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Biomedical subjects

A Berthoz

Publications and source records attributed to A Berthoz.

At least 109 records · Page 6Linked to original sources
PubMed1993

Saccadic eye movements and the horizontal vestibulo-ocular and vestibulo-collic reflexes in the intact guinea-pig.

The guinea-pig is an attractive model for investigating gaze stabilization because it is suitable for in vitro and in vivo studies. However, few data are available on its oculomotor performance. We therefore investigated spontaneous eye movements, horizontal vestibulo-ocular (HVOR) and vestibulo-collic reflexes (HVCR) in the alert head-fixed guinea-pig using the magnetic search coil method. First the characteristics of the spontaneous saccades in the light were analysed. They occurred with a mean frequency of 4.6/min and with a mean amplitude and duration of 7.41 +/- 3.57 deg and 30.9 +/- 9.5 ms, respectively (n = 340). Saccadic duration and velocity were linearly related to the amplitude of the eye movement. The HVOR was studied in response to sinusoidal rotations (0.01 Hz to 2 Hz, peak head velocity of 40 deg/s) in the dark. Vestibular responses were linear at 0.5 and 0.05 Hz for peak head velocities between 40 and 80 deg/s. As in other species, the gain increased and the phase lead decreased with increasing frequencies. The number of fast phases per second increased with peak head velocity and with increasing frequencies from 0.01 to 0.5 Hz, with a plateau between 0.2 and 0.5 Hz. The HVOR time constant, when measured in response to velocity steps, was 7.0 +/- 1.5 s and the latency of the vestibular responses averaged 21 +/- 4 ms. Finally, the HVCR was assessed in unrestrained guinea-pigs subjected to horizontal sinusoidal rotation in the frequency range of 0.05-2 Hz. Exploratory behaviour was prevalent and there were few head stabilization episodes.(ABSTRACT TRUNCATED AT 250 WORDS)

Animals↗
PubMed1993

The control of slow orienting eye movements by tectoreticulospinal neurons in the cat: behavior, discharge patterns and underlying connections.

The activity of tectoreticulospinal neurons (TRSN) during orienting gaze shifts was studied in alert, head-fixed cats by intra-axonal recordings. The scope of the study was to evaluate the role of this class of superior colliculus neurons in the generation of slow eye movements (drifts) which often follow main-sequence saccades and sometimes appear as an independent motor event of orienting. The parameters of such movements are described in the first part of the paper. The organization of underlying pathways in the lower brainstem has been studied by intra-axonal horseradish peroxidase (HRP) tracing. The mean amplitude of postsaccadic drifts (PSD) is 1.21 degrees (SD 0.63), but it can eventually reach 6-8 degrees. PSDs have mean velocity of 14.9 degrees/s (SD 4.28) and mean duration of 104.2 ms (SD 50.8). These two parameters are positively correlated with PSD amplitude. The presence of PSDs is usually associated with an increased neck muscle activity on the side toward which the eyes move. The durations of these two motor events show a reliable positive correlation. PSDs appear to occur when gaze error persists after a saccade and a correction is attempted by means of a slow eye movement and a head turn. The durations of TRSN bursts are, on average, longer than the sum of the lead time and the saccade duration. Bursts associated with combinations of saccades and PSD are significantly longer than those recorded in the absence of PSDs. The probability of occurrence of PSDs is higher when firing of TRSNs continues after saccade termination. Such prolonged discharges usually coincide with a combination of PSDs and phasic activation of the neck electromyogram. The mean firing rate of TRSNs during PSDs is 62% of that during saccade-related portions of the burst and declines to 45% after the end of PSDs. According to its timing and intensity, postsaccadic firing of TRSNs is appropriate as a signal underlying slow, corrective eye movements and later portions of phasic neck muscle contractions during orienting. Intra-axonal HRP labeling showed that visuomotor TRSNs of the X type (n = 3) terminate in the abducens nucleus, with 145-331 boutons terminaux and en passant. Average bouton densities in the nucleus are lower than in the periabducens reticular formation, but higher than in more rostral paramedian pontine reticular formation (PPRF) regions. Terminal fields in the PPRF match the locations of "eye-neck' reticulospinal neurons (RSNs) and exitatory burst neurons.(ABSTRACT TRUNCATED AT 400 WORDS)

Abducens Nerve↗
PubMed1993

Role of the different frontal lobe areas in the control of the horizontal component of memory-guided saccades in man.

Two paradigms of memory-guided saccades were studied in 14 patients with focal vascular lesions affecting either the frontal eye field (FEF), or the supplementary eye field (SEF) or Brodmann's area 46 in the prefrontal cortex (PFC), and in 13 age-matched control subjects. In the first paradigm, the subject had to remember the position of a visual target with the body immobile and, in the second, the position towards which gaze was directed before a body rotation, i.e. with a vestibular input. In control subjects, the percentage of error in saccade accuracy (horizontal component) was greater in the second than in the first paradigm (37% and 14% on average, respectively). Compared with controls, amplitude error was significantly increased in the FEF group for the first paradigm only, in the SEF group for the second paradigm only, and in the PFC group for both paradigms. These results are consistent with (1) the PFC providing an improvement in the utilization by the saccade system of the visual and vestibular signals used in the two paradigms, and (2) the FEF and SEF providing an improvement in the utilization of visual signals in the first paradigm and vestibular signals in the second paradigm, respectively. Furthermore, from these findings and experimental data, it may be hypothesized (1) that the PFC is a part of the network contributing to short-term memorization of both visual and vestibular signals, and (2) that the FEF and SEF control two different types of memory-guided saccades, with separate calculation modes to determine their amplitude.

Brain Mapping↗
PubMed1993

Effects of prolonged weightlessness on horizontal and vertical optokinetic nystagmus and optokinetic after-nystagmus in humans.

Horizontal and vertical optokinetic nystagmus (OKN) and optokinetic after-nystagmus (OKAN) provided by a partial-field, binocular optokinetic stimulator were recorded in one astronaut before, during, and after a 25-day space flight. A ground-based study was performed on six control subjects. During the flight experiment, performed on flight days 5, 18, 19, and 21, the subject either had their feet attached to the deck or was free-floating. Vertical OKN gain only slightly increased in weightlessness compared with ground data, but the center of interest (CI) during vertical OKN, evaluated by the eye position in the saggital plane at the end of the fast phases relative to the straight-ahead direction, was found to be significantly changed during long-term exposure to weightlessness. The horizontal CI showed very little change in-flight, but the gain was increased. The time constant for the astronaut was small for vertical OKAN, but there was an increase in slow-phase velocity (SPV) by the end of the flight, which returned to normal postflight. These results partly confirm the data obtained during head-tilt studies on the ground and are in accordance with the hypothesis of a gravity-dependent control of vertical gaze direction during orientation reflexes.

Acclimatization↗
PubMed1993

Effects of prolonged weightlessness on mental rotation of three-dimensional objects.

Previous experiments have suggested that the analysis of visual images could be a gravity-dependent process. We investigated this hypothesis using a mental rotation paradigm with pictures of three-dimensional objects during a 26-day orbital flight aboard the Soviet MIR station. The analysis of cosmonauts' response times showed that the mental rotation task is not greatly impaired in weightlessness. On the contrary, there are indications of a facilitation as: (1) the average rotation time per degree was shorter inflight than on the ground; (2) this difference seemed to be particularly marked for stimuli calling for roll axis rotations. However several factors may be responsible for this difference which was not obvious in one subject. Further experiments will have to test if this effect is really due to exposure to microgravity.

Adult↗
PubMed1993

Neural control.

Explore the source record for details and available documents.

Animals↗
PubMed1993

Saccade-vestibulo-ocular reflex co-operation and eye-head uncoupling during orientation to flashed target.

1. Eye-head co-ordination in the horizontal plane was studied in four human subjects using two successive flashes in the same direction, either increasing in eccentricity (IE), or decreasing in eccentricity (DE). 2. Results showed that for both conditions, head movements preceded eye movements and were typically longer or followed by a slow gaze movement. This slow movement was due to a vestibulo-ocular reflex gain of less than one. Gaze accuracy was achieved by small head movement adjustments. 3. Gaze movement to an IE stimulus had a staircase pattern, and to a DE stimulus, a pulse-step pattern or one gaze saccade to the final flash eccentricity. 4. In some cases, however, in response to a DE stimulus, the eye and head movements were directed to different displacements (dissociation); i.e. the head movement started towards the first flash eccentricity with a concomitant eye saccade to the second flash eccentricity. When this occurred, gaze movement did not resemble a pulse-step pattern. 5. It is suggested that non-visually orienting gaze is driven mainly by head movement. Eye and head movements can be either tightly coupled or dissociated, depending on the stimulus pattern.

Eye Movements↗
PubMed1993

PET study of voluntary saccadic eye movements in humans: basal ganglia-thalamocortical system and cingulate cortex involvement.

1. The purpose of this work was to explore the cortical and subcortical mechanisms underlying the execution of voluntary saccadic eye movements in humans. 2. Normalized regional cerebral blood flow (NrCBF) was measured using positron emission tomography (PET) and H2(15O) bolus intravenous injections in four right-handed healthy volunteers at rest and while performing self-paced voluntary horizontal saccadic eye movements in total darkness. 3. Magnetic resonance imaging of each subject's brain was matched to PET images, allowing the detection of activation in individually defined anatomic regions of interest. Cortical regions were drawn according to gyri limits; subcortical structures were also defined. 4. Self-paced saccadic eye movements elicited bilateral NrCBF increases in the lenticular nuclei, including putamen and globus pallidus, and in the thalamus. At the cortical level, we found bilateral NrCBF increases in the precentral gyrus, the superior part of the median frontal gyrus that corresponds to the supplementary motor area. There was also a significant NrCBF increase in the cerebellar vermis. 5. Right fusiform and lingual gyri, right insula, and left cingulate gyrus were also activated during the execution of saccades. 6. These results indicate that the classical basal ganglia-thalamocortical motor loop previously described for skeletal movements may also be involved in simple saccadic eye movements in humans.

Adult↗
PubMed1993

Estimation of passive horizontal linear whole-body displacement in humans.

1. Passive linear self-motion estimation along the X and Y axes was investigated in human subjects. 2. A target was viewed from a distance of 0.8 or 2.4 m from the starting point. Subjects were then blindfolded and transported toward the target on a distance of 3.2 m and back to the start. Acceleration was constant: +/- 0.2 or +/- 1 m/s2. The subjects pushed a button on both outward and return paths, when they passed the previously seen target. 3. The results showed anticipation of the target on the outward path, and not on the return. This was identical for both axes and both accelerations. 4. The data are in accord with a model of double integration of the otolith signal, suggesting that linear path integration is a basic sensory mechanism.

Acceleration↗
PubMed1993

Gaze control in microgravity. 1. Saccades, pursuit, eye-head coordination.

During the long-duration spaceflight Aragatz on board the Mir station, an experiment exploring the different oculomotor subsystems involved in gaze control during orientation to a fixed target or when tracking a moving target was executed by two cosmonauts. Gaze orientation: with head fixed, the "main sequence" relationships of primary horizontal saccades were modified, peak velocity was higher and saccade duration was shorter in flight than on earth, latency was decreased and saccade accuracy was better in flight. With head free, gaze orientation toward the target was achieved by coordinated eye and head movements, their timing was maintained in the horizontal plane; when gaze was stabilized on the target, there was a trend of a larger eye than head contribution not seen in preflight tests. Pursuit: Horizontal pursuit at 0.25 and 0.5 Hz frequency remained smooth with a 0.98 gain and minor phase lag, on earth and in flight. In the vertical plane, the eye did not track the target with a pure smooth pursuit eye movement, but the saccadic system contributed to gaze control. Upward tracking was mainly achieved with a succession of saccades, whereas downward tracking was due to combined smooth pursuit and catch-up saccades. This asymmetry was maintained during flight in head fixed and head free situations. On earth, head peak velocity was maximal upward, and in flight it was maximal downward.

Electrooculography↗
PubMed1993

Gaze control in microgravity. 2. Sequences of saccades toward memorized visual targets.

The reproduction, in complete darkness, of sequences of 5 horizontal saccades towards previously presented visual targets has been investigated in human subjects on the ground (control subjects) and one cosmonaut in microgravity. The incidence of corrective saccades during the execution of the memory-guided saccades in darkness has been examined. It was quite large for the control subjects (more than half of all saccades), and increased during the flight, while the corrective visually guided saccades incidence decreased. Direction errors occurred in about the third of all sequences on the ground, and this parameter also increased in microgravity. Memory-guided sequences were mostly hypermetric. Whereas the absolute error continuously increased with the target rank, it was not the case with the amplitude ratio, which presented a peak at the third rank, that is, at the middle of the sequence. The accuracy of the reproduction of the sequences did depend on the sequence pattern as much as on the subject. Some learning was observed in repeated reproduction of the same pattern. Although the average error did not change in microgravity, the linear regression coefficient between the visually guided and memory-guided saccades decreased.

Adult↗
PubMed1992

Effect of post-training unilateral labyrinthectomy in a spatial orientation task by guinea pigs.

The effects of unilateral labyrinthectomy in guinea pigs have been studied on an angular orientation task consisting, in an open field, of running to a hidden goal oriented at 45 degrees with respect to the cephalocaudal axis of the animal placed in a starting-box. The task was conducted in light but in an homogeneous environment, i.e. without visual, auditory or olfactory cues indicating the location of the goal. A second group of animals was submitted to a similar task running to a hidden goal but the place of the goal was indicated by a colored card. All the animals were trained before the lesion and tested in their respective task for 1 month after the lesion. In the task conducted without conspicuous cues, animals were dramatically disturbed. In contrast, animals pretrained in the visually guided task were not impaired after the lesion. These results point out the important role of vestibular information in performing spatial tasks based on angular estimation, since, even if proprioceptive and visuokinesthetic information remain available, subjects seemed not able to maintain a correct angular trajectory. The trajectories being not disturbed in the visually guided task, one can exclude the hypothesis that such deficit was due to a purely motor disturbance.

Animals↗
PubMed1991

A neural network model of sensoritopic maps with predictive short-term memory properties.

Coordinated orienting movements can be accurately performed without direct sensory control. Ocular saccades, for instance, have been shown to be reprogrammed after target disappearance when an intervening eye movement is electrically triggered before the saccade onset. Saccadic eye movements can also be executed toward memorized targets, even when the subject has been passively moved in darkness. Two hypotheses have been proposed to account for this goal-invariance property: either (i) the goal is reconstructed and memorized in the stable frame of reference linked to the environment ("allocentric, coordinates") or (ii) the goal is selected and memorized in the sensors-related maps ("egocentric coordinates") and is continuously updated by efferent copies of the motor commands. In this paper, we shall describe a formal neural network based on this second hypothesis. The results of the simulation show that target position can be memorized and accurately updated in a topologically ordered map, using a velocity-signal feedback. Moreover, this network has been submitted to a simple learning procedure by using the intermittent visual recurring afferent signal as the teaching signal. A similar mechanism could be involved in control of limb movement.

Computer Simulation↗
PubMed1991

Eye and head coupled and dissociated movements during orientation to a double step visual target displacement.

Tight coupling between eye and head movements has been observed in response to a single visual target offset. On this basis, when the visual stimulus consists of two successive steps in the same (horizontal) direction, either increasing in eccentricity (staircase) or decreasing in eccentricity (pulse-step) gaze should be due to concomitant eye and head angular displacement. That is, the eyes and head should aim at each target displacement so that their combined movement matches target offset. We have tested this hypothesis in five healthy subjects. The measured variables were head and gaze offset, the interval between two consecutive saccades from onset to onset (I) and the response delay between onset of the second step and onset of the first gaze saccade (D). With both staircase and pulse-step stimuli, the eye saccade preceded the head movement, and the gaze response either had the stimulus profile pattern or consisted of one gaze saccade to the final target offset. In response to staircase stimuli, I decreased concomitantly with an increase in D; with pulse-step stimuli, as D increased, I decreased slightly in three subjects and decreased markedly in two subjects. Dissociation between the eye and head movements could clearly be demonstrated with pulse-step stimuli: the first gaze saccade to the target pulse displacement was accompanied by a head movement to the target step offset. We also observed cases in which the gaze saccade to the target step displacement was made simultaneously with the head movement to the target pulse offset. Our study extends previous observations in head fixed condition and illustrates that in the majority of cases, when the head is free and a visual pulse step stimulus is presented, both the saccadic and head systems have the ability to modify or cancel the initial neural command to move to the first target displacement. When this modification takes place in only one system, eye and head movements are dissociated.

Electrooculography↗
PubMed1991

Head stabilization during various locomotor tasks in humans. II. Patients with bilateral peripheral vestibular deficits.

This experiment, which extends a previous investigation (Pozzo et al. 1990), was undertaken to examine how head position is controlled during natural locomotor tasks in both normal subjects (N) and patients with bilateral vestibular deficits (V). 10 normals and 7 patients were asked to perform 4 locomotor tasks: free walking (W), walking in place (WIP), running in place (R) and hopping (H). Head and body movements were recorded with a video system which allowed a computed 3 dimensional reconstruction of selected points in the sagittal plane. In order to determine the respective contribution of visual and vestibular cues in the control of head angular position, the 2 groups of subjects were tested in the light and in darkness. In darkness, the amplitude and velocity of head rotation decreased for N subjects; these parameters increased for V subjects, especially during R and H. In darkness, compared to the light condition, the mean position of a line placed on the Frankfort plane (about 20-30 degrees below the horizontal semi-circular canal plane) was tilted downward in all conditions of movement, except during H, for N subjects. In contrast, this flexion of the head was not systematic in V subjects: the Frankfort plane could be located above or below earth horizontal. In V subjects, head rotation was not found to be compensatory for head translation and the power spectrum analysis shows that head angular displacements in the sagittal plane contain mainly low frequencies (about 0.3-0.8 Hz). The respective contribution of visual and vestibular cues in the control of the orientation and the stabilization of the head in space is discussed.

Adult↗
PubMed1991

Eye-head coupling in humans. II. Phasic components.

A tonic coupling between the horizontal component of eye position and dorsal neck muscle activity has been demonstrated in animals and humans. In addition, a transient saccade related coupling has been found in animals. In order to investigate such a phasic component of the eye-head synergy in humans, we have recorded the activity of isolated motor units in the splenius muscle during large horizontal eye movements in head fixed subjects. Eye movement recording was achieved by conventional binocular electro-oculography and the activity of the right splenius muscle was recorded with Bronks coaxial electrodes inserted manually at the C4-C5 intervertebral level. We found two main types of motor unit discharge patterns in the splenius (SPMU), the first type (type A, 14 SPMUs) shows a phasic modulation of firing rate during saccades with a triphasic profile composed of a pre-saccadic suppression, a per-saccadic burst and a post saccadic tonic discharge proportional to eye position. The second type (type B, 6 SPMUs) exhibits little, if any, modulation of firing rate with either fixation or saccades. These results suggest that eye-head coupling is present not only during the fixation period but also during saccades and that a phasic activity or suppression related to saccadic eye velocity is present in dorsal neck muscle EMG.

Adult↗
PubMed1991

Head stabilization during locomotion. Perturbations induced by vestibular disorders.

Head kinematics was studied in 10 normal subjects (NS) and 7 patients (P) with bilateral vestibular deficit while they executed various locomotor tasks. The movement of the body was recorded with a video system which allowed a computer reconstruction of the motion of joint articulations and other selected points on the body in three dimensions. Analyses focus on head translation along the vertical axis and rotation in the sagittal plane. Two conditions were studied: free walking (W) and hopping (H). The subjects were tested in light and in darkness. In NS, while walking in darkness, mean head position was tilted downward. In contrast, this flexion was not systematic in P. Darkness did not significantly influence the amplitude and velocity of head angular displacement during W, but, during H the amplitude decreased by 37% for NS. During H in darkness, head stabilization decreased for P. These results suggest that head kinematics, during natural locomotor tasks, could be used to evaluate vestibular deficiencies.

Adult↗