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The Journal of Neurophysiology Vol. 82 No. 1 July 1999, pp. 16-33
Copyright ©1999 by the American Physiological Society
Departments of 1Biomedical Engineering and 2Physiology, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina 27599
Tommerdahl, M.,
K. A. Delemos,
B. L. Whitsel,
O. V. Favorov, and
C. B. Metz.
Response of Anterior Parietal Cortex to Cutaneous Flutter Versus
Vibration. J. Neurophysiol. 82: 16-33, 1999.
The response of anesthetized squirrel monkey
anterior parietal (SI) cortex to 25 or 200 Hz sinusoidal vertical skin
displacement stimulation was studied using the method of optical
intrinsic signal (OIS) imaging. Twenty-five-Hertz ("flutter")
stimulation of a discrete skin site on either the hindlimb or forelimb
for 3-30 s evoked a prominent increase in absorbance
within cytoarchitectonic areas 3b and 1 in the contralateral
hemisphere. This response was confined to those area 3b/1 regions
occupied by neurons with a receptive field (RF) that includes the
stimulated skin site. In contrast, same-site 200-Hz stimulation
("vibration") for 3-30 s evoked a decrease in
absorbance in a much larger territory (most frequently involving areas
3b, 1, and area 3a, but in some subjects area 2 as well) than the
region that undergoes an increase in absorbance during 25-Hz flutter
stimulation. The increase in absorbance evoked by 25-Hz flutter
developed quickly and remained relatively constant for as long as
stimulation continued (stimulus duration never exceeded 30 s). At
1-3 s after stimulus onset, the response to 200-Hz stimulation, like
the response to 25-Hz flutter, consisted of a localized increase in
absorbance limited to the topographically appropriate region of area 3b
and/or area 1. With continuing 200-Hz stimulation, however, the early
response declined, and by 4-6 s after stimulus onset, it was replaced
by a prominent and spatially extensive decrease in absorbance. The
spike train responses of single quickly adapting (QA) neurons were
recorded extracellularly during microelectrode penetrations that
traverse the optically responding regions of areas 3b and 1. Onset of
either 25- or 200-Hz stimulation at a site within the cutaneous RF of a
QA neuron was accompanied by a substantial increase in mean spike
firing rate. With continued 200-Hz stimulation, however, QA neuron mean
firing rate declined rapidly (typically within 0.5-1.0 s) to a level below that recorded at the same time after onset of same-site 25-Hz
stimulation. For some neurons, the mean firing rate after the initial
0.5-1 s of an exposure to 200-Hz stimulation of the RF decreased to a
level below the level of background ("spontaneous") activity. The
decline in both the stimulus-evoked increases in absorbance in areas
3b/1 and spike discharge activity of area 3b/1 neurons within only a
few seconds of the onset of 200-Hz skin stimulation raised the
possibility that the predominant effect of continuous 200-Hz
stimulation for >3 s is inhibition of area 3b/1 QA neurons. This
possibility was evaluated at the neuronal population level by comparing
the intrinsic signal evoked in areas 3b/1 by 25-Hz skin
stimulation to the intrinsic signal evoked by a same-site skin stimulus
containing both 25- and 200-Hz sinusoidal components (a
"complex waveform stimulus"). Such experiments revealed that the
increase in absorbance evoked in areas 3b/1 by a stimulus having both
25- and 200-Hz components was substantially smaller (especially at
times >3 s after stimulus onset) than the increase in absorbance
evoked by "pure" 25-Hz stimulation of the same skin site. It is
concluded that within a brief time (within 1-3 s) after stimulus
onset, 200-Hz skin stimulation elicits a powerful inhibitory action on
area 3b/1 QA neurons. The findings appear generally consistent with the
suggestion that the activity of neurons in cortical regions other than
areas 3b and 1 play the leading role in the processing of
high-frequency (
200 Hz) vibrotactile stimuli.
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