We determined regional incorporation coefficients (k) of plasma [1-C-
11]palmitate into stable brain lipids of anesthetized monkeys with PET
. Methods: Carbon-11-palmitate was injected intravenously in untreated
animals and in animals pretreated with methyl palmoxirate (MEP), an i
nhibitor of beta-oxidation of palmitate in the brain and periphery. Pl
asma radioactivity was followed, and brain radioactivity was determine
d at various times using PET. A least-squares method was used to fit t
he data to an operational equation to obtain regional values of k and
of cerebral blood volume (V-b) in individual experiments. Results: ME
P significantly decreased the integral of plasma [C-11]CO2 following C
-11-paalmtate infusion. Mean values of k in monkeys not given MEP wer
e 4.9, 4.2, 4.9, 4.0 and 2.9 x 10(-5) ml/sec g for the temporal, front
al, parietal and occipital cortices and white matter, respectively. Wi
th the exception of k in white matter, which was increased by MEP, k*
in the other brain regions was not significantly changed by MEP. The
V-b ranged from 0.035 ml/g to 0.048 ml/g in gray matter regions and eq
ualed 0.022 ml/g in white matter. Conclusion: PET can be used to deter
mine regional incorporation coefficients of C-11-palmitate into the pr
imate brain in vivo. Combined with MEP, C-11-palmitate could be used w
ith PET to examine regional brain phospholipid metabolism in humans in
normal and pathological conditions.