The primary motor cortex and supplementary motor area (SMA) are purpor
tedly involved in the generation of the P22 and N30 components of soma
tosensory evoked potentials (SEPs) evoked by electrical stimulation of
the median nerve at the wrist. We used regional cerebral blood flow (
rCBF) measurements and PET in 10 normal subjects to study the cerebral
areas activated by median nerve electrical stimulation. PET scans wer
e performed with the subjects at rest and during stimulation of the ri
ght median nerve at frequencies of up to 20 Hz. Stimulation evoked a s
ingle focus of activation in the primary somatosensory area (SI). An i
ncrease of rCBF in this area was linearly correlated with stimulus fre
quencies of up to 4 Hz and then reached a plateau. The SMA was not sig
nificantly activated by stimulation at arty of the frequencies tested.
In contrast to the SI, the SMA showed no trend toward a correlation b
etween the rCBF changes and the stimulus repetition rate. In order to
achieve maximal resolution in the sensorimotor cortex, regions of inte
rest were placed in individual co-registered MRI-PET images on both si
des of the central sulcus. There was no significant increase of rCBF i
n the crown of the precentral gyrus. These results suggest that a cont
ribution of the primary motor cortex and the SMA to the generation of
the P22 and N30 components of SEPs is unlikely. Consequently, function
al clinical interpretations derived from P22 or N30 abnormalities must
be reconsidered.