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Biomedical subjects

M Ptito

Publications and source records attributed to M Ptito.

At least 19 recordsLinked to original sources

Somatosensory receptive field properties of corpus callosum fibres in the raccoon.

Anatomical studies in a number of species have shown that most areas of the somatosensory cortex are callosally interconnected. This is also true for the raccoon, at least for those parts representing proximal and axial body regions. Electrophysiologically, studies carried out in cats and monkeys have demonstrated that all sensory sub-modalities cross in the callosum. Moreover, cells representing the paws and fingers, though occupying a large portion of areas SI and SII, seem to send proportionately fewer axons through the callosum than axial structures. No comparable study has been carried out in the raccoon. The purpose of the present experiment was therefore to investigate the functional organization of the callosal system in this animal by examining the receptive field properties of the somatosensory fibres crossing in the callosum. Axonal activity was recorded directly through tungsten microelectrodes in the corpus callosum of eight raccoons. Results indicated that somatosensory information is transmitted in its rostral portion. Most receptive fields concerned axial and proximal body regions and the head and face. Some receptive fields represented para-axial regions of the body and a few concerned the hands and fingers. Slowly and rapidly adapting fibres were found, as were all the sensory sub-modalities tested. A substantial proportion of the axons had bilateral receptive fields. These results are discussed in relation to those obtained in other species, with particular reference to: (1) the midline fusion hypothesis of callosal function; (2) the representation within this structure of the distal extremities, and (3) the origin of the bilateral receptive fields.

Animals

Binocular interaction and disparity coding at the 17-18 border: contribution of the corpus callosum.

Binocular disparity, resulting from the projection of a three-dimensional object on the two spatially separated retinae, constitutes one of the fundamental cues for stereoscopic perception. The binocularity of cells in one hemisphere stems from two sources: i) from the ipsilateral ganglion cells in the temporal retina which converge with inputs coming from the contralateral nasal retina; the latter axons cross at the chiasma; ii) from inputs originating in the opposite hemisphere which cross in the corpus callosum. The objective of this study was to demonstrate that interactions from both types of inputs can result in the formation of disparity sensitive neurons and presumably that either type could mediate stereoperception based on disparity cues. Two types of disparity sensitive neurons were found in the normal cat: one type, showing maximal interactive effects around zero disparity responded with strong excitation or inhibition when the stimuli were in register. These neurons are presumed to signal stimuli situated about the fixation plane. The other type, also made up of two subtypes of opposed valencies, gave maximum responses at one set of disparities and inhibitory responses to the other set. These were presumed to signal stimuli situated in front of or behind the fixation plane. In the split-chiasm cat, whose cortical binocularity is presumably assured by converging ipsilateral and callosal inputs, three of the four subtypes of disparity sensitive neurons were found, the uncrossed disparity cells being absent in these animals. Moreover, stimulating each eye individually indicated that nearly 80% of the cells in normal and about 40% in split-chiasm cats were binocularly driven. However, both these figures underestimated the amount of binocular interaction in the callosal recipient zone, since stimulating both eyes simultaneously showed that a proportionately larger number of cells were binocularly driven. Disparity sensitive cells also varied as a function of ocular dominance, i.e., cells signaling the fixation plane tended to have balanced dominance whereas units preferring stimuli situated in front of or behind the fixation plane were dominated by the ipsilateral and contralateral eyes, respectively.

Animals

Loss of stereopsis following lesions of cortical areas 17-18 in the cat.

The effects of bilateral removal of cortical areas 17-18 were investigated in the cat; these areas represent the central portion of the visual field and the effect of their removal was evaluated with reference to the perception of Julesz random-dot stereograms. Animals were trained in a two-choice discrimination box to choose between two stereotargets made out of random dots. When appropriately viewed, one produced a vertical rectangle and the other an horizontal one, which appeared to float out in space (crossed stereopsis). The results indicated that all normal cats could solve the random-dot task. Following the cortical lesions, stereoscopic perception was abolished. We also tested for the possibility that this inability to solve the random-dot problem was due to a more general acuity loss. Vernier-type acuity comparing a continuous to a disjointed line showed this to be within the animals' discriminative ability. Offset acuity of the lines was better than that of the stereodot patterns. On the other hand, the ability to determine the preoperatively acquired brightness and pattern discriminations was preserved, although some retraining was necessary for the more difficult patterns. It is therefore suggested that the primary visual cortex, at least in the cat, is involved in the perception of global stereopsis independently of its implication in the discrimination of bidimensional patterns.

Animals

Stereopsis in the cat: behavioral demonstration and underlying mechanisms.

The neural substrates subserving stereopsis were investigated behaviorally and electrophysiologically in the cat. In one set of studies, we examined behaviorally the ability of normal cats to perceive depth on the sole basis of spatial disparity using random-dot stereograms. Results showed that the animals were able to carry out this discrimination. We then evaluated the contribution of the optic chiasm, the corpus callosum and the primary visual cortex to this function. Results indicated that: (1) chiasma transection drastically reduced the ability of the animals to solve the random-dot problem; (2) a callosal split had little or no effect on their ability to relearn the same discrimination; (3) a section of both the corpus callosum and optic chiasm abolished this ability; and (4) bilateral lesions of areas 17-18 also abolished it. In another set of studies, we examined electrophysiologically the properties of neurons in the various visual cortical areas where disparity-based depth discrimination processes are presumed to take place. We recorded from areas 17, 18 and 19 of normal and split-chiasm cats. Results showed that: (1) the primary visual cortex of the normal cat contained cells sensitive to stimulus disparity; (2) these disparity sensitive neurons were also present in area 19 although in a much lower proportion and were more widely tuned than those in areas 17-18; and (3) following the section of the optic chiasm, there was a significant decrease in the number of disparity sensitive cells in areas 17-18, whereas in area 19 they were nearly completely absent. The results obtained from the lesion studies and from the single unit recording experiments indicate that stereoscopic depth perception is highly dependent in the cat upon the integrity of the through-the-chiasm geniculo-striate pathway and its target primary visual cortex.

Animals

Target detection and movement discrimination in the blind field of hemispherectomized patients.

Four hemispherectomized patients were tested with a variety of tasks designed to investigate the extent of residual vision in the blind field. The first set of studies was aimed at evaluating the ability of these subjects to detect and localize at various eccentricities three types of targets which differed in their spatiotemporal properties (stationary, flashing and moving). The subjects could detect effectively the presence of any of these stimuli in their blind field and they experienced little difficulty in discerning blank from target trials. When manual pointing was used to measure localization quality, the hemianopes made more errors in their blind field but their accuracy, when detection was correct, was comparable with that observed in their intact visual field and in that of the control subjects. In the second set of experiments, the capacity of 3 of the subjects to detect in their blind field a moving grating, as well as to discriminate between relative grating velocities and directions in their blind field and in both fields simultaneously, was assessed. Two subjects could detect the movement in their blind field, although this was in part affected by stimulus velocity. When discrimination of relative velocities in the blind field and in both fields simultaneously was evaluated, individual differences were observed. However, all subjects showed some capacity to carry out the task. Finally, none of the experimental subjects was able to discriminate the relative directions of the moving gratings. The results are discussed in terms of collicular involvement to account for the residual vision observed in the blind field of hemispherectomized subjects.

Brain

Bilateral interaction in the second somatosensory area (SII) of the cat and contribution of the corpus callosum.

There are indications in the literature that convergent ipsilateral and contralateral input to the second somatosensory area (SII) may interact. Single unit activity of SII bilateral cells was studied to evaluate the impact of simultaneous bilateral stimulation of the receptive fields (RF) on neural discharge. The cellular responses to unilateral ipsilateral and contralateral, as well as to bilateral stimulation were compared. 22% of bilateral cells showed interaction, usually facilitation. Bilaterally evoked responses were found to be as great as 250% of the strongest unilateral response. Only bilateral responses stronger or weaker than the dominant unilateral response by at least 50% were considered as interactive. The great majority of interactive cells had their RF on the forelimb and were responsive to deep stimulation. The corpus callosum appears to be responsible for part of the observed interaction since in callosotomized cats only 5% of bilateral cells were interactive. A non-callosal ipsilateral pathway must be postulated because both bilaterality and bilateral interaction persist to some degree after callosotomy. A putative role for bilateral interaction in sensory-motor integration is discussed.

Animals

Maturation of short latency somatosensory evoked potentials by median nerve stimulation: a cross-sectional study in a large group of children.

We have conducted two studies to evaluate the maturational changes of SEP in 206 subjects from neonatal period through adulthood. The first study was done with a cephalic reference electrode and included 137 subjects from 41 weeks (conceptional age) to 9 years of age, divided in 5 different age groups. In the second study, we used an extracephalic reference electrode and recorded SEPs in 69 normal subjects aged from 4 to 34 years, divided in 3 age groups. Our results show that there is a highly significant correlation between age and height in all the age groups studied. Peripheral and central components of SEP mature at different rates with adult values being reached for central conduction times (N9-P14, N9-N20, N13-N20 and P14-N20) between 4 and 9 years of age. Male and female subjects were compared in both studies and no significant differences were found in any of the age groups for any of the wave latencies or interpeak latencies analyzed.

Adolescent

[Plasticity of the callosal system].

A series of experiments examined the potential plasticity of the callosal system in both epileptic patients and in kittens submitted to corpus callosotomy at various ages. The patients were tested for unilateral discrimination and interhemispheric transfer of tactile information. The youngest patient was also required to perform additional inter- and intrahemispheric comparisons of visual and tactile stimuli. The animals were tested for interhemispheric transfer of visual discriminations. The results suggest that in both animals and humans there exists a critical period before which callosal section does not disrupt interhemispheric communication. The results also indicate that the compensatory mechanisms used to achieve interhemispheric transfer in the absence of the corpus callosum may vary according to the sensory modality involved. The possible physiological and/or functional mechanisms responsible for callosal plasticity are discussed.

Adolescent

Initial acquisition of visual discriminations following selective cortical lesions in cats.

Split-brain adult cats with various visual cortex lesions were tested for their ability to acquire several pattern discriminations using monocular vision. Different lesions were made in the two hemispheres to control for possible individual differences in learning speed due to factors other than the lesion. Results indicated that removal of either areas 17, 17 + 18, 18 + 19, or 19 did not abolish the ability to learn pattern discriminations. However, when compared to control animals, lesioned animals learned more slowly the various discriminations, especially subjects having lesions in 18 + 19. These results tend to confirm the hypothesis that the integrity of individual visual cortical areas for the perception and discrimination of simple patterns is important but not essential.

Animals

Receptive field properties of somatosensory callosal fibres in the monkey.

The corpus callosum is the principal neocortical commissure which transmits lateralized information between the hemispheres. The aim of the present experiment was to study the receptive field properties of somatosensory callosal fibres in rhesus macaque monkeys. The callosum was approached under direct visual control and axonic responses were recorded using tungsten microelectrodes. All sensory submodalities which could be examined with the available instruments were found (light touch, medium and deep pressure, joint movement and light pinches). Most fibres had receptive fields concerned with the trunk, followed by the head, with only a few responding to stimulation of the extremities. The medial borders of the unilateral receptive fields situated on the trunk and the head extended to the midline. The results are interpreted in terms of the roles of the corpus callosum in midline fusion and interhemispheric transfer.

Animals

Electrophysiological evidence for interhemispheric connections in the anterior ectosylvian sulcus in the cat.

We report electrophysiological data regarding the contribution of the corpus callosum to visual responses in the cortex around the anterior ectosylvian sulcus (AES). The experiments were performed in cats in which the optic input from each eye was surgically restricted to the ipsilateral hemisphere (split-chiasm cats), and where neuronal responses to stimulation of the contralateral eye were mediated by interhemispheric connections. A very high proportion of cells were driven by stimuli presented to either eye indicating that they were activated not only through an intrahemispheric pathway from the ipsilateral eye, but also through an interhemispheric pathway from the contralateral eye. With few exceptions, both receptive fields (RFs) of each binocular neuron abutted or were in the vicinity of the vertical meridian. All neurons responded well to moving stimuli and most of them showed directional selectivity. A few cells were activated by stimuli moving in depth. Following an additional section of the posterior half of the corpus callosum, cells in AES responded only to stimulation of the ipsilateral eye, demonstrating thus that the input from the contralateral eye was conveyed by this part of the corpus callosum. By contrast following a section of the anterior half of the corpus callosum, all visually responsive AES neurons were binocularly activated. These results suggest that the interhemispheric visual input to this ectosylvian region is conveyed via a polysynaptic loop involving visual cortical areas that are connected through the posterior portion of the corpus callosum.

Animals

Distribution of visual callosal projection neurons in the siamese cat: an HRP study.

In this experiment we studied the distribution of callosal cells in various visual cortical areas of both common and siamese cats using the HRP method. The results showed that the most notable difference between the two strains concerned the primary visual areas. Indeed, labeling in areas 17 and 18 was significantly lower in siamese cats and only a few scattered cells were encountered at the 17/18 border. In general, the number of callosal cells forming interhemispheric connections within areas 17, 18 and the 17/18 border was dramatically reduced in the siamese. For all other visual areas (19, lateral suprasylvian subdivisions, 20 a, b and 21 a, b) the distribution was comparable for both species. A study of the laminar distribution indicated that, for common and siamese cats, medium and large pyramidal cells were mainly concentrated in layers III and IV whereas in deeper layers we found a mixture of small pyramidal and fusiform neurons.

Animals

Stereoperception in cats following section of the corpus callosum and/or the optic chiasma.

The spatial separation of the eyes in animals with overlapping visual fields means that parts of a three dimensional object project to slightly disparate retinal points in each eye. This disparity, once interpreted by the brain, is thought to be a sufficient condition for stereoperception. In the present experiment, stereopsis based on spatial disparity cues was evaluated in cats using Julesz random-dot stereograms before and after sections of the optic chiasm, the corpus callosum or both. Normal cats were able to solve the random-dot problem. Optic chiasm transection drastically diminished this ability, callosal section had little effect and combined lesions of these two structures abolished stereoperception. These results suggest that central stereopsis based on spatial disparity is mainly mediated by binocular cortical cells receiving their input via the ipsilateral and the through-the-chiasm contralateral thalamo-cortical pathways.

Animals

Intracortical connections of the anterior ectosylvian and lateral suprasylvian visual areas in the cat.

Intra- and interhemispheric connections between the anterior ectosylvian visual area (AEV) and other visual cortical areas including the lateral suprasylvian (LSS) were examined in the cat using the retrograde double-label fluorescence technique. The areal and laminar distributions of labeled neurons were mapped following injections of different tracers: Evans Blue (EB), Fast Blue (FB) and Nuclear Yellow (NY) made separately into AEV and LSS of the same or opposite hemispheres. The results indicated: (1) reciprocal and bilateral AEV-LSS connections stemming from layers V and VI in addition to a predominant efferent LSS projection upon AEV from both layer III and the posterior lateral (PLLS) subdivision of LSS; (2) homotopic interhemispheric connections to AEV arising from layers III, V and VI and from layers III and V of ipsilateral areas 20 and 21a; (3) differential laminar distributions of the cell populations projecting to the two cortical sites injected including neurons in layer III of LSS which project to contralateral LSS and AEV of either hemisphere via collateral axon branching (double-labeled). The anatomical findings support the functional similarities between AEV and LSS and the possible role of AEV in interhemispheric transfer of visual information is discussed.

Animals

Harmaline-induced rhythmic activities of bulbar reticular cells and antagonistic muscles in the rat: a simultaneous recording study.

The harmaline-induced tremor of antagonistic muscles is studied in the anaesthetized rat. By recording simultaneously both the rhythmic EMG-activities in flexor and extensor muscles and the concomitant tremorogenic bulbar reticular discharges, we discovered two facts. 1) The extensor burst precedes the flexor muscle discharge by about 10 msec, contrarily to the close synchrony expected from anterior descriptions of harmaline tremor. 2) The previously observed periodical modulation of olivary and Purkinje cell rhythmic activities is transferred, through the reticular formation to the spinal level, in the form of an alteration of periods with tremor and periods with tonic coactivation of antagonistic muscles. The implication of the myotatic loop in the second fact is discussed.

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