是,S。miltiorrhiza可能有益于心肌缺血性损伤的治疗,给药时间似乎很重要。

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