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A Translational Study of a New Therapeutic Approach for Acute Myocardial Infarction: Nanoparticle-Mediated Delivery of Pitavastatin into Reperfused Myocardium Reduces Ischemia-Reperfusion Injury in a Preclinical Porcine Model

机译:急性心肌梗死的新治疗方法的转化研究:在临床前猪模型中纳米颗粒介导的匹伐他汀向再灌注心肌的递送减少了缺血-再灌注损伤。

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摘要

BackgroundThere is an unmet need to develop an innovative cardioprotective modality for acute myocardial infarction, for which interventional reperfusion therapy is hampered by ischemia-reperfusion (IR) injury. We recently reported that bioabsorbable poly(lactic acid/glycolic acid) (PLGA) nanoparticle-mediated treatment with pitavastatin (pitavastatin-NP) exerts a cardioprotective effect in a rat IR injury model by activating the PI3K-Akt pathway and inhibiting inflammation. To obtain preclinical proof-of-concept evidence, in this study, we examined the effect of pitavastatin-NP on myocardial IR injury in conscious and anesthetized pig models.
机译:背景技术迫切需要开发一种用于急性心肌梗塞的创新性心脏保护方法,该方法的介入性再灌注治疗会受到缺血再灌注(IR)损伤的阻碍。我们最近报道,用匹伐他汀(pitavastatin-NP)可生物吸收的聚乳酸/乙醇酸(PLGA)纳米粒子介导的治疗通过激活PI3K-Akt途径并抑制炎症在大鼠IR损伤模型中发挥了心脏保护作用。为了获得临床前的概念证据,在这项研究中,我们检查了匹伐他汀-NP对清醒和麻醉猪模型心肌IR损伤的影响。

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