Matthews D E, Cobelli C
Department of Medicine, Cornell University Medical College, New York, New York.
JPEN J Parenter Enteral Nutr. 1991 May-Jun;15(3):86S-89S. doi: 10.1177/014860719101500386S.
The metabolism of amino acids is far more complicated than a 1- to 2-pool model, yet, such simple models have been extensively used with many different isotopically labeled tracers to study protein metabolism. A tracer of leucine and measurement of leucine kinetics has been a favorite choice for following protein metabolism. However, administering a leucine tracer and following it in blood will not adequately reflect the complex, multi-pool nature of the leucine system. Using the tracer enrichment of the ketoacid metabolite of leucine, alpha-ketoisocaproate (KIC), to reflect intracellular events of leucine was an important improvement. Whether this approach is adequate to follow accurately leucine metabolism in vivo or not has not been tested. From data obtained using simultaneous administration of leucine and KIC tracers, we developed a 10-pool model of the in vivo leucine-KIC and bicarbonate kinetic system. Data from this model were compared with conventional measurements of leucine kinetics. The results from the 10-pool model agreed best with the simplified approach using a leucine tracer and measurement of KIC enrichment.
氨基酸的代谢远比单池或双池模型复杂得多,然而,这种简单模型已被广泛用于许多不同的同位素标记示踪剂来研究蛋白质代谢。亮氨酸示踪剂以及亮氨酸动力学测量一直是追踪蛋白质代谢的首选方法。然而,给予亮氨酸示踪剂并在血液中追踪它并不能充分反映亮氨酸系统复杂的多池性质。利用亮氨酸的酮酸代谢产物α-酮异己酸(KIC)的示踪剂富集来反映亮氨酸的细胞内事件是一项重要的改进。这种方法是否足以在体内准确追踪亮氨酸代谢尚未得到验证。根据同时给予亮氨酸和KIC示踪剂所获得的数据,我们建立了体内亮氨酸 - KIC和碳酸氢盐动力学系统的十池模型。将该模型的数据与亮氨酸动力学的传统测量结果进行了比较。十池模型的结果与使用亮氨酸示踪剂和KIC富集测量的简化方法最为吻合。