首页> 外文期刊>Frontiers in Surgery >Pharmacological Activating Transcription Factor 6 Activation Is Beneficial for Liver Retrieval With ex vivo Normothermic Mechanical Perfusion From Cardiac Dead Donor Rats
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Pharmacological Activating Transcription Factor 6 Activation Is Beneficial for Liver Retrieval With ex vivo Normothermic Mechanical Perfusion From Cardiac Dead Donor Rats

机译:药理活化转录因子6激活是有益于肝脏检索来自心脏死亡者大鼠的eMVivo常温机械灌注

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Background: Normothermic machine perfusion (NMP) could be beneficial for organ retrieval from donors after cardiac death (DCD). Activating transcription factor 6 (ATF6) was recently shown to mitigate liver ischemia/reperfusion injury and confer protection. The aims of this study were to assess the implication of ATF6 in liver retrieval from DCD rat livers with NMP and explore the effect of pharmacologic ATF-6 activation on liver retrieval. Methods: The livers from DCD rats were exposed to 30 min of warm ischemia and 8 h cold preservation followed by 2 h NMP with or without an ATF6 activator in the perfusate. Perfusates and livers were harvested to detect ATF6 expression, liver function, and inflammation. Results: DCD livers with NMP were associated with ATF6 overexpression and activation based on IHC and WB ( P 0.05). The ATF6 activator downregulated perfusate aminotransferases, decreased the Suzuki score, downregulated CD68 and MPO based on IHC, induced the expression of cytochrome c in mitochondria and inhibited the expression of cytochrome c in cytoplasm based on WB, reduced TNFα and IL-6 levels based on ELISA, decreased levels of MDA, GSSG and ATP, and increased SOD activity and GSH levels in the perfused livers ( P 0.05). Conclusion: ATF6 is important for liver retrieval, and an exogenous ATF6 activator accelerates liver retrieval from DCD rats in an ex vivo NMP model.
机译:背景:常温机灌注(NMP)可能有利于心脏死亡(DCD)后供体的器官检索。最近显示激活转录因子6(ATF6)以减轻肝脏缺血/再灌注损伤和赋予保护。本研究的目的是评估ATF6在具有NMP的DCD大鼠肝脏肝脏检索中的含义,并探讨药理学ATF-6活化对肝脏检索的影响。方法:从DCD大鼠的肝脏暴露于30分钟的温暖缺血和8小时冷保,然后在灌注液中有2小时,或没有ATF6活化剂。收获灌注物和肝脏以检测ATF6表达,肝功能和炎症。结果:具有NMP的DCD肝脏与ATF6过表达和基于IHC和WB的激活相关联(P <0.05)。 ATF6活化剂下调灌注氨酸氨基转移酶,下调基于IHC的铃木评分,下调的CD68和MPO,诱导细胞色素C在线粒体中的表达,并抑制基于WB的细胞质中细胞色素C的表达,降低TNFα和IL-6水平。 ELISA,MDA,GSSG和ATP水平降低,以及灌注肝脏中的SOD活性和GSH水平增加(P <0.05)。结论:ATF6对于肝脏检索至关重要,外源ATF6激活剂从EXVivo NMP模型中的DCD大鼠加速肝脏检索。

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