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The Journal of Neurophysiology Vol. 83 No. 3 March 2000, pp. 1158-1166
Copyright ©2000 by the American Physiological Society
1Department of Mathematics, University of Pittsburgh; and 2Department of Neurobiology, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania 15261
Pinto, David J.,
Joshua C. Brumberg, and
Daniel J. Simons.
Circuit Dynamics and Coding Strategies in Rodent
Somatosensory Cortex. J. Neurophysiol. 83: 1158-1166, 2000. Previous experimental studies of both cortical barrel and
thalamic barreloid neuron responses in rodent somatosensory cortex have
indicated an active role for barrel circuitry in
processing thalamic signals. Previous modeling studies of the
same system have suggested that a major function of the barrel circuit
is to render the response magnitude of barrel neurons
particularly sensitive to the temporal distribution of
thalamic input. Specifically, thalamic inputs that are initially
synchronous strongly engage recurrent excitatory connections in the
barrel and generate a response that briefly withstands the strong
damping effects of inhibitory circuitry. To test this experimentally,
we recorded responses from 40 cortical barrel neurons and 63 thalamic
barreloid neurons evoked by whisker deflections varying in velocity and amplitude. This stimulus evoked thalamic response profiles that varied
in terms of both their magnitude and timing. The magnitude of the
thalamic population response, measured as the average number of evoked
spikes per stimulus, increased with both deflection velocity and
amplitude. On the other hand, the degree of initial synchrony, measured
from population peristimulus time histograms, was highly correlated
with the velocity of whisker deflection, deflection amplitude having
little or no effect on thalamic synchrony. Consistent with the
predictions of the model, the cortical population response was
determined largely by whisker velocity and was highly correlated with
the degree of initial synchrony among thalamic neurons
(R2 = 0.91), as compared with the
average number of evoked thalamic spikes
(R2 = 0.38). Individually, the response
of nearly all cortical cells displayed a positive correlation with
deflection velocity; this homogeneity is consistent with the dependence
of the cortical response on local circuit interactions as proposed by
the model. By contrast, the response of individual thalamic neurons
varied widely. These findings validate the predictions of the modeling studies and, more importantly, demonstrate that the mechanism by which
the cortex processes an afferent signal is inextricably linked with,
and in fact determines, the saliency of neural codes embedded in the
thalamic response.
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