Determination of 18F-fluoro-2-deoxy- d-glucose rate constants in the anesthetized baboon brain with dynamic positron tomography

We have determined the rate constants (k i ∗) of 18F-fluorodeoxyglucose (FDG) in the unlesioned baboon brain, for use in positron emission tomography (PET) measurements of glucose utilization. In contrast to earlier reports, we used a radiosynthesis which garantees production of FDG essentially uncontaminated by fluorodeoxymannose, and an improved determination of k i ∗ by (1) direct measurement of the time-shift between bolus arrival in femoral arterial plasma and brain, (2) rapid initial PET frames, and (3) extended data acquisition (up to 180 min). Young adult baboons were studied under anesthesia with either phencyclidine or etomidate. The FDG time-activity curves obtained from temporal grey matter showed a consistent decline after about 80 min, indicating true product loss. Three-compartment modelling was performed for increasing fitting intervals (20–120 min) with both a 5-parameter ( K 1 ∗ − k 4 ∗ , and vascular volume ( V o)) and a 4-parameter ( K 1 ∗ − k 3 ∗, V o ) model. With the latter, both the calculated FDG net clearance ((K ∗ = K 1 ∗ · k 3 ∗/(k 2 ∗ + k 3 ∗)) and the fitted kinetic constants were dependent on fitting interval, i.e., they showed sustained unstability. With the former, the constant k 4 ∗ , which presumably represents dephosphorylation, was overestimated and unstable for short fitting times (presumably due to heterogeneous brain compartments in the sample tissue), but stabilized at − 0.01 min −1 for fitting times ≥80 min; K 1 ∗ − k 3 ∗ and K ∗ were also stable after this time. These findings were identical for both anesthetic regimen. Thus, in the anesthetized baboon, the FDG k 1 ∗ values can be reliably determined based on an adequate PET acquisition paradigm and with a model that incorporates k 4 ∗ and ≥80 min time-activity data.