Journal
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM
Volume 309, Issue 8, Pages E727-E735Publisher
AMER PHYSIOLOGICAL SOC
DOI: 10.1152/ajpendo.00216.2015
Keywords
metabolic disease; fatty liver; diabetes; insulin resistance; NASH; stable isotopes
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Two groups recently used different tracer methods to quantify liver-specific flux rates. The studies had a similar goal, i.e., to characterize mitochondrial oxidative function. These efforts could have a direct impact on our ability to understand metabolic abnormalities that affect the pathophysiology of fatty liver and allow us to examine mechanisms surrounding potential therapeutic interventions. Briefly, one method couples the continuous infusion of [C-13] acetate with direct real-time measurements of [C-13] glutamate labeling in liver; the other method administers [C-13] propionate, in combination with other tracers, and subsequently measures the C-13 labeling of plasma glucose and/or acetaminophen-glucuronide. It appears that a controversy has arisen, since the respective methods yielded different estimates of the anaplerotic/TCA flux ratio ( VANA: VTCA) in control subjects, i.e., the [C-13] acetate-and [C-13] propionatederived VANA: VTCA flux ratios appear to be similar to 1.4 and similar to 5, respectively. While the deep expertise in the respective groups makes it somewhat trivial for each to perform the tracer studies, the data interpretation is inherently difficult. The current perspective was undertaken to examine potential factors that could account for or contribute to the apparent differences. Attention was directed toward 1) matters of practicality, 2) issues surrounding stoichiometry, and 3) hidden assumptions. We believe that the [C-13] acetate method has certain weaknesses that limit its utility; in contrast, the [C-13] propionate method likely yields a more correct answer. We hope our discussion will help clarify the differences in the recent reports. Presumably this will be of interest to investigators who are considering tracer-based studies of liver metabolism.
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