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. Author manuscript; available in PMC: 2010 Jan 1.
Published in final edited form as: J Cereb Blood Flow Metab. 2008 Sep 3;29(1):108–118. doi: 10.1038/jcbfm.2008.102

Table 2.

Standard deviation of the glutamate–glutamine cycling flux determined using Monte Carlo analysis when astrocytic dilution is omitted from the two-compartment modela,b

Constraints (μmol/g/min) Mean Vcyc (μmol/g/min) Relative s.d. Vcycc(%) Noise level (μmol/g)
None 0.50 438 0.2
0.27 66 0.1
aVTCA≤0.1, Vefflux = 0.2VGln 0.27 32 0.2
0.26 21 0.1

VTCA, tricarboxylic acid cycle flux; Vefflux, rate of glutamine efflux; VGln, flux of glutamine synthesis.

a

All simulations were carried out with a total infusion time of 160 mins and temporal resolution of 5 mins (32 time points). Only the glutamate C4 and glutamine C4 turnover curves were used for extraction of the metabolic fluxes. When Vdil(Gln) is forced to zero 13C-labeled glutamine concentration predicted by the model is higher than that shown in Figure 2A. The 13C-labeled glutamine concentration with Vdil(Gln) = 0 was made to match that in Figure 2A by reducing the total glutamine concentration to 2.8 mmol/L in the Monte Carlo simulations. This was done in order to simulate the Gruetter et al (2001) model (Shestov et al, 2007) where astroglial dilution was omitted.

b

Mean χ2 of all simulations lies in the range of 60.2–61.1 with a standard deviation in the range of 10.9–11.3.

c

With respect to the nominal Vcyc = 0.32 μmol/g/min.