1. Extracellular single-unit recordings and controlled whisker stimuli were used to compare response properties between cells in the "barreloids" of the thalamic ventrobasal complex and those in the cytochrome oxidase-rich centers of the "barrels" in the first somatic sensory cortex. Individual vibrissae were deflected alone or in paired combination involving the neuron's maximally excitatory whisker and an adjacent one in the same or neighboring whisker rows. Quantitative data were derived from 135 thalamocortical unit's (TCUs), 242 "regular-spike" barrel units (RSUs), and 16 "fast-spike" barrel units (FSUs) recorded in 26 normal adult rats. 2. Compared with TCUs, RSUs displayed lower rates of spontaneous activity and responded less vigorously to whisker stimuli. Proportionally, more than twice as many TCUs as RSUs responded in slowly adapting fashion to at least one angular direction of whisker displacement. Discharges of slowly adapting TCUs were approximately 3.5 times greater than those of slowly adapting RSUs. 3. Proportionally, about twice as many TCUs than RSUs responded selectively to whisker movements in different angular directions. 4. Cells in the thalamus responded more vigorously to a larger number of whiskers than RSUs in the cortex. Depending on the stimulus conditions, two to three times more TCUs than RSUs were excited by two or more whiskers. 5. Following displacement of an adjacent whisker, unit discharges to subsequent deflections of the maximally excitatory whisker were reduced in a time-dependent fashion. The time course of response suppression was similar in TCUs and RSUs, but inhibitory interactions between adjacent whiskers were observed much less often in the thalamus. A cyclic pattern of stimulus-evoked excitation/inhibition characterizes responses in the cortical barrels but is considerably less pronounced in the thalamic barreloids. 6. The presence and/or degree of response suppression depended on which adjacent whisker was stimulated and on the angular direction of that whisker's movement. For individual TCUs, some adjacent whiskers evoked inhibition, others did not. The vast majority of RSUs displayed response suppression to all adjacent whiskers. Unlike receptive fields of TCUs, those of RSUs have small--i.e., single-whisker--excitatory centers with potent and symmetrical inhibitory surrounds. 7. Fast-spike units in the barrels displayed the greatest spontaneous and stimulus-evoked activities and were the least selective for whisker movements at different angular directions. FSUs had the largest excitatory receptive fields; 100% responded to two or more vibrissae.(ABSTRACT TRUNCATED AT 400 WORDS)
The response properties of 123 trigeminal ganglion neurons were studied, using controlled whisker deflections in different directions. When the distal end of the whisker was initially displaced 5.7 degrees (1 mm) from its neutral position, 81% of the cells responded with statistically more spikes/stimulus to movements in one to three of eight cardinal (45 degrees increment) directions than to the others. The more directionally selective the cell, the more vigorous was its response. On the basis of statistical criteria, 75% of the cells were classified as slowly adapting, 25% as rapidly adapting. A number of quantitative analyses indicated that slowly adapting units respond more selectively than rapidly adapting cells to the direction of whisker movement. Differences in directional sensitivities of rapidly and slowly adapting cells appear to parallel differences between their putative mechanoreceptive endings and the relationships between those endings and the vibrissa follicle's structure. Comparisons between the response properties of peripheral and central neurons in the vibrissa-lemniscal system indicate that the afferent neural signal is progressively and substantially transformed by mechanisms that function to integrate information from different peripheral receptors and from different, individual vibrissae.
Axonal tracing techniques were used to examine the distribution of corticothalamic projection neurons in relation to the organization of the thalamocortical recipient zones in the whisker representation of the rat first somatic sensory cortex. Following injection of horseradish peroxidase into the physiologically defined vibrissa area in the ventrobasal complex of the thalamus, labeling in the cortex had a columnar appearance. Dense patches of anterograde labeling were located within the centers of the layer IV barrels and extended superficially through lamina III; the septa between barrels contained considerably less reaction product. Retrogradely labeled neurons were observed in lower layer V and layer VI where they were concentrated preferentially deep to the barrel centers. Regions deep to the septa displayed less overall labeling and a lower relative number of thalamic projecting neurons. Zones having the larger numbers of retrogradely labeled cells also contained terminallike labeling of either corticothalamic or thalamocortical origin. Following an injection that included the posterior group medial to the ventrobasal complex, anterograde labeling in layer IV was located largely in the septa. In conjunction with previous findings concerning the origin and termination of other projection systems in the barrel cortex, these results suggest that a vibrissal column contains a central core zone intimately linked with the ventrobasal thalamus that is bounded by narrower regions of more diverse inputs and outputs that form an interface between adjacent cortical columns.
A prominent feature of thalamocortical circuitry in sensory systems is the extensive and highly organized feedback projection from the cortex to the thalamic neurons that provide stimulus-specific input to the cortex. In lightly sedated rats, we found that focal enhancement of motor cortex activity facilitated sensory-evoked responses of topographically aligned neurons in primary somatosensory cortex, including antidromically identified corticothalamic cells; similar effects were observed in ventral posterior medial thalamus (VPm). In behaving rats, thalamic responses were normally smaller during whisking but larger when signal transmission in brainstem trigeminal nuclei was bypassed or altered. During voluntary movement, sensory activity may be globally suppressed in the brainstem, whereas signaling by cortically facilitated VPm neurons is simultaneously enhanced relative to other VPm neurons receiving no such facilitation.The somatosensory system intimately cooperates with the motor system during tactile exploration and active touch. In the whisker sensorimotor system of rats, extensive interconnections exist between sensory and motor neural subsystems 1 . During whisking, motor cortex activity is elevated 2 , but sensory-evoked responses in the lemniscal system are typically attenuated 3-7 .Motor cortex projections to deep layers of primary somatosensory cortex (S1) can potentially excite corticothalamic cells either mono-synaptically or by local circuit interactions 8,9 . S1 corticothalamic neurons are thus strategically positioned to regulate activity in thalamocortical circuits during voluntary movement 9 . Corticothalamic feedback can enhance thalamic firing and response tuning 10,11 . The circumstances in which corticothalamic neurons are engaged are not yet known. A substantial proportion of corticothalamic cells are weakly responsive or even silent in anesthetized 12,13 and awake animals 14-17 .We found that S1 corticothalamic neurons in whisker/barrel cortex responded more robustly to whisker deflections when motor cortex activity was focally enhanced. Similar effects were observed in topographically aligned thalamic neurons in the VPm. Thus, corticothalamocortical circuitry is engaged by other functionally related cortical centers. During whisking in behaving rats, VPm responses were suppressed when whisker follicles were stimulated but were enhanced when processing in brainstem nuclei was bypassed or experimentally altered.
Rats explore objects by rhythmically whisking them with their mystacial vibrissae. On two types of tactile discrimination tasks, macrogeometric and microgeometric, better performers palpated the discrimnanda for longer periods of time and used movement patterns that appeared to optimize whisking frequency bandwidth and the extent to which the vibrissae would be bent by object contact. On a task involving finely textured surfaces, good and poor performers differed in the temporal components of their whisking patterns, whereas the spatial domain was more important for animals palpating surfaces with widely separated features. These findings are consistent with increasing neurophysiological evidence that the central representation of the tactile periphery, in rodents and other mammals, is both integrative and dynamic.
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