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