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Biomedical subjects

M Jeannerod

Publications and source records attributed to M Jeannerod.

At least 73 records · Page 4Linked to original sources
PubMed1991

Selective perturbation of visual input during prehension movements. 2. The effects of changing object size.

1. Subjects were instructed to reach and grasp cylindrical objects, using a precision grip. The objects were two concentric dowels made of translucent material placed at 35 cm from the subject. The inner ("small") dowel was 10 cm high and 1.5 cm in diameter. The outer ("large") dowel was 6 cm high and 6 cm in diameter. Prehension movements were monitored using a Selspot system. The displacement of a marker placed at the wrist level was used as an index for the transport of the hand at the location of the object. Markers placed at the tips of the thumb and the index finger were used for measuring the size of aperture of the finger grip. 2. Kinematics of transport and grasp components were computed from the filtered displacement signals. Movement time (MT), time to peak velocity (TPV) and time to peak deceleration (TPD) of the wrist, time to peak velocity of grip aperture (TGV), time to maximum grip aperture (TGA) were the main parameters used for comparing the movements in different conditions. Spatial paths of the wrist, thumb and index markers were reconstructed in two dimensions. Variability of the spatial paths over repeated trials was computed as the surface of the ellipses defined by X and Y standard deviations from the mean path. 3. Computer controlled illumination of one of the dowels was the signal for reaching toward that dowel. Blocks of trials were made to the small dowel and to the large dowel. Mean MT during blocked trials was 550 ms. The acceleration phase of the movements (measured by parameter TPV) represented 33% of MT. About half of MT (52%) was spent after TPD in a low velocity phase while the hand was approaching the object. This kinematic pattern was not influenced by whether movements were directed at small or large dowels. 4. Grip aperture progressively increased during transport of the hand. TGA corresponded to about 60% of MT, that is, maximum grip aperture was reached during the low velocity phase of transport. Following TGA, fingers closed around the object until contact was made. This pattern of grip formation differed whether the movement was directed at the large or the small dowel: TGA occurred often earlier for the small dowel, and the size of the maximum grip aperture was larger for the large dowel. Variability of both the wrist and finger spatial paths was larger during the first half of MT, and tended to become very low as the hand approached the dowels.(ABSTRACT TRUNCATED AT 400 WORDS)

Adult↗
PubMed1991

Temporal dissociation of motor responses and subjective awareness. A study in normal subjects.

The aim of the present study was to examine the timing of different responses given simultaneously to a single event, the sudden displacement of a visual object occurring at the onset of the grasping movement directed at that object. The subjects were requested to correct their movement in order to reach accurately for the object and to signal the time at which they became aware of its displacement by a simple vocal utterance (Tah!). The onset of the motor adjustment was measured using kinematic landmarks obtained from the hand trajectory. Movements executed during trials where the object was displaced had an earlier peak in acceleration (107 ms) than movements executed during control trials (120 ms). By contrast, the vocal signal occurred 420 ms following object displacement, that was more than 300 ms after the onset of the motor correction. Control experiments were performed in order to verify the influence of possible interferences between the two tasks. Motor corrections performed without vocal utterance had the same timing as when the vocal signal was produced. Vocal signals produced in response to object's displacements but in the absence of reaching movements had the same latency as when movements were performed. We conclude from these results that the two responses were generated independently of each other. Assuming that the vocal responses in this experiment did signal the subject's awareness, the observed delay between motor corrections and these responses suggests that neural activity must be processed during a significant and quantifiable amount of time before it can give rise to conscious experience. This dissociation between motor responses and awareness in normal subjects is discussed in the light of clinical cases where overt behaviour and conscious experience are dissociated by cerebral lesions.

Awareness↗
PubMed1991

Measuring time to awareness.

The timing of two simultaneous responses to one single visual event, namely the sudden subjective expansion of a real object occurring at the onset of a reaching movement, was measured in normal subjects. The motor response was represented by the earliest sign of correction in trajectory of the movement. The subjective report was represented by a vocal utterance that the subjects were instructed to emit when they became aware of the change in appearance of the object. The subjective report lagged the motor response by 150 ms. Control experiments ruled out a possible interference between the two responses. It is concluded that this temporal dissociation reflects a duality of neural pathways involved in processing object-related information.

Awareness↗
PubMed1990

The coupling of arm and finger movements during prehension.

The experiments reported here were aimed at testing the degree of coupling of motor components during the act of prehension. Hand movements were recorded bidimensionnally by a Selspot system which monitored the displacement of IREDS placed at the thumb and index finger tips, at the metacarpophalangeal joint of the index and at the radial styloid. Targets were three-dimensional translucent dowels placed concentrically at 30 cm from the subject. The dowels were 10 degrees apart from each other. In blocked and control trials, one dowel was illuminated and served as a target for the movement. In the perturbed trials (20% of cases) one dowel was illuminated first and the light was unexpectedly shifted to another dowel at the onset of the subject's movements. Kinematic analysis of the movement revealed the following: 1. In blocked and control trials, the wrist moved with a single acceleration to the target dowel. Meanwhile, the finger grip (computed as the distance between thumb and index IREDS) increased up to a maximum size, located in time at about 60% of movement time and then decreased until contact with the dowel. 2. In perturbed trials the initial wrist acceleration was aborted. A new acceleration started about 180 ms after the first, in order to reorient the hand to the new target. Similarly, the initial grip aperture also aborted and reincreased in synchrony with the second wrist acceleration. 3. Perturbations increased movement time by only 95 ms on average. The first peak in acceleration indicating abortion of the initial movement occurred 100 ms after the movement onset, i.e., 30 ms earlier than in non perturbed trials.(ABSTRACT TRUNCATED AT 250 WORDS)

Arm↗
PubMed1990

[Functional correlates of manual preference].

Manual preference develops early in life and does not become established until 5 years or more. Better performance of the preferred hand can be expressed in terms of higher spatial accuracy, lower kinematic variability and shorter latency of movements. These factors contribute to better ability of the preferred hand to rapidly produce alternated movements. Manual preference cannot be dissociated from hemispheric specialization, particularly for language functions. During normal motor activity, the 2 cerebral hemispheres (and the 2 hands) display complementary specialization.

Child↗
PubMed1989

The timing of mentally represented actions.

The performance of subjects walking blindly to previously inspected visual targets (located at 5, 10 or 15 m from the subjects) was studied in 2 experiments. In Expt. 1, subjects selected as good visual imagers were instructed to build up a mental representation of the target. Then they had to either actually walk or imagine themselves walking to the target. Walking time was measured in both the actual and the mental performance. It was found that subjects took almost exactly the same time in the two conditions. Accuracy of these subjects was also measured in the actual walking task. They were found to make no direction errors and to slightly overshoot target location. Subjects from another, control, group, who received no instructions about visual imagery made much larger errors. In Expt. 2, actual and mental walking times were measured in the same subjects as in Expt. 1, while they carried a 25-kg weight on their shoulders. In this condition, actual walking time was the same as in Expt. 1, although mental walking time was found to increase systematically by about 30%. These results are discussed in terms of the neural parameters encoded in the motor program for actually executing or mentally performing an action.

Adult↗
PubMed1989

[Egocentric reference and represented space].

The subjective estimate of the position of the egocentric reference was measured in normal right-handed subjects. They had to point manually in the straight ahead direction at what they thought was their body's sagittal plane. A systematic leftward bias of relatively small amplitude was observed for pointings with the right hand. No such bias was observed with the left hand. In addition, fixation of a visual target located within the right or left hemispace systematically deviated the estimated egocentric reference toward the side opposite to the target. These results contribute to the mechanisms responsible for directional coding of movements toward extrapersonal space.

Adult↗
PubMed1988

Neck muscle vibration modifies the representation of visual motion and direction in man.

The retinal coordinates of an image are normally insufficient to define the direction of an object in body-centred visual space. Gaze direction, specified by information on the position of eye-in-head and on the position of head-on-torso, is also required. While the source of the eye-in-head signal is controversial, it is clear that proprioceptive signals from neck muscles are sufficient to provide head-on-torso information. Observations by Goodwin et al., beginning in 1972, that vibration of limb muscles modifies proprioception from them, and induces illusory motion and false perception of limb position, suggested this study of the effects of neck muscle vibration on the representation of visual space. Verbal reports, supported by objective measures, revealed that vibration of muscles on one side of the neck induces a visual illusion: contralateral displacement of a small visual target viewed in the dark. Pointing movements towards the target are similarly affected, confirming that the representation of directions in visual space is modified by neck muscle vibration. A second vibration-induced illusion was uncovered when apparent displacement ceased. This is an illusion of pure target motion in the same direction as the previously observed displacement. The magnitudes of both the displacement and pure motion illusions were dependent on vibration amplitude and were unrelated to real or apparent movements of eyes or head. Taken together these observations indicate that vibration of neck muscles can modify independently (1) the central representation of the instantaneous direction of gaze and (2) the signal of the velocity with which this direction is changing.

Adult↗
PubMed1986

Visual control of reaching movements without vision of the limb. II. Evidence of fast unconscious processes correcting the trajectory of the hand to the final position of a double-step stimulus.

In this study, a visual target was localized by both limb and eye. The experimental procedure provided an opportunity to analyze the limb movement trajectories to the target whose location was displaced during saccades. Absence of visual information about position of the moving limb did not interfere with correction of the trajectory of pointing movements. These corrections reflect the new information about target position that becomes available at the end of the first saccade. Mean localization errors to stationary and to displaced targets were not significantly different. This result suggests that subjects were able to compare visual (retinal + eye position) information about the position of the target with information about the position of their moving limb derived from kinesthesis and/or efference copies of the motor commands. An analysis of velocity profiles indicates that the observed corrections of hand movement to target displacement could not be identified by an inflexion point in the trajectory. None of the subjects reported seeing the target change location. In other words, the motor command was adjustable despite the failure of changes in visual locus to reach consciousness.

Adult↗
PubMed1986

Mechanisms of visuomotor coordination: a study in normal and brain-damaged subjects.

This paper reviews the role of vision in controlling pointing and reaching movements in man. Studies of visuomotor behaviour in normal subjects allow the identification of several levels for describing organization of visuomotor control. The relative contribution of central (programming) and peripheral (feedback) mechanisms; the role of the eye-head coordinated position as a reference for controlling accuracy and direction of movements; and the relative independence of input-output channels in controlling proximal and distal segments of the musculature. These levels represent a useful framework for understanding pathological disruption of visuomotor control produced by cortical lesions.

Biophysical Phenomena↗
PubMed1986

The formation of finger grip during prehension. A cortically mediated visuomotor pattern.

The pattern of finger grip formation during natural prehension movements was described in normal subjects with the help of a quantified film technique. Movements were studied in one condition with visual feedback from the moving hand available, and one condition without visual feedback. The studied parameters, including the maximum size of the anticipatory grip and the final size of the grip before contact with the object, were not affected by shifting from one condition of visual feedback to the other. The same technique was applied to a group of patients with cerebral lesions. In two patients with unilateral lesions involving the motor cortex, grip formation with the hand contralateral to the lesion, was found to be severely affected, in that fingers and particularly the index finger, remained stretched until contact with the object was made. In two patients with unilateral lesions in the posterior parietal cortex, grip formation of the contralateral hand was absent specifically in the no-visual feedback condition. The same result was obtained in two other patients with a lesion (subcortical in one case, cortical in the other) of somatosensory pathways corresponding to one hand. These results are interpreted as evidence for the role of cerebral cortex in the control of finger grip formation during prehension of visual objects. Integration at cortical level of visual and somatosensory cues from the involved hand is a necessary condition for grip formation to be adapted to the grasp.

Adult↗
PubMed1986

[Vibration of neck muscles changes the apparent position of a visual target].

The discharge rate of muscle spindle afferents normally provides a precise signal of muscle length. Vibration of a muscle or its tendon induces an increase in afferent discharge which then no longer represents true muscle length; however, this increased proprioceptive input is interpreted in the central nervous system as a lengthening of the muscle. The incremented signal gives rise to illusions of displacement, or movement, of a fixed, vibrated limb. A visual target attached to such a vibrated limb also appears to move. We now report that vibration of the neck muscles influences visual localisation by inducing illusory movement of targets in visual space. Subjects were seated in a totally dark room and viewed a light-emitting diode (LED). The LED was placed at eye level approximately in the body midline at a distance of 70 cm. They held a physiotherapy vibrator in the left hand with its tip against the left side of the neck. When vibration was initiated the LED appeared to move rightward. The position of the tip of the vibrator was adjusted to produce the maximum apparent displacement to the right. In some subjects the illusion had a vertical component. Subjects maintained the vibrator in position and described the illusion when vibration began, during vibration and at its end. They reported that, initially, the target moved to the right but this displacement ceased after a second or two. The target then appeared to continue in motion without changing its position. When vibration ended the target returned to its initial position.(ABSTRACT TRUNCATED AT 250 WORDS)

Central Nervous System↗
PubMed1984

The contribution of coordinated eye and head movements in hand pointing accuracy.

The accuracy of pointing movements of the hand, directed at visual targets 10 degrees to 40 degrees from the midline, was measured in normal human subjects. No visual feedback from the moving hand was available to the subjects. The head could be either maintained stationary (head-fixed condition) or free to move (head-free condition) during the pointing movements. It was found that the error in pointing was reduced for all targets in the head-free condition. This reduction was more important for the more eccentric target (40 degrees). Improvement in accuracy was observed without any significant change in either the latency or the duration of eye, head or hand movements. In the head-free condition, it was found that the head was displaced in the direction of the target by an amount representing no more than 2/3 of the target amplitude. The improvement in accuracy was not influenced by the amplitude of the head movement. A model is proposed which shows how coordinated eye and head movements could improve the encoding of target position.

Adaptation, Physiological↗
PubMed1984

In search for the egocentric reference. A neurophysiological hypothesis.

Unilateral lesions of the middle suprasylvian gyrus in the cat parietal cortex produce an asymmetrical vestibulo-ocular reflex such that responses to head rotation toward the side opposite to the lesion become weaker. Unilateral lesions of the superior colliculus in the cat also produce the same effect. In either case symmetrical responses are recovered within 2-3 weeks. These results are discussed in terms of displacement, by the unilateral lesion, of an internal reference used for directing behaviour within extrapersonal space. Relevance of this hypothesis to clinical symptoms observed in man after unilateral posterior parietal lesions is discussed, with particular emphasis on the unilateral neglect phenomenon.

Animals↗