Jean-Paul Guillemot

Early- and Late-Onset Blind Individuals Show Supra-Normal Auditory Abilities in Far-Space

Blind individuals manifest remarkable abilities in navigating through space despite their lack of vision. They have previously been shown to perform normally or even supra-normally in tasks involving spatial hearing in near space, a region that, however, can be calibrated with sensory-motor feedback. Here we show that blind individuals not only properly map auditory space beyond their peri-personal environment but also demonstrate supra-normal performance when subtle acoustic cues for target location and distance must be used to carry out the task. Moreover, it is generally postulated that such abilities rest in part on cross-modal cortical reorganizations, particularly in the immature brain, where important synaptogenesis is still possible. Nonetheless, we show for the first time that even late-onset blind subjects develop above-normal spatial abilities, suggesting that significant compensation can occur in the adult.

Putting order into the development of sensitivity to global motion

We studied differences in the development of sensitivity to first-versus second-order global motion by comparing the motion coherence thresholds of 5-year-olds and adults tested at three speeds (1.5, 6, and 9 degrees s(-1)). We used Random Gabor Kinematograms (RGKs) formed with luminance-modulated (first-order) or contrast-modulated (second-order) concentric Gabor patterns with a sinusoidal spatial frequency of 3c deg(-1). To achieve equal visibility, modulation depth was set at 30% for first-order Gabors and at 100%, for second-order Gabors. Subjects were 24 adults and 24 5-year-olds. For both first- and second-order global motion, the motion coherence threshold of 5-year-olds was less mature for the slowest speed (1.5 degrees s(-1)) than for the two faster speeds (6 and 9 degrees s(-1)). In addition, at the slowest speed, the immaturity was greater for second-order than for first-order global motion. The findings suggest that the extrastriate mechanisms underlying the perception of global motion are different, at least in part, for first- versus second-order signals and for slower versus faster speeds. They also suggest that those separate mechanisms mature at different rates during middle childhood.

Sensory modality distribution in the anterior ectosylvian cortex (AEC) of cats

Modality specificity of neuronal responses to visual, somesthetic and auditory stimuli was investigated in the anterior ectosylvian cortex (AEC) of cats, using single-unit recording techniques. Seven classes of neurons were found, and according to their responsiveness to sensory stimuli regrouped into three categories: unimodal, bimodal and trimodal. Unimodal cells that responded to only one of the three stimulus modalities formed 59% of the units; 30.2% were bimodal, in that they showed a clear increase of neuronal discharges to two of the three stimulus types; 10.8% were defined as trimodal because they responded to all three stimulus modalities. Although the different categories of cells were intermingled within the AEC, indicating a certain degree of overlap between sensory modalities, some clustering of cell types was nonetheless evident. Thus, the somatosensory responsive cells were mainly located in the anterior two-thirds of the dorsal bank of the anterior ectosylvian sulcus. Visually responsive cells were concentrated on the ventral bank of the sulcus, whereas neurons with an auditory response occupied the banks and fundus of the posterior three-quarters of the sulcus. The histological distribution and physiological properties of AEC neurons suggest that this cortical region is a higher-order associative area whose function may be to integrate information from different sensory modalities.

Magnocellular and parvocellular developmental course in infants during the first year of life.

The visual system undergoes major modifications during the first year of life. We wanted to examine whether the magnocellular (M) and parvocellular (P) pathways mature at the same rate or if they follow a different developmental course. A previous study carried out in our laboratory had shown that the N1 and P1 components of pattern visual evoked potentials (PVEPs) were preferentially related to the activity of P and M pathways, respectively. In the present study, PVEPs were recorded at Oz in 33 infants aged between 0 and 52 weeks, in response to two spatial frequencies (0.5 and 2.5 c deg−1) presented at four contrast levels (4, 12, 28 and 95%). Results indicate that the P1 component appeared before the N1 component in the periods tested and was unambiguously present at birth. The P1 component showed a rapid gain in amplitude in the following months, to reach a ceiling around 4–6 months. Conversely, the N1 component always appeared later and then gained in amplitude until the end of the first year without reaching a plateau. Latencies were also computed but no developmental dissociation was revealed. Results obtained on amplitude are interpreted as demonstrating a developmental dissociation between the underlying M and P pathways, suggesting that the former is functional earlier and matures faster than the latter during the first year of life

Auditory responses in the visual cortex of neonatally enucleated rats.

A number of studies on humans and animals have demonstrated better auditory abilities in blind with respect to sighted subjects and have tried to define the mechanisms through which this compensation occurs. The aim of the present study, therefore, was to examine the participation of primary visual cortex (V1) to auditory processing in early enucleated rats. Here we show, using gaussian noise bursts, that about a third of the cells in V1 responded to auditory stimulation in blind rats and most of these (78%) had ON-type responses and low spontaneous activity. Moreover, they were distributed throughout visual cortex without any apparent tonotopic organization. Optimal frequencies determined using pure tones were rather high but comparable to those found in auditory cortex of blind and sighted rats. On the other hand, sensory thresholds determined at these frequencies were higher and bandwidths were wider in V1 of the blind animals. Blind and sighted rats were also stimulated for 60 min with gaussian noise, their brains removed and processed for c-Fos immunohistochemistry. Results revealed that c-Fos positive cells were not only present in auditory cortex of both groups of rats but there was a 10-fold increase in labeled cells in V1 and a fivefold increase in secondary visual cortex (V2) of early enucleated rats in comparisons to sighted ones. Also, the pattern of distribution of these labeled cells across layers suggests that the recruitment of V1 could originate at least in part through inputs arising from the thalamus. The ensemble of results appears to indicate that cross-modal compensation leading to improved performance in the blind depends on cell recruitment in V1 but probably also plastic changes in lower- and higher-order visual structures and possibly in the auditory system.

Sensory interactions in the anterior ectosylvian cortex of cats

Sensory interactions, namely, the responses of single cells to stimulations originating from the two sides of the body or from the two visual fields, or from more than one sensory modality (namely, visual, auditory and somatosensory), were evaluated within the anterior ectosylvian cortex (AEC) of cats. Results showed that responses of single neurons to a stimulus of one modality can be enhanced or inhibited by the presentation of another stimulus of either the same or another modality. This facilitatory or inhibitory modulation seems to depend upon temporal and/or spatial relationships between the stimuli. These results, taken together with those previously obtained in our laboratory and by others, suggest that neurons in the AEC may be involved in integrating inputs from various modalities and possibly linking sensory input with action.

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

SummaryBinocular 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.

Longer VEP latencies and slower reaction times to the onset of second-order motion than to the onset of first-order motion

We compared visual evoked potentials and psychophysical reaction times to the onset of first- and second-order motion. The stimuli consisted of luminance-modulated (first-order) and contrast-modulated (second-order) 1 cpd vertical sine-wave gratings drifting rightward for 140 ms at a velocity of 6 degrees /s. For each condition, we analysed the latencies and peak-to-baseline amplitudes of the P1 and N2 peaks recorded at Oz. For first-order motion, both P1 and N2 peaks were present at low (3%) contrast (i.e., depth modulations) whereas for second-order motion they appeared only at higher (25%) contrasts. When the two types of motion were equated for visibility, responses were slower for second-order motion than for first-order motion: about 44 ms slower for P1 latencies, 53 ms slower for N2 latencies, and 76 ms slower for reaction times. The longer VEP latencies for second-order motion support models that postulate additional processing steps for the extraction of second-order motion. The slower reaction time to the onset of second-order motion suggests that the longer neurophysiological analysis translates into slower detection.

Responses of cells to stationary and moving sound stimuli in the anterior ectosylvian cortex of cats.

The azimuthal, directional and angular speed sound selectivities of single units were examined in the posterior part of the anterior ectosylvian cortex. Broadband noise bursts and simulated moving sounds were delivered from 16 loudspeakers fixed on the horizontal plane in a quasi-anechoic sound-isolation chamber. The activity of 78 neurons was recorded and quantitatively analyzed. Most cells responded to at least the static sound. The relative strengths of their responses suggested that the cells could be classed as omnidirectional (37.2%), contralateral hemifield (29.5%), ipsilateral hemifield (2.5%) and azimuth (7.7%) selective. The remaining 23.1% could not be classified. All cells responded to a simulated moving sound displaced at five different speeds. A majority (88%) of them showed some directional preference in that they discharged at least twice as strongly for one direction as for the other for at least one speed. 14.7% displayed angular speed selectivity. Different patterns of neuronal discharges were evoked. For static sounds, most of the cells gave ON-type responses. A large proportion (60%) of the cells responded in a sustained manner to maintained stimulation. Among these, 68% also gave sustained discharges to moving sounds. The spatial tuning and the directional and angular speed selectivity of neurons in the posterior part of the AEC suggest that this area is involved in the processing of static and moving sounds.

Binocular interaction and disparity coding in area 19 of visual cortex in normal and split-chiasm cats

Binocular disparity, resulting from the projection of a three-dimensional object on the two spatially separated retinae, constitutes one of the principal cues for stereoscopic perception. The binocularity of cells in one hemisphere stems from two sources: (1) the ganglion cells in the homonymous temporal and nasal hemiretinae and (2) the contralateral hemisphere via the corpus callosum (CC). The objectives of this study were, on one hand, to determine whether disparity-sensitive cells are present in a “higher order” area, namely area 19 of the visual cortex, of the cat and, on the other hand, to ascertain whether the CC contributes to the formation of these cells. As in areas 17–18, two types of disparity-sensitive neurons were found: one type, showing maximal interactive effects around zero disparity, responded with strong excitation or inhibition when the stimuli presented independently to the two eyes 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 are presumed to signal stimuli situated in front of or behind the fixation plane. Unlike areas 17–18, however, disparity-sensitive cells in area 19 of the normal cat were less finely tuned and their proportion was lower. In the split-chiasm animal, very few cells were sensitive to disparity. These results, when coupled with behavioral data obtained with destriate animals, indicate that (1) area 19 is probably less involved in the analysis of disparity information than area 17, (2) the disparity-sensitive neurons that are sensitive to disparity are not involved in the resolution of very fine three-dimensional spatial detail, and (3) the CC only determines a limited number of these cells in the absence of normal binocular input.