Human Somatosensory Areas Research Articles

Decoding pressure stimulation locations on the fingers from human neural activation patterns.

In this functional MRI study, we investigated how the human brain activity represents tactile location information evoked by pressure stimulation on fingers. Using the searchlight multivoxel pattern analysis, we looked for local activity patterns that could be decoded into one of four stimulated finger locations. The supramarginal gyrus (SMG) and the thalamus were found to contain distinct multivoxel patterns corresponding to individual stimulated locations. In contrast, the univariate general linear model analysis contrasting stimulation against resting phases for each finger identified activations mainly in the primary somatosensory cortex (S1), but not in SMG or in thalamus. Our results indicate that S1 might be involved in the detection of the presence of pressure stimuli, whereas the SMG and the thalamus might play a role in identifying which finger is stimulated. This finding may provide additional evidence for hierarchical information processing in the human somatosensory areas.

Adaptation in human somatosensory cortex as a model of sensory memory construction: a study using high-density EEG.

Adaptation in sensory cortices has been seen as a mechanism allowing the creation of transient memory representations. Here we tested the adapting properties of early responses in human somatosensory areas SI and SII by analysing somatosensory-evoked potentials over the very first repetitions of a stimulus. SI and SII generators were identified by well-defined scalp potentials and source localisation from high-density 128-channel EEG. Earliest responses (~20 ms) from area 3b in the depth of the post-central gyrus did not show significant adaptation to stimuli repeated at 300 ms intervals. In contrast, responses around 45 ms from the crown of the gyrus (areas 1 and 2) rapidly lessened to a plateau and abated at the 20th stimulation, and activities from SII in the parietal operculum at ~100 ms displayed strong adaptation with a steady amplitude decrease from the first repetition. Although responses in both SI (1-2) and SII areas showed adapting properties and hence sensory memory capacities, evidence of sensory mismatch detection has been demonstrated only for responses reflecting SII activation. This may index the passage from an early form of sensory storage in SI to more operational memory codes in SII, allowing the prediction of forthcoming input and the triggering of a specific signal when such input differs from the previous sequence. This is consistent with a model whereby the length of temporal receptive windows increases with progression in the cortical hierarchy, in parallel with the complexity and abstraction of neural representations.

Functional Lateralization of Face, Hand, and Trunk Representation in Anatomically Defined Human Somatosensory Areas

We used functional magnetic resonance imaging (fMRI) and cytoarchitectonic probability maps to investigate the responsiveness of individual areas in the human primary and secondary somatosensory cortices to hand, face, or trunk stimulation of either body-side. A Bayesian modeling approach to quantify the probability of ipsilateral activations revealed that areas OP 1, OP 4, and OP 3 of the SII cortex as well as the trunk and face representations within all SI subareas (areas 3b, 1, and 2) show robust bilateral responses to unilateral stimulation. Such bilateral response properties are in good agreement with the transcallosal projections demonstrated for these areas in nonhuman primates and other mammals. In contrast, the SI hand region showed a different pattern. Whereas ipsilateral areas 3b and 1 were deactivated by tactile hand stimulation, particularly on the left, there was strong evidence for ipsilateral processing of information from the right hand in area 2. These results demonstrate not only the behavioral importance of the hand representation, but also suggest that area 2 may have particularly evolved to form the cortical substrate of these specialized demands, in line with recent studies on cortical evolution hypothesizing that area 2 has developed with increasing manual abilities in anthropoid primates featuring opposable thumbs.

Functional connectivity between forearm and digits representations in human somatosensory area 3b

Objective: We compared the effects of tactile interference to the forearm on magnetic responses evoked by electric stimulation of the little finger (D5) and the thumb (D1). Methods: Electric stimulation was delivered to D5 or D1 individually. In each stimulus session, magnetic recordings were conducted with or without concurrent tactile interference to the radial side of the anterior forearm. Results: With forearm interference, the amplitude of the primary response (N20m) following D5 stimulation was reduced to 90.7% of the control value without interference, while that following D1 stimulation was not affected (100.7%). Conclusions: In human somatosensory area 3b, the representation of the forearm is immediately adjacent to that of the D5, and distant from that of the D1. Thus, the result suggests that the tactile interference effect on N20m depends on the cortical distance between electrically and mechanically activated 3b areas. Significance: Intrinsic synaptic connections between the 3b hand representation and its surroundings have been hypothesized as a neural basis for plastic changes of the human brain, such as a phantom hand phenomenon. The present finding implies that these connections may play some physiological roles even in normal adult humans.

Tactile interference to the face affects magnetic responses elicited by electric thumb stimulation.

We examined the effect of tactile interference to the face on somatosensory evoked magnetic fields (SEFs) following electric thumb stimulation. SEFs were elicited by electric stimulation of the right thumb in a control and two interference conditions. In the interference conditions, continuous tactile stimuli were delivered to the skin surface over the right upper face or the right thumb. The face interference significantly attenuated N20m and enhanced P30m. The amplitudes of N20m in the face and thumb interference conditions were 90.3 and 70.3% of the value in the control condition, respectively, while those of P30m were 120.2 and 74.4%. In human somatosensory area 3b, the representation of the thumb is immediately adjacent to that of the face although the thumb and face are physically distant. We suggest, therefore, that the effect of tactile interference on N20m depends on a cortical distance between electrically and mechanically activated 3b areas, rather than a physical distance between the body parts to which these two stimuli were administered. Although it is unclear why the face interference specifically enhanced the P30m, it is suggested that the generating mechanism of the interference effect on P30m may be different from that on N20m. The tactile interference effect on N20m does not depend on the physical distance between electrically and mechanically activated skin areas, but on the distance of the 3b cortex receiving these two inputs.

Effect of interstimulus interval on attentional modulation of cortical activities in human somatosensory areas.

To investigate the effect of interstimulus interval (ISI) on attentional enhancement of cortical activity in human somatosensory cortices. Somatosensory magnetic fields (SEFs) evoked by electrical stimulation of the right median nerve at ISIs of 0.5, 1, 3 and 5 s were recorded in two separate conditions by using whole head type magnetoencephalography. In the attend-condition: subjects directed attention to the stimuli by watching the stimulated body site and mentally counting the stimuli. In the ignore-condition: subjects ignored the stimuli by reading a book. Attention to the tactile stimulation amplified SEFs in contralateral secondary (SIT) at ISIs of 1, 3 and 5 s and in ipsilateral SII at ISI of 5 s. There was no effect of attention on the SEF in primary. The ratios of the equivalent current dipole moments calculated for the attend-condition compared to ignore-condition were 1.49 +/- 0.14 at ISI of 1 s, 1.47 +/- 0.29 at 3 s and 1.34 +/- 0.23 at 5 s in the contralateral SII and 1.40 +/- 0.24 at 5 s in the ipsilateral SII. Time longer than 0.5 s might be required for active attention genesis and, after it was generated, the cortical activation in the attend condition was proportional to the activity in the ignore condition.

Integration of microstructural and functional aspects of human somatosensory areas 3a, 3b, and 1 on the basis of a computerized brain atlas.

In this study we analyzed structural and functional aspects of the human primary somatosensory areas 3a, 3b, and 1 on the basis of a computerized brain atlas. The approach overcomes many of the problems associated with subjective architectonic parcellations of the cortex and with 'classical" brain maps published in a "rigid" print format. Magnetic resonance (MR) scans were obtained from ten postmortem brains. The brains were serially sectioned at 20 microm, and sections were stained for cell bodies. Areas 3a, 3b, and 1 were delineated statistically on the basis of differences in the laminar densities of neuronal cell bodies. The borders of the areas were topographically variable across different brains and did not match macroanatomical landmarks of the postcentral gyrus. After correction of the sections for deformations due to histological processing, each brain's 3-D reconstructed histological volume and the volume representations of areas 3a, 3b, and 1 were adapted to the reference brain of a computerized atlas and superimposed in 3-D space. For each area, a population map was generated that described, for each voxel, how many brains had a representation of that area. Despite considerable interindividual variability, representations of areas 3a, 3b, and 1 in > or = 50% of the brains were found in the fundus of the central sulcus, in the rostral bank, and on the crown of the postcentral gyrus, respectively. For each area, a volume of interest (VOI) was defined that encompassed that area's representation in > or = 50% of the brains. Despite close spatial relationship in the postcentral gyrus, the three VOIs overlapped by < 1% of their volumes. Changes in regional cerebral blood flow (rCBF) were measured with positron emission tomography when six right-handed subjects discriminated differences in the speed of a rotating brush stimulating the palmar surface of the right hand. With co-registered MR images, the rCBF data were adapted to the same reference brain and superimposed with the microstructural VOIs. Discrimination of moving stimuli, contrasted to rest, increased the rCBF in the VOIs of areas 3b and 1, but not in area 3a. This approach opens up the possibility of (1) defining VOIs of cortical areas which are not based on macroanatomical landmarks but instead on observer-independent cytoarchitectonic mapping of postmortem brains and of (2) determining in these VOIs changes in rCBF data obtained from functional imaging experiments.

Human Somatosensory Area 2: Observer-Independent Cytoarchitectonic Mapping, Interindividual Variability, and Population Map

We analyzed the topographical variability of human somatosensory area 2 in 10 postmortem brains. The brains were serially sectioned at 20 μm, and sections were stained for cell bodies. Area 2 was delineated with an observer-independent technique based on significant differences in the laminar densities of cell bodies. The sections were corrected with an MR scan of the same brain obtained before histological processing. Each brain's histological volume and representation of area 2 was subsequently reconstructed in 3-D. We found that the borders of area 2 are topographically variable. The rostral border lies between the convexity of the postcentral gyrus and some millimeters deep in the rostral wall of the postcentral sulcus. The caudal border lies between the fundus of the postcentral sulcus and some millimeters above it in the rostral wall. In contrast to Brodmann's map, area 2 does not extend onto the mesial cortical surface or into the intraparietal sulcus. When the postcentral sulcus is interrupted by a gyral bridge, area 2 crosses this bridge and is not separated into two segments. After cytoarchitectonic analysis, the histological volumes were warped to the reference brain of a computerized atlas and superimposed. A population map was generated in 3-D space, which describes how many brains have a representation of area 2 in a particular voxel. This microstructurally defined population map can be used to demonstrate activations of area 2 in functional imaging studies and therefore help to further understand the role of area 2 in somatosensory processing.