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Role of NF-κB in protection of EPO pretreatment on neonatal rat cardiac myocytes with hypoxia/reoxygenation injury

机译:NF-κB在缺氧/复氧新生大鼠心肌细胞EPO预处理中的保护作用

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Objective: To observe the protective effects of erythropoietin (EPO) pretreatment on cardiac myocyte with hypoxia/reoxygenation (H/R) injury and the role of NF-κB in this effects. Methods: After the H/R model of cardiac myocytes of neonatal rats was established, the cultured cardiac myocytes were divided into 4 groups, including EPO pretreatment group ( EPO 10 U/ml 24 h before H/R), EPO pretreatment + PDTC group( EPO 10 U/ml and PDTC 5 μg/ml 24 h before H/R), PDTC group (PI)TC 5 μg/ml 24 h before H/R) and control group. Before and after the H/R, assay of LDH concentration in the culture medium, the survival rate of the myocytes tested by MTT chromatometry and the apoptosis by flow cytometry were undertaken. Activation of NF-κB was determined by EMSA before and after H/R. Results:EPO pretreatment markedly reduced the LDH concentration in the medium, elevated the survival rate of myocytes and inhibited the apoptosis after H/R. Addition of PDTC during the pretreatment abolished the protective effects of EPO pretreatment. NF-κB was markedly activated during EPO pretreatment and PDTC inhibited the activation. However, after H/R, the activity of NF-κB in myocytes with EPO pretreatment was significantly inhibited compared to the other myocytes. Conclusion: NF-κB is significantly activated during EPO pretreatment, but is inhibited after H/R, which is correlated with the protective effects of EPO pretreatment on cardiac myocytes with H/R. This phenomenon can be explained as the negative feedback mechanism of the activation of NF-κB.
机译:目的:观察促红细胞生成素(EPO)预处理对缺氧/复氧(H / R)损伤的心肌细胞的保护作用,以及NF-κB的作用。方法:建立新生大鼠心肌细胞H / R模型后,将培养的心肌细胞分为4组:EPO预处理组(H / R前24 h EPO 10 U / ml),EPO预处理+ PDTC组(EPO 10 U / ml和PDTC 5μg/ ml在H / R之前24 h),PDTC组(PI)TC在H / R 24 h之前5μg/ ml)和对照组。在H / R之前和之后,进行培养基中LDH浓度的测定,MTT色谱法检测的心肌细胞的存活率和流式细胞仪检测的细胞凋亡。 H / R前后通过EMSA测定NF-κB的活化。结果:EPO预处理可显着降低培养基中LDH的浓度,提高心肌细胞的存活率并抑制H / R后的细胞凋亡。在预处理过程中添加PDTC消除了EPO预处理的保护作用。在EPO预处理期间,NF-κB被显着激活,而PDTC抑制了该激活。然而,在H / R之后,与其他心肌细胞相比,经EPO预处理的心肌细胞中NF-κB的活性被显着抑制。结论:NF-κB在EPO预处理过程中被显着激活,但在H / R后被抑制,这与EPO预处理对H / R对心肌细胞的保护作用有关。这种现象可以解释为NF-κB活化的负反馈机制。

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