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全身和肌肉水平下13C标记底物氧化的校正因子。

Correction factors for 13C-labelled substrate oxidation at whole-body and muscle level.

作者信息

van Hall G

机构信息

The Copenhagen Muscle Research Centre, Rigshospitalet, Denmark.

出版信息

Proc Nutr Soc. 1999 Nov;58(4):979-86. doi: 10.1017/s0029665199001299.

Abstract

The oxidation of fatty acids, carbohydrates and amino acids can be measured by quantifying the rate of excretion of labelled CO2 following administration of 14C- or 13C-labelled substrates at whole-body and tissue level. However, there is a theoretical need to correct the oxidation rates for the proportion of labelled CO2 that is produced via oxidation but not excreted. Furthermore, depending on the substrate and position of the C label(s), there may also be a need to correct for labelled C from the metabolized substrate that does not appear as CO2, but rather becomes temporarily fixed in other metabolites. The bicarbonate correction factor is used to correct for the labelled CO2 not excreted. Recently, an acetate correction factor has been proposed for the simultaneous correction of CO2 not excreted and label fixed in other metabolites via isotopic exchange reactions, mainly in the tricarboxylic acid cycle. Changes in metabolic rate induced, for example, by feeding, hormonal changes and physical activity, as well as infusion time, have been shown to affect both correction factors. The present paper explains the theoretical and physiological basis of these correction factors and makes recommendations as to how these correction factors should be used in various physiological conditions.

摘要

脂肪酸、碳水化合物和氨基酸的氧化作用可通过在全身和组织水平给予¹⁴C或¹³C标记的底物后,对标记二氧化碳的排泄率进行定量来测定。然而,理论上需要对氧化率进行校正,以考虑通过氧化产生但未排泄的标记二氧化碳的比例。此外,根据底物和碳标记的位置,可能还需要对代谢底物中未以二氧化碳形式出现、而是暂时固定在其他代谢产物中的标记碳进行校正。碳酸氢盐校正因子用于校正未排泄的标记二氧化碳。最近,有人提出了一种乙酸盐校正因子,用于同时校正未排泄的二氧化碳以及通过同位素交换反应(主要发生在三羧酸循环中)固定在其他代谢产物中的标记物。已证明,例如由进食、激素变化和身体活动引起的代谢率变化以及输注时间,都会影响这两种校正因子。本文解释了这些校正因子的理论和生理基础,并就如何在各种生理条件下使用这些校正因子提出了建议。

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