Search PubMed⌕ Search

SEARCH · Search PubMed

Results for “Somatosensory Cortex”

Search indexed PubMed citations on genomics, clinical trials, systematic reviews and public health. Explore titles, authors and supplied subject terms, then open the PubMed record.

Quote a phrase for an exact phrase match. Source license links do not imply unrestricted reuse.

At least 19 recordsLinked to original sources
PubMed1989

Quantitative study of glutamic acid decarboxylase-immunoreactive neurons and cytochrome oxidase activity in normal and partially deafferented rat hindlimb somatosensory cortex.

Somatosensory cortex reorganizes following restricted deafferentation so that deprived neurons acquire new receptive fields. Electrophysiological data suggest that a decrease in inhibition might be one of the mechanisms contributing to these changes. This hypothesis was tested by evaluating quantitatively glutamic acid decarboxylase (GAD) immunoreactivity and cytochrome oxidase (CO) activity in normal and partially deafferented rat hindlimb somatosensory cortex. In normal animals, there were laminar differences in the frequencies of GAD+ cells that correlated with the levels of CO activity. Two weeks after transection of the sciatic nerve, CO levels were reduced in all layers of the hindlimb somatosensory cortex contralateral to the nerve transection whereas the frequencies of GAD+ cells were unchanged except in layer IV where a 16% decrease was observed. This observation is consistent with the hypothesis that the expression of GAD in layer IV is partially controlled by the amount of afferent input. The ability of novel inputs to develop stable patterns of excitation in deafferented somatosensory cortex may depend upon the reduction of GABAergic inhibition which follows deafferentation.

Animals↗
PubMed2006

Magnetoencephalographic study of vibrotactile evoked transient and steady-state responses in human somatosensory cortex.

Somatosensory responses to vibrotactile stimulation applied to the index fingertip were recorded with whole-head MEG in eleven healthy young adult participants. Stimulus trains were produced by a pneumatically driven membrane oscillating at 22 Hz for a trial duration of 1 s, separated by interstimulus intervals (ISIs) of 0.5, 1.0, 3.0, and 7.0 s. Data analysis was performed in two frequency bands. Transient onset responses in the lower frequency band (<20 Hz) contained a clearly expressed P50 component. The higher frequency band (18-30 Hz) revealed a gamma-band response (GBR) within the first 200 ms followed by rhythmic activity at the stimulus frequency that continued throughout the stimulus duration, known as the steady-state response (SSR). Dipoles associated with the transient responses and SSRs were localized in two distinct regions within the primary somatosensory cortex (SI), with transient responses located on average 3 mm more medial and inferior than the SSRs. The transient and GBR peak amplitudes increased with ISI, whereas the SSR amplitude showed no ISI dependence. These results may reflect functionally and spatially distinct neural populations. Further investigations are required to assess the implications of these findings for probing the somatosensory system using other functional neuroimaging methods such as fMRI.

Adult↗
PubMed1997

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.

Adolescent↗
PubMed1999

Activation of the primary motor cortex by somatosensory stimulation in adult rats is mediated mainly by associational connections from the somatosensory cortex.

In anaesthetized adult rats, facial nerve injury causes a disinhibition of the interhemispheric connections between homotopic representation fields in the primary motor cortex with a latency of 4 min (Toldi et al., 1996, Neurosci Lett. 203, 179-182). One possible explanation for the induction of such rapid changes is an alteration of the somatosensory input to the motor cortex. To test this hypothesis, unit activity in primary motor cortex was recorded during electrical stimulation of trigeminal afferents in the contralateral whisker-pad. About one-third of all recorded primary motor cortex neurons responded with latencies shorter than in the ventrolateral and posterior nuclei of the thalamus. Responses failed at stimulation frequencies > or = 10 Hz and after elimination or inactivation of the somatosensory cortex. Within primary motor cortex, the activatable neurons displayed a bilaminar distribution and were identified as pyramidal neurons by neurobiotin labelling. The results suggest that trigeminal afferents participate in modulation of the activity of primary motor cortex output neurons via primary somatosensory cortex-to-primary motor cortex associational connections, even under anaesthesia.

Afferent Pathways↗
PubMed1995

Short-term changes of finger representation at the somatosensory cortex in humans.

The present study describes short-term modifications of the representation of the fingers at the cortex. Somatosensory evoked potentials were stimulated at the 1st, 3rd and 5th finger, and at the 1st and 5th fingers after anaesthesia of the 2nd, 3rd and 4th fingers. Somatotropic arrangement of the fingers was determined by dipole localization. After local anaesthesia significant changes of the 1st finger to lateral and of the 5th fingers to medial were found. Injection of the anaesthetic drug caused predominant burning pain at the basis of the fingers, suspected to result in a 'hyperactivation' of the connected somatosensory cortex, and giving rise to a shift of the locations towards the neighbouring cortex. This replicates results in animal studies, believed to be caused by an alteration of the excitatory-inhibitory balance at the somatosensory cortex.

Adult↗
PubMed1997

Size of somatosensory cortex and of somatosensory thalamic nuclei of the naturally blind mole rat, Spalax ehrenbergi.

The hypothesis that the somatosensory system in the naturally blind subterranean rodent Spalax ehrenbergi (= mole rat) is enlarged was tested by measuring the volume of somatosensory cortex and somatosensory thalamic nuclei (Nuclei ventrales posteromedialis and posterolateralis). Electrophysiology and tracing were used to identify and delineate these areas. On average the somatosensory cortex is 1.7 times larger and the thalamic nuclei are 1.3 times larger in the blind mole rat than in the sighted laboratory rat if different body weights are taken into consideration. This confirms the demands of a life underground where it seems touch would replace vision. The data reveal a remarkable brain plasticity among mammals under natural conditions.

Adaptation, Physiological↗
PubMed1993

[Effect of electrical stimulation of second somatosensory cortex on the response of primary somatosensory cortex to C-fiber inputs].

When the projecting point of saphenous nerve in second somatosensory cortex (S II) of cat was stimulated, the evoked potentials elicited by C-fiber inputs of saphenous nerve recorded in the primary somatosensory cortex (C-CEP) might be either inhibited or facilited according to whether the superficial and/or the deeper layer of the cortex was stimulated. The inhibition was expressed as a decrease of amplitude and prolongation of latency of C-CEP; while the facilitation, as an increase of amplitude and duration of C-CEP. When the superfaicial layer of S II was stimulated by weaker current, both inhibitory and facilitatory effects could be observed, but only inhibitory effect was observed, when the deep layer was stimulated. With the same intensity of stimulation, inhibitory effect was more pronounced when the deep layer rather than the superficial layer was stimulated. It is suggested that S II may play a role in the modulation of C-CEP of S I.

Animals↗
PubMed1979

Loss of hybridizable ribosomal DNA from human post-mitotic tissues during aging: II. Age-dependent loss in human cerebral cortex--hippocampal and somatosensory cortex comparison.

DNA was isolated from the hippocampal and from the somatosensory cortex of 13 humans (at autopsy). In both the cortex and hippocampus, the loss of ribosomal DNA (rDNA), as measured through hybridization in the liquid phase, approximates about 0.9% per year. The r value for somatosensory cortex was about -0.7 and that for the hippocampus was about -0.91. The correlation coefficient between the sets of two samples derived from the same individual (two different areas) in +0.945. These results are consistent with those reported concurrently for human myocardium and with earlier studies conducted with beagle dogs, in which only post-mitotic tissues (brain, heart and skeletal muscle) showed measurable decrements in these key genes. To the degree that the synthesis of new proteins is essential for sustained mental activity, these results are consistent with the observations that Nissl substance is more slowly replenished, following exhaustive work by motor cortical cells, and the fact that many older persons experience mental fatigue during continuous mental work at earlier times than do younger persons. The mechanism of loss is not certain, but may well be related to inadequacies in DNA repair systems, thereby allowing deletion of tandemly duplicated genes through cross-over "episome" formation, followed by degradation of the excised DNA segments. The ratio of loss of rDNA hybridizability in human and dogs in about 1 to 7, which approximates the relative ratios of their lifespans (reciprocals).

Adolescent↗
PubMed1995

Induction of long-lasting potentiation in the secondary somatosensory cortex by thalamic stimulation requires cortico-cortical pathways from the primary somatosensory cortex.

We have investigated the role of cortico-cortical inputs from the primary somatosensory cortex in the induction of long-lasting potentiation in the secondary somatosensory cortex. Long-lasting potentiation of evoked potentials in the feline secondary somatosensory cortex is induced by high frequency stimulation of the ventral posterolateral thalamic nucleus. The secondary somatosensory cortex receives two projections from the ventral posterolateral thalamic nucleus; a direct pathway from the ventral posterolateral thalamic nucleus and a cortico-cortical pathway via the primary somatosensory cortex. The present study was designed to examine dominance of these pathways in the induction of long-lasting potentiation in the secondary somatosensory cortex. Long-lasting potentiation was evaluated by changes in the amplitude of field potentials and current source densities elicited by ventral posterolateral thalamic nucleus test stimulation (0.1 Hz) following conditioning stimulation. The conditioning stimulation, consisting of 20 trains of 200 Hz bursts, was delivered to the ventral posterolateral thalamic nucleus or the primary somatosensory cortex. Field potentials in the secondary somatosensory cortex were simultaneously recorded at 16 points placed vertically at 150 microns intervals from the cortical surface and current source density was computed using these field potentials. First, we blocked inputs from the primary somatosensory cortex to the secondary somatosensory cortex by intracortical injection of lidocaine into the primary somatosensory cortex. The amplitudes of the field potentials recorded in the secondary somatosensory cortex diminished within 5 min after lidocaine injection. Current source density analysis showed a marked decrease in the sink currents in layers II/III (at depths of 450-600 microns).(ABSTRACT TRUNCATED AT 250 WORDS)

Anesthetics, Local↗
PubMed2001

The distribution of mislocalizations across fingers demonstrates training-induced neuroplastic changes in somatosensory cortex.

The somatosensory system has been shown to alter its cortical activation patterns in reaction to changes in the attended sensory input to certain body parts. Whether these modifications in the functional organization of the somatosensory cortex of humans also result in perceptual changes has rarely been investigated. Here we used near-threshold tactile stimuli to the center of the fingertips to evoke mislocalizations to fingers other than the stimulated. In healthy untrained subjects, the distribution of the mislocalizations from each of the fingers was different from a distribution expected if the subjects were purely guessing the position of the stimulus. The digits next to the stimulated one receive a higher number of mislocalizations than digits further away from the stimulated digits. This decrease can be accounted for by digit-overlapping receptive fields in combination with the sequential representation of the digits in the primary somatosensory cortex. In a second experiment subjects received 20 h of simultaneous stimulation of the left thumb and little finger in the context of a perceptual task. For both hands, the distribution of mislocalization from these fingers was analyzed at the beginning and the end of the training. For the left hand, the number of assigned mislocalizations to the most distant neighbor digit (i.e., the simultaneously stimulated digit in the training) increased while the number of mislocalizations toward the direct neighboring digit decreased with the training. This change did not occur in the untrained right hand, or in the untrained subjects. We conclude that the distribution of mislocalization to fingers other than the stimulated can be used to investigate perceptual changes paralleling training-induced modifications in the activation patterns of the somatosensory cortex.

Adult↗
PubMed1994

Release of GABA following a single whisker stimulation in the adjacent barrels of rat somatosensory cortex.

The somatosensory cortex of rodents contains discrete groups of neurons in layer IV, called barrels, which are related in a one-to-one fashion to individual vibrissae. In order to examine the effect of a single vibrissa stimulation on the release of GABA in the barrel cortex, GABA was measured by brain microdialysis in the barrel cortex of anesthetized rats. The basal level of endogenous GABA release was 0.15 +/- 0.05 pmol/30 microliters dialysate (n = 15). Stimulation of a single vibrissa gave rise to a marked increase in GABA release above the basal level (80 +/- 56% of basal level, n = 8). Effects were limited to a single barrel representing the stimulated single vibrissa. The stimulus-evoked GABA release was completely suppressed by 10 microM TTX, while the basal release of GABA was not affected by TTX. Vibrissa stimulation often caused a significant decrease in the basal level of GABA in the neighboring barrel. These results suggest that the release of GABA evoked by a single vibrissa stimulation is regulated by an inter-barrel mechanism in the rat barrel cortex.

Animals↗
PubMed1991

Somatosensory cortex of the neonatal pig: II. Topographic organization of the secondary somatosensory cortex (SII).

Multiunit microelectrode recording techniques were used to delineate the somatotopic organization of the secondary somatosensory cortex (SII) of the neonatal pig. Barbiturate anesthetized piglets ranging in age from 7 days preterm to 2 months postpartum were used. The SII area, located lateral to the rostral and middle suprasylvian sulci, was found to contain a complete somatotopic representation of the contralateral body surface with a significant proportion of bilateral input for all body regions except the forehoof and forelimb. The SII forelimb and hindlimb representations were found to possess a "striplike" orientation in a rostral to caudal sequence, and the trunk representation was located posterolateral to the hindlimb representation, giving SII an inverted appearance. Two apparently separate face representations were delineated; one posterolateral to the projection from the trunk and the other anterior to the forehoof region. Unlike SI, which possesses a disproportionately large representation of the rostrum, SII has no specialized representation of the rostrum. The overall organization of SII supports the contention that this cortical region provides a more generalized representation of the entire body surface than does SI.

Animals↗
PubMed1991

Somatosensory cortex of the neonatal pig: I. Topographic organization of the primary somatosensory cortex (SI).

The cerebral cortex of adult mammals contains several somatotopic representations of the body surface. Although the organization of the various somatosensory cortices of numerous species of adult animals has been elucidated, data on the somatosensory representations of fetal and neonatal animals are limited. As part of an investigation into the perinatal development of the somatosensory cortices, it was necessary to delineate the organization of the somatosensory cortices of the perinatal pig. This study presents the topographical organization of the primary somatosensory cortex (SI) of the perinatal pig. Multiunit microelectrode mapping methods were used to produce topographic maps of SI from barbiturate anesthetized pigs ranging in age from 7 days preterm to 2 months postpartum. It was demonstrated that the overall organization of this region of cortex was similar to that of other mammals: a somatotopic projection of predominantly the contralateral body surface was delineated in which the hindlimb is represented medially and the face laterally across the cortex. A disproportionately enlarged rostrum representation was mapped in detail, and multiple representations of the rostrum, face, and mouth were found. Several of these representations exhibited bilateral and ipsilateral input. The SI trunk and hindlimb representations were located on the medial wall of the hemisphere; these representations were small but their presence refutes speculation that ungulates do not have a complete body representation in SI.

Animals↗
PubMed2003

Gamma synchronization in human primary somatosensory cortex as revealed by somatosensory evoked neuromagnetic fields.

Cortical sensory neurons synchronize their activity at multiple frequency bands after an external stimulation. In the somatosensory cortical areas, previous reports describe more discrete and somatotopically specific neural synchronization at the gamma band. Therefore, an efficient gamma synchronization of the neurons in primary somatosensory cortex (S1) may be expected to characterize the stimulus processing from the thumb, i.e. the hand's most skillful area. To test this hypothesis, neuromagnetic fields were evoked over human S1 by the electrical stimulation of the contralateral thumb or little finger. Neuronal synchronization was indexed by the spectral coherence of the evoked neuromagnetic fields overlying S1. The frequencies of interest were the beta (16-32 Hz) and gamma (36-46 Hz) bands. The global amount of the coherence was defined as the total event-related coherence (ERCoh) among all magnetic sensors overlying the S1. Results showed prevalent increment of beta ERCoh (20-32 Hz) after the little finger stimulation and of gamma ERCoh (36-44 Hz) after the thumb stimulation. These results suggest that the neural synchronization in S1, as revealed by the ERCoh, may vary in frequency as a function of the finger stimulated. In this framework, the neural synchronization at gamma band may characterize the cortical representation of thumb, functionally prevalent with respect to little finger in humans.

Afferent Pathways↗
PubMed1989

Comparison of behavioral effects of nucleus basalis magnocellularis lesions and somatosensory cortex ablation in the rat.

Cholinergic neurons in the nucleus basalis region of the forebrain project to various portions of the cerebral cortex, including somatosensory cortex. Degeneration of these neurons and their cortical projections is a major feature of the neuropathology of Alzheimer's disease. Injecting an excitotoxin into the basal forebrain to destroy nucleus basalis neurons provides a potentially useful animal model for studying the role of these neurons in Alzheimer's disease. Previously, we demonstrated that rats with nucleus basalis excitotoxin lesions performed poorly on a tactile discrimination task and on a test of working memory. In an effort to clarify further the role of impaired memory versus other types of impairment (e.g. disrupted somatosensory processing due to cholinergic deafferentation of somatosensory cortex), we compared a group of rats with bilateral nucleus basalis excitotoxin lesions and a group with bilateral somatosensory cortical ablations on a variety of behavioral tasks. Rats with nucleus basalis lesions performed as well as controls on a battery of neurological tests but exhibited increased emotionality unlike rats with somatosensory cortical ablations which performed poorly on the battery but were not hyperemotional. The two lesion groups were impaired significantly and to a comparable degree in performing two-choice tactile discriminations in a T-maze. In contrast, only rats with nucleus basalis lesions showed deficits in working memory as tested in an eight-arm radial maze. Both lesion groups performed comparably to sham controls on a test of reference memory involving a black/white discrimination in a T-maze. The findings suggest that rats with nucleus basalis lesions manifest disturbances in several of the same spheres (emotionality, somatosensory information processing, memory) that are disrupted in Alzheimer's disease and further confirm the utility of the excitotoxin lesion approach for studying the pathophysiology of Alzheimer's disease.

Animals↗
PubMed1998

Loss of adenylyl cyclase I activity disrupts patterning of mouse somatosensory cortex.

The somatosensory (SI) cortex of mice displays a patterned, nonuniform distribution of neurons in layer IV called the 'barrelfield' (ref. 1). Thalamocortical afferents (TCAs) that terminate in layer IV are segregated such that each barrel, a readily visible cylindrical array of neurons surrounding a cell-sparse center, represents a distinct receptive field. TCA arbors are confined to the barrel hollow and synapse on barrel-wall neurons whose dendrites are oriented toward the center of the barrel. Mice homozygous for the barrelless (brl) mutation, which occurred spontaneously in ICR stock at Université de Lausanne (Switzerland), fail to develop this patterned distribution of neurons, but still display normal topological organization of the SI cortex. Despite the absence of barrels and the overlapping zones of TCA arborization, the size of individual whisker representations, as judged by 2-deoxyglucose uptake, is similar to that of wild-type mice. We identified adenylyl cyclase type I (Adcy1) as the gene disrupted in brl mutant mice by fine mapping of proximal chromosome 11, enzyme assay, mutation analysis and examination of mice homozygous for a targeted disruption of Adcy1. These results provide the first evidence for involvement of cAMP signalling pathways in pattern formation of the brain.

Adenylyl Cyclases↗
PubMedDate not supplied

Long-term increases in neuronal activity in the motor cortex evoked by simultaneous stimulation of the thalamus and somatosensory cortex in cats.

Experiments on anesthetized cats were used to study the activity of motor cortex neurons (field 4 gamma) in response to separate and simultaneous stimulation of the ventrolateral nucleus of the thalamus and the somatosensory cortex (field 2) of the brain. Long-term potentiation of motor cortex neuron activity in response to simultaneous stimulation of the ventrolateral nucleus and somatosensory cortex arose only in regions receiving corticocortical projections from the stimulation site in the somatosensory cortex of the brain, while regions lacking corticocortical projections from the somatosensory cortex showed no such effect. Experiments demonstrated that the duration of increased motor cortex neuron activity following stimulation of the ventrolateral nucleus of the thalamus and somatosensory cortex was greater than one hour after recording was started. These data led to the conclusion that simultaneous stimulation of corticocortical and thalamocortical afferents can alter the level of neuronal activity in the motor cortex only in regions with convergent sensory inputs from the thalamus and somatosensory cortex of the brain.

Action Potentials↗
PubMed1986

Somatosensory evoked potentials after removal of somatosensory cortex in man.

Somatosensory evoked potentials (SEPs) to median nerve, ulnar nerve, thumb, middle finger, and posterior tibial nerve stimulation were recorded in a patient with a discrete resection of part of the postcentral somatosensory cortex as a treatment for focal epilepsy. Comparison of the different stimulation sites confirmed electrophysiologically the restricted locus of the lesion. The results strongly suggest that the early negative component (N20) and subsequent components recorded postcentrally are of cortical origin and depend upon postcentral gyrus cytoarchitectonic areas 3, 2, and 1. Moreover, these postcentral SEPs are distinct from precentrally recorded activity.

Adult↗