(13)二维核磁共振C葡萄糖标记研究是测定肾脏低温机器灌注过程中体外全器官代谢的有用工具。

Transplantation research Pub Date : 2016-08-05 eCollection Date: 2016-01-01 DOI:10.1186/s13737-016-0037-0
Jay Nath, Tom Smith, Alex Hollis, Sam Ebbs, Sefa W Canbilen, Daniel A Tennant, Andrew R Ready, Christian Ludwig
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引用次数: 17

摘要

背景:本研究的目的是确定使用核磁共振(NMR)示踪剂研究((13)富含c的葡萄糖)来检测低温机器灌注(HMP)期间猪肾脏灌注液和皮质组织中的体外新生代谢的可行性。方法:采用器官恢复系统LifePort肾灌注装置对6个猪肾进行24 h HMP灌注。葡萄糖用稳定同位素(13)C ([U-(13)C]葡萄糖)均匀富集,以10 mM浓度加入kps -1样灌注液中。灌注液采用1D (1)H和2D (1)H,(13)C异核单量子相干(HSQC) NMR波谱分析。然后通过量化灌注液和组织样品中含有(13)C的关键代谢物的比例来研究代谢活性。结果:在灌注液和组织提取物中存在的许多中心代谢物中都有(13)C的显著富集,其中乳酸和丙氨酸最为明显。在HMP过程中,灌注液中乳酸的总量(每个样品)增加(6h时为31.1±12.2 nmol, 24h时为93.4±25.6 nmol)。结论:本研究最终证明了HMP过程中发生了新生代谢,并突出了在这种低温、缺氧环境下活跃的代谢途径。虽然大多数(13)c富集的葡萄糖被代谢成糖酵解终点代谢物,如乳酸,但非糖酵解途径衍生物的存在表明,HMP过程中的代谢比以前认为的要复杂得多。同位素标记体外器官灌注研究使用二维核磁共振是可行的和翔实的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

(13)C glucose labelling studies using 2D NMR are a useful tool for determining ex vivo whole organ metabolism during hypothermic machine perfusion of kidneys.

(13)C glucose labelling studies using 2D NMR are a useful tool for determining ex vivo whole organ metabolism during hypothermic machine perfusion of kidneys.

(13)C glucose labelling studies using 2D NMR are a useful tool for determining ex vivo whole organ metabolism during hypothermic machine perfusion of kidneys.

(13)C glucose labelling studies using 2D NMR are a useful tool for determining ex vivo whole organ metabolism during hypothermic machine perfusion of kidneys.

Background: The aim of this study is to determine the feasibility of using nuclear magnetic resonance (NMR) tracer studies ((13)C-enriched glucose) to detect ex vivo de novo metabolism in the perfusion fluid and cortical tissue of porcine kidneys during hypothermic machine perfusion (HMP).

Methods: Porcine kidneys (n = 6) were subjected to 24 h of HMP using the Organ Recovery Systems LifePort Kidney perfusion device. Glucose, uniformly enriched with the stable isotope (13)C ([U-(13)C] glucose), was incorporated into KPS-1-like perfusion fluid at a concentration of 10 mM. Analysis of perfusate was performed using both 1D (1)H and 2D (1)H,(13)C heteronuclear single quantum coherence (HSQC) NMR spectroscopy. The metabolic activity was then studied by quantifying the proportion of key metabolites containing (13)C in both perfusate and tissue samples.

Results: There was significant enrichment of (13)C in a number of central metabolites present in both the perfusate and tissue extracts and was most pronounced for lactate and alanine. The total amount of enriched lactate (per sample) in perfusion fluid increased during HMP (31.1 ± 12.2 nmol at 6 h vs 93.4 ± 25.6 nmol at 24 h p < 0.01). The total amount of enriched alanine increased in a similar fashion (1.73 ± 0.89 nmol at 6 h vs 6.80 ± 2.56 nmol at 24 h p < 0.05). In addition, small amounts of enriched acetate and glutamic acid were evident in some samples.

Conclusions: This study conclusively demonstrates that de novo metabolism occurs during HMP and highlights active metabolic pathways in this hypothermic, hypoxic environment. Whilst the majority of the (13)C-enriched glucose is metabolised into glycolytic endpoint metabolites such as lactate, the presence of non-glycolytic pathway derivatives suggests that metabolism during HMP is more complex than previously thought. Isotopic labelled ex vivo organ perfusion studies using 2D NMR are feasible and informative.

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