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. Author manuscript; available in PMC: 2017 Feb 1.
Published in final edited form as: Neurochem Int. 2015 Dec 23;93:26–39. doi: 10.1016/j.neuint.2015.12.008

Figure 5.

Figure 5

Progressive changes to the theoretical fractional [13C] abundance in the hexose phosphate and malate pools as the isotope equilibrates.

The data from Table 3 were used in the model to optimize the flux ratios (see Table 5). The model considered seven rounds of hexose phosphate recycling from the non-oxidative PPP back through the HxP pool and the oxidative PPP, with the labeling pattern after the 7th recycle used for the final calculations (Table 1). A–D shows how the fractional [13C]HxP ( FMHxP,FM1HxP,FM2HxP,FM3HxP) changes when additional rounds of recycling occur. The model also considered how [13C] in mitochondrial malate varied over 4 turns of the TCA cycle as [13C]oxaloacetate from the previous turn reacts with [13C]acetyl CoA derived from labeled pyruvate. E–H illustrates how the fractional malate labeling pattern ( FMMal,FM1Mal,FM2Mal,FM3Mal,FM4Mal) varies over each turn of the TCA cycle.