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用于校正人体中[U-13C]棕榈酸氧化率的[1,2-13C]乙酸回收因子的验证。

Validation of the [1,2-13C]acetate recovery factor for correction of [U-13C]palmitate oxidation rates in humans.

作者信息

Schrauwen P, van Aggel-Leijssen D P, van Marken Lichtenbelt W D, van Baak M A, Gijsen A P, Wagenmakers A J

机构信息

Department of Human Biology, Maastricht University, The Netherlands.

出版信息

J Physiol. 1998 Nov 15;513 ( Pt 1)(Pt 1):215-23. doi: 10.1111/j.1469-7793.1998.215by.x.

Abstract
  1. The validity of estimations of plasma fatty acid oxidation using tracers has often been questioned. The appearance of isotopic markers in breath CO2 is delayed and incomplete. Recently suggestions have been made that substantial amounts of tracer are incorporated into products of the tricarboxylic acid cycle (e.g. glucose, glutamine and glutamate) and that an acetate correction factor can be used to correct for tracer fixation. In the present study we investigated whether the appearance of 13CO2 during a separate infusion of [1,2-13C]acetate could be used for correction of [U-13C]palmitate oxidation rates in studies lasting <2 h and we quantified the appearance of tracer in the glutamine, glutamate and glucose pools of the body. 2. An infusion of either [1,2-13C]acetate (0.104 micromol min-1 kg-1) or [U-13C]palmitate (0.013 micromol min-1 kg-1) was given to eight male subjects and continued for 2 h at rest. In six subjects the infusion of [1,2-13C]acetate was repeated to determine reproducibility of the acetate recovery. 3. Fractional recovery in breath from [1,2-13C]acetate gradually increased during the infusion period at rest from 14.1 +/- 0.6% at 60 min to 26.5 +/- 0.5% at 120 min after the start of the infusion. Intersubject coefficient of variance was 8.3 +/- 0.6% and intrasubject coefficient of variance of the acetate recovery tests was 4.0 +/- 1.5%. After 2 h of [1,2-13C]acetate infusion, 12.4 +/- 0.8 and 10.3 +/- 0.9% of infused 13C was incorporated in the glutamine and glutamate pools, respectively. 4. In conclusion, the [1,2-13C]acetate recovery factor can be used for correcting the rate of [U-13C]palmitate oxidation in infusing studies of 2 h in resting conditions. Failure to use this recovery factor leads to a substantial underestimation of the rate of plasma free fatty acid oxidation. The extent of label fixation could largely be explained by accumulation of tracer carbon in glutamine and glutamate, and the accumulation in glucose is negligible.
摘要
  1. 使用示踪剂估算血浆脂肪酸氧化的有效性常常受到质疑。呼吸二氧化碳中同位素标记物的出现延迟且不完全。最近有人提出,大量示踪剂会掺入三羧酸循环的产物(如葡萄糖、谷氨酰胺和谷氨酸)中,并且可以使用乙酸校正因子来校正示踪剂的固定。在本研究中,我们调查了在单独输注[1,2-¹³C]乙酸期间¹³CO₂的出现是否可用于校正持续时间小于2小时的研究中[U-¹³C]棕榈酸的氧化速率,并且我们对示踪剂在人体谷氨酰胺、谷氨酸和葡萄糖池中的出现进行了定量。2. 给八名男性受试者输注[1,2-¹³C]乙酸(0.104微摩尔·分钟⁻¹·千克⁻¹)或[U-¹³C]棕榈酸(0.013微摩尔·分钟⁻¹·千克⁻¹),并在静息状态下持续2小时。在六名受试者中重复输注[1,2-¹³C]乙酸以确定乙酸回收率的可重复性。3. 在静息状态下的输注期间,[1,2-¹³C]乙酸在呼吸中的分数回收率从输注开始后60分钟时的14.1±0.6%逐渐增加到120分钟时的26.5±0.5%。受试者间变异系数为8.3±0.6%,乙酸回收率测试的受试者内变异系数为4.0±1.5%。在输注[1,2-¹³C]乙酸2小时后,分别有12.4±0.8%和10.3±0.9%的输注¹³C掺入谷氨酰胺和谷氨酸池中。4. 总之,[1,2-¹³C]乙酸回收率因子可用于校正静息状态下2小时输注研究中[U-¹³C]棕榈酸的氧化速率。未使用该回收率因子会导致血浆游离脂肪酸氧化速率被大幅低估。标记固定的程度在很大程度上可以由示踪剂碳在谷氨酰胺和谷氨酸中的积累来解释,而在葡萄糖中的积累可以忽略不计。

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