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Analysis of Cardioprotective Effects Using Purified Salvia miltiorrhiza Extract on Isolated Rat Hearts

机译:纯化丹参提取物对离体大鼠心脏的心脏保护作用分析

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References(14) Cited-By(25) The purpose of the current study is to evaluate the cardioprotective effects of purified Salvia miltiorrhiza extract (PSME) on myocardial ischemia/reperfusion injury in isolated rat hearts. Hearts were excised and perfused at constant flow (7 – 9 ml · min−1) via the aorta. Non-recirculating perfusion with Krebs-Henseleit (KH) solution was maintained at 37°C and continuously gassed with 95% O2 and 5% CO2. KH solution with or without PSME (100 mg per liter solution) was used after 30-min zero-flow ischemia for the PSME and control group, respectively. Left ventricular (LV) developed pressure; its derivatives, diastolic pressure, and so on were continuously recorded via a pressure transducer attached to a polyvinylchloride balloon that was placed in the left ventricle through an incision in the left atrium. PSME treated hearts showed significant postischemic contractile function recovery (developed pressure recovered to 44.2 ± 4.9% versus 17.1 ± 5.7%, P<0.05; maximum contraction recovered to 57.2 ± 5.9% versus 15.1 ± 6.3%, P<0.001; maximum relaxation restored to 69.3 ± 7.3% versus 15.4 ± 6.3%, P<0.001 in the PSME and control group, respectively). Significant elevation in end-diastolic pressure, which indicated LV stiffening in PSME hearts might have resulted from the excess high dose of PSME used. Further study will be conducted on the potential therapeutic value with lower dose of PSME on prevention of ischemic heart disease.
机译:参考文献(14)引用了(25)本研究的目的是评估纯化的丹参提取物(PSME)对离体大鼠心脏的心肌缺血/再灌注损伤的心脏保护作用。切开心脏并通过主动脉以恒定流量(7 – 9 ml·min-1)进行灌注。使用Krebs-Henseleit(KH)溶液的非循环灌流保持在37°C,并连续注入95%O2和5%CO2的气体。 PSME和对照组的零流量缺血30分钟后分别使用有或没有PSME的KH溶液(每升溶液100 mg)。左心室(LV)产生压力;它的衍生物,舒张压等通过连接到聚氯乙烯球囊的压力传感器连续记录,该球囊通过左心房的切口放置在左心室中。经PSME治疗的心脏显示出明显的缺血后收缩功能恢复(发达压力恢复至44.2±4.9%与17.1±5.7%,P <0.05;最大收缩恢复至57.2±5.9%与15.1±6.3%,P <0.001;最大松弛恢复至PSME和对照组分别为69.3±7.3%和15.4±6.3%,P <0.001)。舒张末期压力显着升高,表明PSME心脏左室僵硬可能是由于过量使用PSME引起的。进一步研究以较低剂量的PSME预防缺血性心脏病的潜在治疗价值。

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