Neural mechanisms of absolute tactile localization in monkeys

Macaca nemestrina monkeys were trained to indicate the location of suprathreshold tactile stimuli delivered to the glabrous skin of either foot. The testing paradigm involved self-initiated trials (a bar press), followed by 10-Hz stimulation at one of six locations (e.g., on the distal phalanx of the second toe on the left foot), providing the opportunity for the animal to press one of six buttons located on a facing panel. The buttons were positioned on a picture of a monkey's feet at locations corresponding to the skin loci that were stimulated on different trials. If the animal first pressed the button corresponding to the position stimulated, liquid reward was delivered; responses to any other button terminated stimulation without reward, requiring initiation of another trial for the opportunity to receive reinforcement. The localization errors for normal monkeys were reliably greater along the mediolateral dimension of the foot than they were proximodistally. For example, stimulation of the tip of toe 4 elicited responses to the button at the tip of toe 2 on 25% of the trials, as compared with only 10% errors between the tip of toe 4 and the pad at the base of toe 4. Following unilateral interruption of the dorsal spinal columns at an upper thoracic level, the capacity for absolute tactile localization was unchanged over months of testing. The greater localization accuracy along the proximodistal axis of the foot remained after dorsal column transection. In order to evaluate neural substrates of localization by monkeys, single-neuron receptive field (RF) sizes and distributions within the first somatosensory (SI) cortex were examined to determine the overlap or separation of the representations of different points on glabrous skin. The sample of neurons that provided the RF data was obtained in previous investigations of unanesthetized, neuromuscularly blocked Macaca fascicularis monkeys. Analysis of RF overlap revealed that greater than 50% of cytoarchitectural area 1 units that responded to stimulation of one digit tip also responded to another digit or to the pad at the base of a digit. These large RFs seem poorly suited to subserve a high degree of spatial localization and are compatible with the frequent localization errors by the monkeys in the behavioral experiments. However, the area 1 RF data do not explain the tendency of these animals to exhibit better localization accuracy along the proximodistal axis than along the mediolateral axis of the volar foot.(ABSTRACT TRUNCATED AT 250 WORDS)     

Prefrontal cortex and somatosensory cortex in tactile crossmodal association: an independent component analysis of ERP recordings

Our previous studies on scalp-recorded event-related potentials (ERPs) showed that somatosensory N140 evoked by a tactile vibration in working memory tasks was enhanced when human subjects expected a coming visual stimulus that had been paired with the tactile stimulus. The results suggested that such enhancement represented the cortical activities involved in tactile-visual crossmodal association. In the present study, we further hypothesized that the enhancement represented the neural activities in somatosensory and frontal cortices in the crossmodal association. By applying independent component analysis (ICA) to the ERP data, we found independent components (ICs) located in the medial prefrontal cortex (around the anterior cingulate cortex, ACC) and the primary somatosensory cortex (SI). The activity represented by the IC in SI cortex showed enhancement in expectation of the visual stimulus. Such differential activity thus suggested the participation of SI cortex in the task-related crossmodal association. Further, the coherence analysis and the Granger causality spectral analysis of the ICs showed that SI cortex appeared to cooperate with ACC in attention and perception of the tactile stimulus in crossmodal association. The results of our study support with new evidence an important idea in cortical neurophysiology: higher cognitive operations develop from the modality-specific sensory cortices (in the present study, SI cortex) that are involved in sensation and perception of various stimuli.     

Experience-dependent plasticity mechanisms for neural rehabilitation in somatosensory cortex

Functional rehabilitation of the cortex following peripheral or central nervous system damage is likely to be improved by a combination of behavioural training and natural or therapeutically enhanced synaptic plasticity mechanisms. Experience-dependent plasticity studies in the somatosensory cortex have begun to reveal those synaptic plasticity mechanisms that are driven by sensory experience and might therefore be active during behavioural training. In this review the anatomical pathways, synaptic plasticity mechanisms and structural plasticity substrates involved in cortical plasticity are explored, focusing on work in the somatosensory cortex and the barrel cortex in particular.     

Coding of tactile stimulus amplitude by neuronal ensembles in the somatosensory cortex of the rat brain

Dependence of the neuronal excitatory responses in a barrel column of the primary somatosensory cortex on the amplitude of bending of a central vibrissa within the receptive field was studied in rats. The neurons localized at a layer IV level were shown to represent a region of the hierarchically organized thalamic input to a barrel column, which possesses the highest sensitivity to the variation of the stimulus amplitude. Concept is substantiated here whereby coding of the stimulus amplitude is based on the afferent impulsation-induced modulation of a structurally preformed gradient of synaptical efficiency in the specific input to a column.Neirofiziologiya/Neurophysiology, No. 2, Vol. 27, pp. 83–92, March–April, 1995.     

Neural integration of movement: role of motor cortex in reaching

The study of the motor cortex in behaving monkeys during the past 20 years has provided important information on the brain mechanisms underlying motor control. With respect to reaching movement in space, a key role of motor cortex in specifying the direction of reaching has been proposed on the basis of results from studies of the activity of cells and cell populations during reaching. These results and ideas are reviewed and discussed in the context of recent findings concerning the spinal mechanisms underlying reaching movements.     

Neural mechanisms for color perception in the primary visual cortex

New neurophysiological results show the existence of multiple transformations of color signals in the primary visual cortex (V1) in macaque monkey. These different color mechanisms may contribute separately to the perception of color boundaries and colored regions. Many cells in V1 respond to color and to black-white (luminance) patterns. These neurons are spatially selective and could provide signals about boundaries between differently colored regions. Other V1 neurons that prefer color over luminance respond without much spatial selectivity to colored stimuli, and could be the neural basis for the response to local color modulation within a region. How these different types of color cells combine inputs from cone photoreceptors is what gives them their different spatial selectivities for color.     

Population coding in somatosensory cortex

Computational analyses have begun to elucidate which components of somatosensory cortical population activity may encode basic stimulus features. Recent results from rat barrel cortex suggest that the essence of this code is not synergistic spike patterns, but rather the precise timing of single neuron's first post-stimulus spikes. This may form the basis for a fast, robust population code.     

Habituation in the somatosensory cortex

Responses of neurons without spontaneous activity ("silent") to prolonged stimulation of the mesenteric nerves were studied in cats anesthetized with chloralose (65–70 mg/kg) and immobilized with flaxedil. The results showed that neurons of the association and primary projection areas are characterized by habituation to prolonged stimulation of visceral nerves. The rate of development of habituation depends on the parameters of stimulation and on the cortical region studied. Habituation developed more rapidly in the association area and was slower to develop at the focus of maximal activity of the second somatosensory area. The special features of cortical habituation during visceral stimulation are discussed.I. P. Pavlov Institute of Physiology, Academy of Sciences of the USSR, Leningrad. Translated from Neirofiziologiya, Vol. 11, No. 5, pp. 412–418, September–October, 1979.     

The tactile motion aftereffect revisited

In two experiments, we measured the direction, duration, frequency, and vividness of the tactile motion aftereffect (MAE) induced by a rotating drum with a ridged surface. In Experiment 1, we adapted the: (1) fingers and palm, including the thumb, (2) fingers and palm, excluding the thumb, and (3) fingers only, excluding the thumb. In each condition the drum rotated at 60 rpm for 120 s. There was no difference in duration, frequency, or vividness between the skin surfaces tested. In Experiment 2, we tested several adapting speeds: 15, 30, 45, 60, and 75 rpm. At each speed the fingers and palm, excluding the thumb, were adapted for 120 s. The duration, frequency, and vividness of the tactile MAE increased linearly with adapting speed. Overall, the tactile MAE was reported on approximately half of the trials, suggesting that it is not as robust as its visual counterpart.     

Gabrb3 is required for the functional integration of pyramidal neuron subtypes in the somatosensory cortex

1. Download : Download high-res image (143KB)
2. Download : Download full-size image

     

The prevalence of tactile motion aftereffects

The present study examined the prevalence of motion aftereffects (MAEs) in the sense of touch. The effects of two types of apparatuses were tested: a ridged, spinning cylinder and an array of vibrating tactors from the Optacon, a reading aid for the blind. In the first phase of the study, 50 subjects were tested for a total of 200 trials on both stimulators. Approximately one-third of the trials with both stimulators produced reports of MAEs in either the negative (expected) direction or the positive direction relative to the adapting stimulus. With the cylinder stimulator, there were significantly more reports of positive MAEs than negative MAEs. Subjects who reported MAEs in the first phase of the experiment were tested again in the second phase of the experiment. This additional testing produced results similar to those obtained in the first phase and did not produce a substantial increase in the number of reports of MAEs. It appears that tactile MAEs are not as readily generated as visual MAEs.     

The prevalence of tactile motion aftereffects

The present study examined the prevalence of motion aftereffects (MAEs) in the sense of touch. The effects of two types of apparatuses were tested: a ridged, spinning cylinder and an array of vibrating tactors from the Optacon, a reading aid for the blind. In the first phase of the study, 50 subjects were tested for a total of 200 trials on both stimulators. Approximately one-third of the trials with both stimulators produced reports of MAEs in either the negative (expected) direction or the positive direction relative to the adapting stimulus. With the cylinder stimulator, there were significantly more reports of positive MAEs than negative MAEs. Subjects who reported MAEs in the first phase of the experiment were tested again in the second phase of the experiment. This additional testing produced results similar to those obtained in the first phase and did not produce a substantial increase in the number of reports of MAEs. It appears that tactile MAEs are not as readily generated as visual MAEs.     

Neural circuit mechanisms for pattern detection and feature combination in olfactory cortex

Odors are initially encoded in the brain as a set of distinct physicochemical characteristics but are ultimately perceived as a unified sensory object--a "smell." It remains unclear how chemical features encoded by diverse odorant receptors and segregated glomeruli in the main olfactory bulb (MOB) are assembled into integrated cortical representations. Combining patterned optical microstimulation of MOB with in vivo electrophysiological recordings in anterior piriform cortex (PCx), we assessed how cortical neurons decode complex activity patterns distributed across MOB glomeruli. PCx firing was insensitive to single-glomerulus photostimulation. Instead, individual cells reported higher-order combinations of coactive glomeruli resembling odor-evoked sensory maps. Intracellular recordings revealed a corresponding circuit architecture providing each cortical neuron with weak synaptic input from a distinct subpopulation of MOB glomeruli. PCx neurons thus detect specific glomerular ensembles, providing an explicit neural representation of chemical feature combinations that are the hallmark of complex odor stimuli.     

Central mechanisms of tactile shape perception

Studies show that while the cortical mechanisms of two-dimensional (2D) form and motion processing are similar in touch and vision, the mechanisms of three-dimensional (3D) shape processing are different. 2D form and motion are processed in areas 3b and 1 of SI cortex by neurons with receptive fields (RFs) composed of excitatory and inhibitory subregions. 3D shape is processed in area 2 and SII and relies on the integration of cutaneous and proprioceptive inputs. The RFs of SII neurons vary in size and shape with heterogeneous structures consisting of orientation-tuned fingerpads mixed with untuned excitatory or inhibitory fingerpads. Furthermore, the sensitivity of the neurons to cutaneous inputs changes with hand conformation. We hypothesize that these RFs are the kernels underlying tactile object recognition.     

Ipsilateral median somatosensory evoked potentials recorded from human somatosensory cortex

Somatosensory evoked potentials (SEP) to ipsilateral and contralateral median nerve stimulations were recorded from subdural electrode grids over the perirolandic areas in 41 patients with medically refractory focal epilepsies who underwent evaluation for epilepsy surgery. All patients showed clearly defined, high-amplitude contralateral median SEPs. In addition, four patients showed ipsilateral SEPs. Compared with the contralateral SEPs, ipsilateral SEPs were very localized, had a different spatial distribution, were of considerably lower amplitude, had a longer latency (1.2–17.8 ms), did not show an initial negativity, and were markedly attenuated during sleep. Stimulation of the subdural electrodes overlying the sensory hand area was associated with contralateral hand paresthesias, but no ipsilateral hand paresthesias occurred. It was concluded that subdurally recorded cortical SEPs to ipsilateral stimulation of the median nerve (M) reflect unconscious sensory input from the hand possibly serving fast bimanual hand control. The anatomical pathway of these ipsilateral short-latency MSEPs is not yet known. Transcallosal transmission seems unlikely because of the short delay between the ipsilateral and contralateral responses in selected cases. The infrequent occurrence of ipsilateral subdurally recorded SEPs and their low amplitude and limited distribution suggest that they contribute very little to the short-latency ipsilateral median SEPs recorded on the scalp.