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J R Duhamel

Publications and source records attributed to J R Duhamel.

17 recordsLinked to original sources
PubMed1996

The mental representation of hand movements after parietal cortex damage.

Recent neuroimagery findings showed that the patterns of cerebral activation during the mental rehearsal of a motor act are similar to those produced by its actual execution. This concurs with the notion that part of the distributed neural activity taking place during movement involves internal simulations, but it is not yet clear what specific contribution the different brain areas involved bring to this process. Here, patients with lesions restricted to the parietal cortex were found to be impaired selectively at predicting, through mental imagery, the time necessary to perform differentiated finger movements and visually guided pointing gestures, in comparison to normal individuals and to a patient with damage to the primary motor area. These results suggest that the parietal cortex is important for the ability to generate mental movement representations.

Adult↗
PubMed1996

Spatial representations for action in parietal cortex.

Parietal cortex contains multiple representations of visual space. Single neurons in area LIP encode attended locations relative to the fovea, while some VIP neurons encode stimulus location relative to the head and some MIP neurons may encode location relative to the arm. These multiple representations are tailored to guide specific kinds of actions: eye movements, head movements and arm movements, respectively. The function of parietal cortex is to signal the location of attended objects relative to the observer. It does so in order to allow the organism to act on its environment. The many different kinds of actions that can be performed are likely to be supported by these very different kinds of spatial representations.

Animals↗
PubMed1996

Visual, presaccadic, and cognitive activation of single neurons in monkey lateral intraparietal area.

1. Posterior parietal cortex contains neurons that are visually responsive and active in relation to saccadic eye movements. We recorded from single neurons in a subregion of parietal cortex, the lateral intraparietal area (LIP), in alert rhesus monkeys. To characterize more completely the circumstances under which LIP neurons are responsive, we used five tasks designed to test the impact of sensory, motor, and cognitive factors. We obtained quantitative data in multiple tasks in 91 neurons. We measured neural activity during central fixation and in relation to stimulus onset and saccade onset. 2. LIP neurons have visual responses to the onset of a stationary stimulus in the receptive field. These visual responses occurred both in tasks that require a subsequent eye movement toward the stimulus and in tasks in which eye movements are not permitted, indicating that this activity is sensory rather than presaccadic. 3. Visual responses were enhanced when the monkey had to use information provided by the stimulus to guide its behavior. The amplitude of the sensory response to a given stimulus was increased in a task in which the monkey would subsequently make a saccade to the location signaled by the stimulus, as compared with the amplitude of the visual response in a simple fixation task. 4. The visual response was also enhanced when the monkey attended to the stimulus without looking at it. This result shows that enhancement does not reflect saccade preparation because the response is enhanced even when the monkey is not permitted to make a saccade. Instead, enhancement reflects the allocation of attention to the spatial locus of the receptive field. 5. Many LIP neurons had saccade-related activity in addition to their visual responses. The visual response for most neurons was stronger than the saccade-related activation. 6. Saccade-related activity was independent of visual activity. Similar presaccadic activity was observed in trials that included a recent visual stimulus (memory-guided saccade task) and in trials with no visual stimulus (learned saccade task). 7. We observed increases in activity during fixation in tasks in which the monkey could anticipate the onset of a behaviorally significant stimulus. LIP neurons usually showed low levels of background firing in the fixation task during the period before stimulus onset. This background activity was increased in the peripheral attention and memory-guided saccade tasks during the period when the monkey was waiting for a behaviorally relevant stimulus to appear. 8. The results from these several tasks indicate that LIP neurons are activated in a variety of circumstances and are not involved exclusively in sensory processing or motor planning. The modulation of sensory responses by attention and anticipation suggests that cognitive factors play a major role in parietal function.

Animals↗
PubMed1995

Congruent unilateral impairments for real and imagined hand movements.

The chronometry of imagined and actual movements was investigated in a patient with a unilateral lesion of the motor cortex. Motor imagery generated highly accurate estimates of motor performance in a variety of situations, reflecting the hypokinesia of the contralesional hand. There were parallel increases in mental and actual movement times from proximal to distal limb segments. Bimanual movements adopted the slower speed of the impaired hand in both conditions. Imagined motor sequences to the beat of a metronome predicted the maximum speed reached in actual performance. Finally, visually guided pointing showed the same target-size effects in the imagery and movement conditions. The results are in agreement with the hypothesis that common cerebral motor representations are activated when imaging and planning voluntary movements.

Aged↗
PubMed1995

A selective impairment of hand posture for object utilization in apraxia.

This study reports the case of an apraxic patient who was impaired in all aspects of gestural behavior following bilateral posterior parietal cortex lesions. The main impairment concerned manual prehension of objects during their utilization. The deficit contrasted with both normal movement trajectories of the arm during execution of such gestures, and with accurate manual prehension in the context of simple reaching movements. Although recognition of gestures and pantomimes made by the examiner was preserved, the patient showed a striking inability to visually discriminate or describe manual prehension associated with object utilization. We thus propose the existence of specialized cortical mechanisms for the representation and activation of the postural schemata of the hand required for complex actions.

Apraxias↗
PubMed1993

Ventral intraparietal area of the macaque: anatomic location and visual response properties.

1. The middle temporal area (MT) projects to the intraparietal sulcus in the macaque monkey. We describe here a discrete area in the depths of the intraparietal sulcus containing neurons with response properties similar to those reported for area MT. We call this area the physiologically defined ventral intraparietal area, or VIP. In the present study we recorded from single neurons in VIP of alert monkeys and studied their visual and oculomotor response properties. 2. Area VIP has a high degree of selectivity for the direction of a moving stimulus. In our sample 72/88 (80%) neurons responded at least twice as well to a stimulus moving in the preferred direction compared with a stimulus moving in the null direction. The average response to stimuli moving in the preferred direction was 9.5 times as strong as the response to stimuli moving in the opposite direction, as compared with 10.9 times as strong for neurons in area MT. 3. Many neurons were also selective for speed of stimulus motion. Quantitative data from 25 neurons indicated that the distribution of preferred speeds ranged from 10 to 320 degrees/s. The degree of speed tuning was on average twice as broad as that reported for area MT. 4. Some neurons (22/41) were selective for the distance at which a stimulus was presented, preferring a stimulus of equivalent visual angle and luminance presented near (within 20 cm) or very near (within 5 cm) the face. These neurons maintained their preference for near stimuli when tested monocularly, suggesting that visual cues other than disparity can support this response. These neurons typically could not be driven by small spots presented on the tangent screen (at 57 cm). 5. Some VIP neurons responded best to a stimulus moving toward the animal. The absolute direction of visual motion was not as important for these cells as the trajectory of the stimulus: the best stimulus was one moving toward a particular point on the face from any direction. 6. VIP neurons were not active in relation to saccadic eye movements. Some neurons (10/17) were active during smooth pursuit of a small target. 7. The predominance of direction and speed selectivity in area VIP suggests that it, like other visual areas in the dorsal stream, may be involved in the analysis of visual motion.

Animals↗
PubMed1992

The updating of the representation of visual space in parietal cortex by intended eye movements.

Every eye movement produces a shift in the visual image on the retina. The receptive field, or retinal response area, of an individual visual neuron moves with the eyes so that after an eye movement it covers a new portion of visual space. For some parietal neurons, the location of the receptive field is shown to shift transiently before an eye movement. In addition, nearly all parietal neurons respond when an eye movement brings the site of a previously flashed stimulus into the receptive field. Parietal cortex both anticipates the retinal consequences of eye movements and updates the retinal coordinates of remembered stimuli to generate a continuously accurate representation of visual space.

Animals↗
PubMed1992

Saccadic dysmetria in a patient with a right frontoparietal lesion. The importance of corollary discharge for accurate spatial behaviour.

Double-step experiments have demonstrated that retinotopic coding is inadequate to explain the spatial performance of the saccadic system. In such experiments a subject is asked to make two successive saccades to fixate two sequentially flashed targets each of which disappears before the first saccade. Despite the dissonance thus created between the retinal location of the second target and the saccade necessary to acquire it, normal humans and monkeys perform the task perfectly well. Single unit recording in monkeys indicates that neurons in the superior colliculus, frontal eye fields and in parietal cortex generate a spatially accurate signal during the performance of double-step saccades, which is thought to be obtained by combining a retinotopic signal with a signal corollary to the previous saccadic eye movement. We studied saccadic eye movements in a patient with a right fronto-parietal lesion using single- and double-step tasks. Single saccades into the left (contralesional) hemifield had longer latency and were hypometric relative to those into the right (ipsilesional) hemifield. Varying the initial orbital position had no effect on the latency and accuracy of saccades to left and right retinal stimuli. When the patient was asked to do a double-step task with targets flashed first into the right field and then into the left field, she performed well. When she was asked to do the same task with a target flashed first into the left field and then into the right field she made the first saccade correctly but never acquired the second target, even though this required her to make a saccade in the normal direction to a stimulus that appeared in the normal field. Such a deficit therefore cannot be one of retinotopic or spatial coding, nor can it be one of generating a certain direction of saccade. We suggest that the deficit is a failure of corollary discharge, the inability to register the amplitude and direction of a saccade into the contralesional field, and use that information to update the representation of the location of the next saccade target.

Aged↗
PubMed1991

Heterogeneity of extrastriate visual areas and multiple parietal areas in the macaque monkey.

The definition of visual areas remains a key problem in the effort to elucidate cortical functions. Visual areas vary along a number of dimensions and are increasingly difficult to define according to traditional criteria at higher levels of the hierarchy. Three recently discovered areas in monkey parietal association cortex illustrate a new approach to this problem. Their definition depends on assessment of neuronal response properties in the alert, behaving animal combined with precise reconstruction of recording sites. This approach permits recognition of functionally distinct areas in the absence of retinotopic maps.

Animals↗
PubMed1991

The role of sensorimotor experience in object recognition. A case of multimodal agnosia.

Object recognition was studied in a 19-yr-old male patient who presented severe multimodal amnesia and agnosia without significant intellectual, linguistic or perceptual deficits. Bilateral temporal lobe lesions involved medial, polar and anterior infero-temporal structures. Although visual recognition was impaired to various extents for all categories of objects, preservation of certain capacities were demonstrated. In particular, the patient was able to determine specifically how to manipulate certain objects, in spite of his incapacity to define their function or their context of utilization. It is argued that object recognition involves different processing modes such that when direct access to representations of an object is impaired, sensorimotor information activated via alternative cortical and subcortical pathways may provide a limited mechanism for recognition.

Adult↗
PubMed1989

Audio-spatial deficits in humans: differential effects associated with left versus right hemisphere parietal damage.

In order to study auditory spatial localization in subjects with posterior damage involving the parietal lobe, we investigated their manual pointing performances to linguistic and white noise signals distributed over six sound sources situated in the anterior auditory field at ear level. The results showed: (1) A striking difference between patterns of deficits associated with right and left damage. In subjects with right damage, auditory localization deficits occurred in the horizontal plane, were manifested as restrictions in the peripheral left auditory hemifield and tended to be related to left visual neglect. In subjects with left damage, auditory localization deficits occurred in the entire auditory field in the horizontal as well as vertical planes, and they were particularly strong in the antero-frontal region. (2) One subject with right damage and visual neglect but no left auditory spatial restriction, showed deficits in the right hemifield where sound source location tended to be overestimated. This subject also showed a better discrimination of the origin of a white noise than of a linguistic signal. Results are discussed in terms of hemispheric asymmetries of function.

Acoustic Stimulation↗
PubMed1986

Deep dysphasia in a case of phonemic deafness: role of the right hemisphere in auditory language comprehension.

Deep dysphasia, an analogue of deep dyslexia in the auditory modality is a rare and peculiar pattern of repetition disturbance, which has been used to validate Morton's (Deep Dyslexia, pp. 189-196. Routledge & Kegan Paul, London, 1980) logogen theory. Such a case is reported here in which there was strong evidence of destruction of the left temporal lobe auditory areas. Examination of linguistic performance emphasized levels of auditory speech decoding. It was found that this patient had a profound phonemic discrimination deficit, yet could accomplish many lexical operations. It is argued that this case, in which a left temporal lobe lesion was associated with impaired phonological analysis, provides evidence that deep dysphasia may reflect the right hemisphere's non-phonological mode of speech processing.

Aphasia↗
PubMed1986

Manual pointing to auditory targets: performances of right versus left handed subjects.

In order to test the existence of an hemispheric asymmetry at a basic level of spatial information processing, six right handed and six left handed normal subjects were submitted to a manual pointing task to auditory targets. Results showed a shift in perceived target position according to the hand used for pointing, a striking asymmetry between the two auditory hemispaces reflected in both groups in directional error and dispersion.

Adult↗
PubMed1982

Effect of serotonin depletion induced by p-chloroamphetamine on changes in rats' activity levels-produced by lithium.

The role of serotonin (5-HT) transmission in the production of changes in rats' activity levels induced by 0.15 and 1.50 mEq/kg LiCl was assessed by selectively depleting 5-HT brain levels with p-chloroamphetamine prior to chronic administration of LiCl for 21 days. While p-chloroamphetamine pretreatment decreased 5-HT levels by 56%, irrespective of the fact that the animals had been administered either saline, 0.15, or 1.50 mEq/kg LiCl for 21 days, it did not alter the effects that each LiCl dose alone that on activity levels. Both LiCl administrations produced an 18% increase in 5-HT levels in rats pretreated with saline, yet diametrically opposed effects on activity levels. A parallel is drawn between these biochemical findings and previously reported data indicating that both LiCl doses produce an improvement in selective attention, yet opposed effects on rats' activity levels. The hypothesis that 5-HT transmission might be crucially involved in mediating the dose-independent effect of lithium on selective attention is proposed for future research.

Amphetamines↗
PubMedDate not supplied

Oculocentric spatial representation in parietal cortex.

Parietal cortex comprises several distinct areas. Neurons in each area are selective for particular stimulus dimensions and particular regions of space. The representation of space in a given area reflects a particular motor output by which a stimulus can be acquired. Neurons in the lateral intraparietal area (LIP) are active in relation to both visual and motor events. LIP neurons do not transmit an unambiguous saccadic command. Rather, they signal the location at which an event has occurred. These spatial locations are encoded in oculocentric coordinates, that is, with respect to the current or anticipated position of the center of gaze. When an eye movement brings the spatial location of a recently flashed stimulus into the receptive field of an LIP neuron, the neuron responds to the memory trace of that stimulus. This result indicates that, for nearly all LIP neurons, stored visual information is remapped in conjunction with saccades. Remapping of the memory trace maintains the alignment between the current image on the retina and the stored representation in cortex. Further, when an eye movement is about to occur, more than a third of LIP neurons transiently shift the location of their receptive fields. This anticipatory remapping allows the neuron to begin to respond to a visual stimulus even before the saccade is initiated that will bring the stimulus into the fixation-defined receptive field. Both kinds of remapping serve to create a constantly updated representation of stimulus location that is always in terms of distance and direction from the fovea. This oculocentric representation has the advantage that it already matches that known to exist in the frontal eye fields and the superior colliculus, the output targets of LIP, and it does not require further coordinate transformation in order to contribute to spatially accurate behavior. These results indicate that LIP can analyze visual space without ever forming a representation of absolute target position.

Animals↗