Radioactive tracer substances administered to study cerebral functions
open a time-dependent window to the brain. We can study e.g. regional
cerebral blood flow (rCBF) or chemical properties such as receptors f
or transmitter substances. Since the tracer substance is carried by th
e blood flow into the brain its initial distribution will be proportio
nal to the rCBF. The possibility to study more specific brain function
s depends on the available time for redistribution of the tracer subst
ance according to its specific chemical affinity. I have studied with
the aid of a simple mathematic model the time needed for distribution
and redistribution of freely diffusable tracer substances in the brain
. The results indicate that SPECT measurements of brain receptor prope
rties in theory give at least as good recording conditions as correspo
nding PET studies. Clinical SPECT receptor studies will presumably soo
n contribute to our knowledge of the epileptic pathogenic mechanisms.