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Metabolomic and Mass Isotopomer Analysis of Liver Gluconeogenesis and Citric Acid Cycle: II. HETEROGENEITY OF METABOLITE LABELING PATTERN*

机译:肝糖异生和代谢的代谢组学和质量同位素异构体分析 柠檬酸循环:II。代谢物标签的异质性 图案*

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摘要

In this second of two companion articles, we compare the mass isotopomer distribution of metabolites of liver gluconeogenesis and citric acid cycle labeled from NaH13CO3 or dimethyl [1,4-13C2]succinate. The mass isotopomer distribution of intermediates reveals the reversibility of the isocitrate dehydrogenase + aconitase reactions, even in the absence of a source of α-ketoglutarate. In addition, in many cases, a number of labeling incompatibilities were found as follows: (i) glucose versus triose phosphates and phosphoenolpyruvate; (ii) differences in the labeling ratios C-4/C-3 of glucose versus (glyceraldehyde 3-phosphate)/(dihydroxyacetone phosphate); and (iii) labeling of citric acid cycle intermediates in tissue versus effluent perfusate. Overall, our data show that gluconeogenic and citric acid cycle intermediates cannot be considered as sets of homogeneously labeled pools. This probably results from the zonation of hepatic metabolism and, in some cases, from differences in the labeling pattern of mitochondrial versus extramitochondrial metabolites. Our data have implications for the use of labeling patterns for the calculation of metabolic rates or fractional syntheses in liver, as well as for modeling liver intermediary metabolism.
机译:在这两篇配套文章的第二篇中,我们比较了NaH13CO3或[1,4-13C2]琥珀酸二甲酯标记的肝糖异生和柠檬酸循环代谢产物的质量同位素异构体分布。中间体的质量同位素异构体分布揭示了异柠檬酸脱氢酶+乌头酸酶反应的可逆性,即使在没有α-酮戊二酸源的情况下也是如此。此外,在许多情况下,发现许多标记不相容性如下:(i)葡萄糖与磷酸三糖和磷酸烯醇丙酮酸的关系; (ii)葡萄糖与(3-磷酸甘油醛)/(磷酸二羟基丙酮)的标记率C-4 / C-3的差异; (iii)组织中柠檬酸循环中间体相对于流出液的标记。总体而言,我们的数据表明,糖异生和柠檬酸循环中间体不能视为均一标记池的集合。这可能是由于肝脏代谢的区域化,在某些情况下,是由于线粒体和线粒体代谢产物的标记方式不同。我们的数据对使用标记模式来计算肝脏的代谢率或分数合成以及建模肝脏中间代谢具有重要意义。

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