HIGH-FREQUENCY VIBRATORY SENSITIVE NEURONS IN MONKEY PRIMARY SOMATOSENSORY CORTEX - ENTRAINED AND NONENTRAINED RESPONSES TO VIBRATION DURING THE PERFORMANCE OF VIBRATORY-CUED HAND MOVEMENTS
Ma. Lebedev et Rj. Nelson, HIGH-FREQUENCY VIBRATORY SENSITIVE NEURONS IN MONKEY PRIMARY SOMATOSENSORY CORTEX - ENTRAINED AND NONENTRAINED RESPONSES TO VIBRATION DURING THE PERFORMANCE OF VIBRATORY-CUED HAND MOVEMENTS, Experimental Brain Research, 111(3), 1996, pp. 313-325
The activity of high-frequency vibratory sensitive (HFVS) neurons was
recorded in monkey primary somatosensory cortex (SI) while animals per
formed wrist flexions and extensions in response to 57-Hz or 127-Hz pa
lmar vibration. HFVS neurons were distinguished by their exquisite res
ponsiveness to the higher frequency vibration (127 Hz). These neurons
probably received input from Pacinian afferents. Systematic selection
of HFVS neurons was made using K-means cluster analysis of neuronal fi
ring rates during stimulating at 127 Hz and 57 Hz. HFVS neurons consti
tuted similar to 4% of all recorded cells and more frequently were fou
nd in areas 3b, 1, and 2 (similar to 5% of total in each area) than in
area 3a (similar to 1%). Using circular-statistics analyses for nonun
iformity of discharges over the vibratory cycle, HFVS neurons were spl
it into two groups of vibration-entrained neurons (E1 and E2 neurons)
and one group of nonentrained neurons (NE neurons). E1 neurons were en
trained to vibration at both 127 Hz and 57 Hz, whereas E2 neurons were
entrained only at one of these vibratory frequencies. Vibration-entra
ined neurons often exhibited multimodal distributions of interspike in
tervals (ISIs), with the modes at multiples of the period of vibration
. In addition, for these neurons, ISI clusters in joint interval plots
commonly had diagonal orientations that were indicative of negative s
erial correlations of the ISIs, a feature of extrinsically driven rhyt
hmic activity. HFVS neurons located in areas 3a, 3b, and 1 responded t
o vibration onset at shorter latencies (16.5+/-1.6, 19.8+/-5.9, and 21
.4+/-6.4 ms, respectively, during 127-Hz stimulation) than those locat
ed in area 2 (35.6+/-13.8 ms). These observations are consistent with
a scheme in which HFVS area 2 neurons receive their inputs from more a
nterior areas of SI. Moreover, entrained neurons exhibited shorter res
ponse latencies than nonentrained neurons. During 127-Hz stimulation,
response latencies were 17.3+/-3.0, 17.5+/-2.6, and 25.7+/-6.4 ms for
E1, E2, and NE neurons, respectively, located in areas 3a, 3b, and 1.
Thus, entrained and nonentrained HFVS neurons may belong to different
hierarchical stages of information processing.