首页> 外文期刊>Molecular and Cellular Biochemistry: An International Journal for Chemical Biology >Effects of pharmacological preconditioning by emodin/oleanolic acid treatment and/or ischemic preconditioning on mitochondrial antioxidant components as well as the susceptibility to ischemia-reperfusion injury in rat hearts
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Effects of pharmacological preconditioning by emodin/oleanolic acid treatment and/or ischemic preconditioning on mitochondrial antioxidant components as well as the susceptibility to ischemia-reperfusion injury in rat hearts

机译:大黄素/油酸处理和/或缺血预处理对药理预处理对大鼠心脏线粒体抗氧化剂成分及缺血再灌注敏感性的影响

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摘要

Using an ex vivo rat heart model of ischemia-reperfusion (I-R) injury, we examined the effect of pharmacological preconditioning by chronic treatment with emodin (EMD)/oleanolic acid (OA) at low dose (25 mu mol/kg/day x 15) and/or ischemic preconditioning (IPC) (4 cycles of 5 min ischemia followed by 5 min of reperfusion) on myocardial I-R injury. The results indicated that EMD/OA pretreatment, IPC, or their combinations (EMD+IPC and OA+IPC) protected against myocardial I-R injury, as assessed by lactate dehydrogenase leakage and contractile force recovery. The cardioprotection was associated with a differential enhancement in mitochondrial antioxidant components. The combined EMD/OA and IPC pretreatment produced cardioprotective action in a semi-additive manner. This suggested that EMD/OA pretreatment and IPC protected against myocardial I-R injury via a similar but not identical biochemical mechanism.
机译:使用离体大鼠缺血再灌注(IR)损伤的心脏模型,我们通过大剂量低剂量(25μmol / kg /天x大黄素(EMD)/油酸(OA)的慢性治疗,研究了药理学预处理的效果)和/或缺血性预处理(IPC)(4个周期,即5分钟局部缺血,再进行5分钟再灌注)治疗心肌IR损伤。结果表明,通过乳酸脱氢酶渗漏和收缩力恢复评估,EMD / OA预处理,IPC或它们的组合(EMD + IPC和OA + IPC)可以防止心肌I-R损伤。心脏保护作用与线粒体抗氧化剂成分的差异性增强有关。 EMD / OA和IPC预处理相结合以半加成方式产生了心脏保护作用。这表明EMD / OA预处理和IPC通过类似但不完全相同的生化机制来保护心肌免受I-R损伤。

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