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Organ-specific responses during brain death: increased aerobic metabolism in the liver and anaerobic metabolism with decreased perfusion in the kidneys

机译:脑死亡期间的器官特异性反应:肝脏中有氧代谢增加和厌氧代谢,肾脏灌注减少

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Hepatic and renal energy status prior to transplantation correlates with graft survival. However, effects of brain death (BD) on organ-specific energy status are largely unknown. We studied metabolism, perfusion, oxygen consumption, and mitochondrial function in the liver and kidneys following BD. BD was induced in mechanically-ventilated rats, inflating an epidurally-placed Fogarty-catheter, with sham-operated rats as controls. A 9.4T-preclinical MRI system measured hourly oxygen availability (BOLD-related R2*) and perfusion (T1-weighted). After 4 hrs, tissue was collected, mitochondria isolated and assessed with high-resolution respirometry. Quantitative proteomics, qPCR, and biochemistry was performed on stored tissue/plasma. Following BD, the liver increased glycolytic gene expression (Pfk-1) with decreased glycogen stores, while the kidneys increased anaerobic- (Ldha) and decreased gluconeogenic-related gene expression (Pck-1). Hepatic oxygen consumption increased, while renal perfusion decreased. ATP levels dropped in both organs while mitochondrial respiration and complex I/ATP synthase activity were unaffected. In conclusion, the liver responds to increased metabolic demands during BD, enhancing aerobic metabolism with functional mitochondria. The kidneys shift towards anaerobic energy production while renal perfusion decreases. Our findings highlight the need for an organ-specific approach to assess and optimise graft quality prior to transplantation, to optimise hepatic metabolic conditions and improve renal perfusion while supporting cellular detoxification.
机译:移植前的肝和肾能量状态与移植物存活相关。但是,脑死亡(BD)对器官特异性能量状态的影响在很大程度上尚不清楚。我们研究了BD后肝脏和肾脏的新陈代谢,灌注,耗氧量和线粒体功能。在机械通气的大鼠中诱发BD,以假手术大鼠作为对照,使硬膜外置入的Fogarty导管膨胀。一个9.4T的临床前MRI系统测量每小时的氧气供应量(与BOLD相关的R2 *)和灌注(T1加权)。 4小时后,收集组织,分离线粒体并用高分辨率呼​​吸测定法评估。对储存的组织/血浆进行了蛋白质组学,定量PCR和生物化学定量分析。 BD后,肝脏增加了糖酵解基因表达(Pfk-1),糖原储备减少,而肾脏则增加了厌氧(Ldha)和糖异生相关基因表达(Pck-1)。肝耗氧量增加,而肾灌注减少。 ATP水平在两个器官中均下降,而线粒体呼吸和复杂的I / ATP合酶活性未受影响。总之,肝脏对BD期间代谢需求增加有反应,并通过功能性线粒体增强有氧代谢。肾脏向无氧能量生产转移,而肾脏灌注减少。我们的发现突出表明,需要一种器官特异性方法来评估和优化移植前的移植质量,以优化肝脏代谢状况并改善肾脏灌注,同时支持细胞排毒。

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