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Eye movements evoked by proprioceptive stimulation along the body axis in humans.

Proprioceptive input arising from torsional body movements elicits small reflexive eye movements. The functional relevance of these eye movements is still unknown so far. We evaluated their slow components as a function of stimulus frequency and velocity. The horizontal eye movements of seven adult subjects were recorded using an infrared device, while horizontal rotations were applied at three segmental levels of the body [i.e., between head and shoulders (neck stimulus), shoulders and pelvis (trunk stimulus), and pelvis and feet (leg stimulus)]. The following results were obtained: (1) Sinusoidal leg stimulation evoked an eye response with the slow component in the direction of the movement of the feet, while the response to trunk and neck stimulation was oriented in the opposite direction (i.e., in that of the head). (2) In contrast, the gain behavior of all three responses was similar, with very low gain at mid- to high frequencies (tested up to 0.4 Hz) but increasing gain at low frequencies (down to 0.0125 Hz). We show that this gain behavior is mainly due to a gain nonlinearity for low angular velocities. (3) The responses were compatible with linear summation when an interaction series was tested in which the leg stimulus was combined with a vestibular stimulus. (4) There was good correspondence of the median gain curves when eye responses were compared with psychophysical responses (perceived body rotation in space; additionally recorded in the interaction series). However, correlation of gain values on a single-trial basis was poor. (5) During transient neck stimulation (smoothed position ramp), the neck response noticeably consisted of two components -- an initial head-directed eye shift (phasic component) followed by a shift in the opposite direction (compensatory tonic component). Both leg and neck responses can be described by one simple, dynamic model. In the model the proprioceptive input is fed into the gaze network via two pathways which differ in their dynamics and directional sign. The model simulates either leg or neck responses by selecting an appropriate weight for the gain of one of the pathways (phasic component). The interaction results can also be simulated when a vestibular path is added. This model has similarities to one we recently proposed for human self-motion perception and postural control. A major difference, though, is that the proprioceptive input to the gaze-stabilizing network is weak (restricted to low velocities), unlike that used for perception and postural control. We hold that the former undergoes involution during ontogenesis, as subjects depend on the functionally more appropriate vestibulo-ocular reflex. Yet, the weak proprioceptive eye responses that remain may have some functional relevance. Their tonic component tends to stabilize the eyes by slowly shifting them toward the primary head position relative to the body support. This applies solely to the earth-horizontal plane in which the vestibular signal has no static sensitivity.

Adult↗

What is deviant about deviant smooth pursuit eye movements in schizophrenia?

Smooth pursuit eye movements of schizophrenic, hospitalized nonpsychotic, and normal control subjects (18 per group) were measured in low and high target information conditions. A computer method for measuring saccade frequency and velocity was used. The results indicated that the frequency of saccades was significantly greater in both tracking conditions for schizophrenic than for hospitalized nonpsychotic or normal subjects. Consistent with our earlier finding, the reduction in saccade frequency with high information was greatest for schizophrenic subjects. The results also yielded a unique finding: the velocity of saccades within smooth pursuit records was significantly greater for schizophrenic than for hospitalized nonpsychotic or normal subjects. Greater saccade velocity was not a result of increased saccade size; there was no significant difference in the size of saccades for normal and schizophrenic subjects. Yet, the duration of saccades was significantly less for schizophrenics than for other subjects. Target information affected the frequency, duration and size, yet not the velocity of saccades emitted by all subjects. In contrast to earlier interpretations of deviant smooth pursuit eye movements in schizophrenia, the results may provide the first evidence of differences in the functioning of the saccadic eye movement systems of schizophrenic and normal subjects.

Adult↗

Eye movement control during reading: I. The location of initial eye fixations on words.

Sixty-six college students read two chapters from a contemporary novel while their eye movements were monitored. The eye movement data were analyzed to identify factors that influence the location of a reader's initial eye fixation on a word. When the data were partitioned according to the location of the prior fixation (i.e. launch site), the distribution of fixation locations on the word (i.e. landing site distribution) was highly constrained, normal in shape, and not influenced by word length. The locations of initial fixations on words can be accounted for on the basis of five principles of perceptuo-oculomotor control: a word-object has a specific functional target location, a saccadic range error occurs that produces a systematic deviation of landing sites from the functional target location, the saccadic range error is reduced somewhat for saccades that follow longer eye fixations, there exists perceptuo-oculomotor variability that is a second, nonsystematic source of variation in landing sites, and the perceptuo-oculomotor variability increases with distance of the launch site from the target.

Eye Movements↗

[Eye movement: from basic semiology to cognitive neuroscience].

Eye movements are an integral part of visual function. They are particularly well developed in frontal-eyed predator species. The abducens nuclei ensure lateral ocular motor synergy, while the oculomotor nuclei control vertical eye movements and convergence. The two main types of conjugate eye movement--saccades (image switching) and slow movements (image stabilization)--are controlled by specific brainstem premotor structures (respectively reticular and vestibular). Upstream of the brainstem, the cortical and subcortical pathways involved in eye movements are gradually being elucidated. Saccades are being used as a motor model to study the different cognitive processes, such as spatial memory, prediction and decision, involved in general movement preparation. The classical approaches based on lesion analysis, combined with transcranial magnetic stimulation and functional cerebral imaging, are contributing to our understanding of how the brain functions. Eye movements can be used for bedside diagnostic purposes, but also for sophisticated laboratory studies designed to explore the universe of cognition.

Animals↗

Predominance of nasal over temporal saccades in fast eye movement.

Quantitative analysis of saccadic eye movement caused by 20 degree amplitude gaze in horizontal plane was undertaken in 131 subjects using the Contraves' computerized oculomotor testing system. All of the subjects were free from any spontaneous nystagmus, neurological symptoms, and abnormalities of vestibular function. Both of the monocular recordings of saccade were made with a 3 sec time constant, 25 Hz high-cut filter, and digitized with a 3.9 msec sampling time. Four parameters i.e., maximum velocity, gain, latency, and duration, were analyzed. The average (S.D.) of each parameter was 337.1 (65.7) degree/sec, 1.00 (0.14), 199.1 (44.0) msec, and 128.3 (20.2) msec, respectively. We discussed the differences between nasal saccade and temporal saccade. The former was faster than the latter in maximum velocity and shorter in duration, while no differences were recognized in latency. It is suggested that the predominance of nasal saccade in fast eye movement is due to the anatomical difference of the vestibulo-ocular pathway between the medial rectus and the lateral rectus. In other words, because the synaptic inputs to the medial rectus are excitatory as opposed to the inhibitory and excitatory the inputs to the lateral rectus, the difference in muscle tone between the two muscles results in a faster maximum velocity of nasal saccades in fast eye movement.

Adult↗

Human anticipatory eye movements may reflect rhythmic central nervous activity.

To investigate the possibility that rhythmic activity originating in the central nervous system may modulate human eye movements, anticipatory eye movements were generated by tracking an intermittently obscured sinusoidally moving target. Eight subjects tracked intermittently obscured sinusoids of three different frequencies and of two different amplitudes. Eye movements were recorded by an infra-red reflection technique. The eye velocity records were analysed in the frequency domain by power spectral estimates. During periods where the target was obscured, eye movements consisted of a staggered series of anticipatory saccades with intervening smooth anticipatory eye movements or relatively stationary periods. In sections where the intervening smooth components of anticipatory tracking were of high velocity (above 15 deg/s), a superimposed smooth tremulous oscillation at around 10 Hz was sometimes present. Coherence analysis showed that this 10 Hz range oscillation of smooth anticipatory movement was not derived from head tremor and that the same oscillation was present in both eyes. This oscillation was not generally observed during smooth tracking of pseudorandom waveforms. Investigation of anticipatory eye movements has revealed a 10-Hz range oscillation or "tremor" superimposed upon smooth movements that might in other circumstances be inhibited by direct visual feedback. This smooth eye movement oscillation is thought to originate from the central nervous system and may reflect a widespread frequency modulation of motor commands.

Adult↗

Effects of gaze angle and extraretinal eye movement information on visual locomotion control.

This study tested effects of gaze--movement angle and extraretinal eye movement information on performance in a locomotion control task. Subjects hovered in a virtual scene to maintain position against optically simulated gusts. Gaze angle was manipulated by varying the simulated camera pitch orientation. Availability of extraretinal information was manipulated via simulated-pursuit fixation. In Experiment 1, subjects performed better when the camera faced a location on the ground than when it pointed toward the horizon. Experiment 2 tested whether this gain was influenced by availability of appropriate eye movements. Subjects performed slightly better when the camera pointed at nearby than at distant terrain, both in displays that did and in displays that did not simulate pursuit fixation. This suggested that subjects could perform the task using geometric image transformations, with or without appropriate eye movements. Experiment 3 tested more rigorously the relative importance of gaze angle and extraretinal information over a greater range of camera orientations; although subjects could use image transformations alone to control position adequately with a distant point of regard, they required eye movements for optimal performance when viewing nearby terrain.

Computer Simulation↗

Eye movements during transcendental meditation.

Characteristic changes in eye movements occurred during meditation with closed eyes in a proportion of subjects experienced in TM. The most common changes were an increase in slow, large-amplitude, 'rolling' eye movements and a concomitant decrease in rapid, low-amplitude, 'jerky' eye movements. Much variation occurred between individuals, however, some subjects showing no differences between TM and non-meditation. Any changes that occurred were not necessarily constant for the whole recording period nor consistent between sessions. The physiological effects of TM are far more variable than previously publicized. In general, the main changes in eye movements during TM are similar to those during passive hypnosis.

Adult↗

Eye movements in schizophrenia.

Smooth pursuit and other eye movements were quantitatively studied in patients with chronic schizophrenia to characterize the pattern and severity of eye movement abnormalities in this disorder. Twenty-one patients with schizophrenia, 13 patients with other psychiatric disorders (manic-depressive psychosis, schizoaffective disorder, depression and obsessive-compulsive disorder), and 19 normal subjects were studied. Horizontal eye movements were recorded with DC electro-oculography and analyzed by an online computer system. Eye velocity and closed-loop gain of pursuit, optokinetic nystagmus (OKN), vestibulo-ocular response (VOR) and visual-vestibular interactions were calculated. The latency, accuracy and peak velocity-amplitude relationships of voluntary saccades were measured. The group mean gains of pursuit and OKN of the schizophrenic patients were significantly lower than those of the normal subjects. Suppression of the VOR by fixation was impaired, and the latency of saccades was prolonged. However, the differences in group mean values were small in magnitude, and the frequencies of outliers among the schizophrenic patients were low. The patients with other psychiatric disorders had a similar pattern and severity of eye movement abnormalities. The frequency and severity of eye movement abnormalities in schizophrenic patients are lower than those indicated by previous studies that used different techniques of analysis.

Adolescent↗

Dynamics in longitudinal eye movements and corneal shape.

The magnitude and character of longitudinal movements of the eye were studied in the context of high speed videokeratoscopy. It was of interest to determine whether these dynamic changes in the eye movements can affect the corneal shape and its estimation. A high speed videokeratoscope with a sampling frequency of 50 Hz was used for measuring the corneal apex movements as well as for measuring variations in the best-fit sphere radius and central radius of curvature. The magnitude of the measured longitudinal apex movements could reach over 200 microm showing a slow trend. The estimated local changes of the apex movements that could be associated with the cardiopulmonary system were about 40-50 microm. The temporal variations in the equivalent estimated central radius of curvature ranged between 10 and 15 microm. Spectral analysis of the longitudinal eye movements revealed strong signatures of the pulse and respiration signals as well as the assumed blink control signal. No clear association between the longitudinal apex movements and the corneal curvature was found. However, very slow significant changes in the corneal shape were observed. The central radius of curvature of the cornea revealed slow changes of up to 120 microm. Understanding the nature of such changes will be of benefit in ophthalmic applications requiring highly accurate measurements of corneal shape, such as contact lens design and refractive surgery.

Cornea↗

The treatment of visual neglect using feedback of eye movements: a pilot study.

Feedback of eye movements was evaluated as a treatment for visual neglect in right hemisphere stroke patients. Patients with visual neglect identified on the Behavioural Inattention Test (BIT) were randomly allocated to two groups. One group (n = 9) was treated for 2 h 40 min a week for 4 weeks, by wearing glasses which provided a reminder bleep if patients failed to move their eyes to the left in a 15 s interval. The control group (n = 9) received no treatment for their visual inattention. Comparison of the groups after 4 weeks treatment and a further 4 weeks follow-up showed no significant difference either in eye movements or on the BIT. However, there was a trend towards a difference between eye movements in the two groups at 8 weeks, suggesting treatment may have influenced eye movements without changing neglect.

Aged↗

Does fatigue exist in a quantitative measurement of eye movements?

The measurement system for quantitative analysis of eye movements and distribution of eye fixation points was developed through the study. Experiments on physiological fatigue characteristics of eye movements were studied using the system. The subjects involved in the study were six young males. No significant change was quantitatively found in saccadic eye movements during and/or after five hours of rapid eye tracking tasks. The saccadic velocity of two subjects were found in binocular decreased temporarily. The maximum velocity of eye movements obtained in the present experiment was ascertained in order to produce a scale for various visual work as an ergonomic index.

Asthenopia↗

Initiation of sinusoidal tracking eye movements in man.

Smooth pursuit eye movement was recorded with a DC amplifier during horizontal sinusoidal target motion at 0.3, 0.6, 0.8, 1.0 and 1.2 Hz and a peak-to-peak amplitude of 20 degrees. Eye movement was digitalized at 100 Hz and 12 bits. From the digitalized eye movements, the maximum position error, the correlation coefficient and regression coefficients between stimulus and eye position were calculated in each half cycle. The A/D conversion and calculation were performed using a 16 bit microcomputer (NEC PC 98). Thirteen healthy volunteers with normal smooth pursuit patterns were examined. The correlation coefficient increased, but the maximum position error and the two regression coefficients decreased as the target moved. However, all four stabilized from about the 3rd half cycle regardless of the target frequency. These findings indicate that the smooth pursuit of a sinusoidally moving target reaches the maintenance at about the 3rd half cycle after initiation of two half cycles from the beginning of the target motion. This might be due to a prediction (or learning) of periodicity.

Adult↗

Some evidence for the hemispheric asymmetry model of lateral eye movements.

The relationship between lateral eye-movement patterns and visual spatial abilities was investigated for a sample of 94 right-handed junior high school boys and girls. Direction of gaze was recorded during reflection on a complex gross motor skill. Subjects were administered the Group Embedded Figures Test, the Kohs ' Block Design Test, the Hidden Figures Test, the Hidden Patterns Test, the Closure and Perceptual Speed Tests. Apart from the Group Embedded Figures Test and the Hidden Figures Test, low but significant positive relationships between proportion of left lateral eye-movements and visual spatial test scores were found. If lateral eye-movements are indicators of differential hemispheric activation, people with right-hemisphere predominance are more successful in solving certain visual-perceptual problems than people with left-hemisphere predominance. Finally, it is proposed that in studying relationships between lateral direction of eye-movements and field-dependence/independence, a more fruitful approach would be to investigate how people differ in their problem-solving styles to cope with embedded-figures test material in addition to determination of the performance level.

Adolescent↗

Introduction to the Symposium on Basic and Clinical Aspects of Vergence Eye Movements.

The basic aspects of vergence eye movements revolve about a central theme of a critique of the Maddox classification. Topics include interactions between accommodation and convergence in the absence of visual stimuli, dynamic properties of accommodative and fusional vergence, interactions between vergence eye movements and other visual motor systems, violations of Hering's law associated with specific components of vergence, and sources of fixation disparity. The clinical reports examine the effectiveness of disparate and accommodative stimuli for driving vergence eye movements in strabismus with normal or anomalous binocular correspondence. Effectiveness of dynamic and static tests of vergence eye movements is compared for detection of general binocular dysfunction. The Symposium is concluded with an open discussion of the basic and clinical reports.

Accommodation, Ocular↗

Changes in compartmental ventilation in association with eye movements during REM sleep.

The effect of phasic eye movement activity on ventilation during rapid-eye-movement (REM) sleep was studied in seven healthy young adults by use of the respiratory inductive plethysmograph. Mean ventilation (VE) and ventilatory components during REM sleep were not significantly different from that seen in either stages 1-2 or 3-4 sleep. The percent of rib cage contribution to ventilation in REM sleep, 29.3 +/- 5.1%, was reduced compared with 54.4 +/- 5.8% in stage 1-2 and 52.2 +/- 4.3% in stage 3-4 sleep (P less than 0.005). When one separated breaths by the degree of associated phasic eye movement activity, it became apparent that breathing during REM sleep is very heterogeneous. Increasing eye movement activity was associated with inhibition of ventilation with a reduction in VE from 5.1 +/- 0.3 to 3.8 +/- 0.3 l/min. Tidal volume and frequency both fell, whereas inspiratory duration was unchanged. Compartmental ventilation was also affected, with the fall in the rib cage contribution from 37.8 +/- 6.4 to 15.3 +/- 5.6%. Chest wall and abdominal movement became more asynchronous as phasic-eye-movement activity increased and frank paradoxical breathing was seen.

Adult↗

Impairment of smooth pursuit eye movement in chronic alcoholics.

Smooth pursuit eye movement was quantitatively evaluated in 99 chronic alcoholics and in 100 nonalcoholic control subjects. In both groups the smooth pursuit was increasingly impaired with advancing age, but in chronic alcoholics the smooth pursuit eye movement was more frequently (42.4%) impaired than in age-matched controls (20.0%, p less than 0.005). The characteristic feature of the impairment observed in chronic alcoholics was prominent saccadic movement of the eyes; ataxic pursuit was less common. It is suggested that the impairment of smooth pursuit eye movement in alcoholics is probably attributable to 'premature aging' of the cerebral cortex caused by chronic alcohol abuse.

Adult↗

[Clinical aspects of abnormal eye movements].

This paper reviews a variety of abnormal eye movements which include abnormal ocular positions, restricted eye motions, impairment of conjugated eye movements, abnormal smooth pursuit, abnormal saccade, gaze-evoked nystagmus, down-beat nystagmus, internuclear ophthalmoplegia, supranuclear ophthalmoplegia, square wave jerks, roving eye movement, ocular bobbing, ocular dipping, reverse ocular bobbing, and ping-pong gaze. Abnormal eye movements occur from stroke, spinocerebellar degeneration, Parkinson disease, multiple system atrophy, progressive supranuclear palsy, multiple sclerosis, Miller Fisher syndrome, myasthenia gravis, opsoclonus-polymyoclonia syndrome, and Creutzfeldt-Jakob disease. In neurological practice, it is important to observe abnormal eye movements accurately and enthusiastically, to make appropriate anatomical and etiological diagnosis.

Adult↗