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At least 469 records · Page 26Linked to original sources
PubMed2002

The relationship of fetal eye movements to non-stress test results.

OBJECTIVE: This study was designed to correlate ultrasound-observed fetal eye movements with fetal heart rate reactivity to determine its potential role in fetuses with persistent non-reactivity. METHODS: A total of 104 non-stress tests (NSTs) were evaluated in 62 patients referred for fetal surveillance for standard antepartum indications. Ultrasound-observed eye movements, assessed during portions of these NSTs, were categorized as negative (0), intermittent (1-5/min), or rapid (> or = 6/min). RESULTS: Of the NSTs, 97 were reactive and seven were non-reactive. All studied fetuses were apparently healthy, as the seven patients with persistently non-reactive NSTs had biophysical profile scores of 8/10. During the NSTs, 120 reactive portions and 81 non-reactive portions were evaluated for ultrasound-observed eye movements. During reactive portions, eye movements were negative 19% of the time, intermittent 24% of the time and rapid 56% of the time. During non-reactive portions, eye movements were negative 84% of the time, intermittent 7.8% of the time and rapid 7.8% of the time. All fetuses demonstrating eye movements during non-reactive periods became reactive shortly thereafter, and all of the seven persistently non-reactive fetuses displayed negative ultrasound-observed eye movements throughout the entire observation period. CONCLUSIONS: Healthy fetuses display a strong relationship between non-reactive heart rate tracings and absent or diminished eye movements, consistent with quiet sleep. Conversely, reactive periods are associated with a high incidence of rapid eye movement. Further study is needed in fetuses documented to be hypoxic.

Cardiotocography↗
PubMed2005

Inhibition of saccade and vergence eye movements in 3D space.

Inhibitory capacity was investigated by measuring the eye movements of normal subjects asked to fixate a central point, and to suppress eye movements toward visual distracters appearing in the periphery or in depth. Eight right-handed young adults performed such a suppression or distracter task. In different conditions, the distracter could appear at 10 degrees left or right at a distance of 20, 40, or 150 cm (calling for horizontal saccades), or in a central position far or close (calling for convergence or divergence), or 7.5 degrees up or down at 40 or 150 cm (calling for vertical saccades). Eye movements were recorded binocularly with an infrared light eye-movement device. Results showed that (1) suppression performance was not perfect, as the subjects still produced eye movements; (2) errors were distributed unequally in three-dimensional space, with more frequent errors toward distracters calling for convergence, or leftward and downward saccades at a close distance; (3) distracters calling for saccade suppression yielded saccades in the direction of the distracter (that we called prosaccades), and saccades directed away from it (that we called spontaneous antisaccades); (4) for vergence, only distracters calling for convergence yielded errors, which were always promovements; (5) in addition, a small convergent drift was found for convergence distracters. Differences in the errors between saccade and vergence suggest that different inhibitory mechanisms may be involved in the two systems. Spatial left/right, up/down, and close/far asymmetries are interpreted in terms of attentional biases.

Adult↗
PubMed2003

The disconnected brain stem does not support rapid eye movement sleep rebound following selective deprivation.

STUDY OBJECTIVES: To determine whether the brain stem can independently support the processes of rapid eye movement sleep rebound and pressure that follow deprivation. DESIGN: Cats with a brain-stem separation from the forebrain were compared to intact subjects on their response to rapid eye movement sleep deprivation. PARTICIPANTS: Eight adult mongrel cats of both sexes. INTERVENTIONS: All cats had electrodes implanted for polygraphic recordings, and 4 subjects sustained a mesencephalic transection. Weeks later, a 24-hour undisturbed sleep-wakefulness recording session was performed, and the next day, a similar session started with a 6-hour deprivation period, which was followed by 18 hours of undisturbed sleep. MEASUREMENTS AND RESULTS: Deprivation produced 90.1% and 87.8 % losses of rapid eye movement sleep time in intact and decerebrate cats, respectively. However, no significant changes in non-rapid eye movement sleep, drowsiness, or waking time percentages were seen in either group of animals when comparing the 6-hour time blocks of the deprivation and baseline sessions, indicating selective rapid eye movement sleep deprivation. During the 6-hour block following deprivation, rapid eye movement sleep time increased a significant 34.6% in intact cats while, in contrast, there was no rapid eye movement sleep rebound in decerebrate animals. The number of aborted episodes of rapid eye movement sleep during deprivation exceeded the number of episodes during the same period of the baseline day by 3 and 5 folds in intact and decerebrate cats, respectively, indicating an increase in rapid eye movement sleep pressure. CONCLUSIONS: Rebound in rapid eye movement sleep after deprivation cannot be sustained by the brain stem alone; in contrast, rapid eye movement sleep pressure persisted in the decerebrate cat, demonstrating that this process does not depend on descending forebrain influences. This indicates that rebound and pressure are 2 different components of the recovery process after rapid eye movement sleep deprivation and that, as such, are likely controlled by different mechanisms.

Animals↗
PubMed1980

Disorders of head and eye movements in children.

Disturbances of the normal relationship of head and eye movements occur in several pathological conditions, including disorders of rapid eye movements and various forms of congenital nystagmus. In disorders of rapid eye movements the abnormal head movements may be a learned response using various techniques to improve eye velocity and amplitude. In congenital nystagmus with head shaking, the head movements may be compensatory, of common genesis, or suppressive. The vestibulo-ocular reflex may be manipulated in certain circumstances to achieve eye stability or to increase eye movement velocity. In certain head tremors the eye movements observed may be normal vestibulo-ocular compensatory movements.

Apraxias↗
PubMed1993

Voluntary eye movement tests in patients with insulin-dependent diabetes mellitus.

Eye movement tests (saccade tests: reaction time, peak velocities and accuracy, and the eye tracking test) were studied in 53 insulin-dependent diabetic (IDDM) patients and 42 randomly selected non-diabetic control subjects, aged between 20 and 40 years. All subjects had central visual acuity of at least 0.1 in one eye, and none had ophthalmoplegia. The reaction time was longer and the accuracy decreased in the saccade test in diabetic patients as compared to control subjects. Peak velocities tended to be slower in diabetic patients, but no significant differences between diabetic and non-diabetic subjects were observed. The maximum eye movement velocities were reduced at all target velocities in diabetic patients as compared to control subjects. These findings can be explained on the basis of many potential disturbances in the central nervous system. Only the duration of diabetes had a clear association with maximum smooth pursuit eye movement velocities in the eye tracking test. Microvascular complications (retinopathy, nephropathy), autonomic neuropathy or metabolic control (high fasting blood glucose and glycated hemoglobin A1c) had no clear association with the results of eye movement tests. In conclusion, insulin dependent diabetes mellitus deteriorates the visuomotor responses.

Adult↗
PubMed1978

Frontal 'oculomotor" area in alert cat. I. Eye movements and neck activity evoked by stimulation.

(1) Stimulation within cat frontal lobe elicited saccadic eye movements whose maximum velocity was significantly greater than that of normal spontaneous saccades. (2) The majority (90%) of stimulated cortical points yielded eye movements whose directions and amplitudes were independent of the position of the eye in the orbit. The direction of these eye movements depended on the site being stimulated, with a discrete and orderly representation of directions existing within the cortex. (3) A lesser number of cortical points (10%) yielded centering movements whose directions and amplitudes depended on the position of the eye in the orbit, rather than on the site being stimulated. (4) Evoked neck muscle activation frequently preceded evoked eye movements by some 15--30 msec. This timing was compatible with a coordinated head-eye orientating response. (5) On the basis of the directions, and the latencies, of evoked eye movements, the cat frontal oculomotor area could be divided into two subregions, a 'medial' and a 'lateral', (6) The 'medial' area included the mesial wall of the hemisphere with a portion of the lower lip of the cruciate sulcus, and the medial wall of the presylvian sulcus. This area yielded contraversive eye movements with shorter latencies (average 45 msec). (7) The 'lateral' area included primarily the lateral wall of the presylvian sulcus. It yielded predominantly centering eye movements, and ipsiversive movements with longer latencies (65 msec). (8) The functional characteristics of the 'medial' area, as revealed by focal stimulation, resembled those of the monkey frontal eye field.

Animals↗
PubMed1976

The temporal and periodic organization of REM eye movements in mental retardation.

Time trends and periodic cycles in REM sleep eye movements were examined in 6 functional and 6 mongoloid adolescent retardates. Both groups of subjects showed approximately equal percentages of linear trends, quadratic trends, linear and quadratic trends, and absence of trend. The eye movement time-series were subject to an orthogonal spectral analysis. In both groups of subjects, peak spectral estimates generally occurred at 10.6- or 21.3-min periods. Following this, the eye movements of the longest REM periods (and one long period of pre-sleep wakefulness) were subject to a least-squares spectral analysis. This analysis yielded estimates ranging from 22 to 44 min. Eye movements lacked the ultradian organization previously reported for eye movements of normal subjects. These results imply that the ultradian organization of REM sleep and the ultradian organization of eye movements may be independent.

Adolescent↗
PubMed2000

Initiation of smooth-pursuit eye movements to first-order and second-order motion stimuli.

Since normal human subjects can perform smooth-pursuit eye movements only in the presence of a moving target, the occurrence of these eye movements represents an ideal behavioural probe to monitor the successful processing of visual motion. It has been shown previously that subjects can execute smooth-pursuit eye movements to targets defined by luminance and colour, the first-order stimulus attributes, as well as to targets defined by derived, second-order stimulus attributes such as contrast, flicker or motion. In contrast to these earlier experiments focusing on steady-state pursuit, the present study addressed the course of pre-saccadic pursuit initiation (less than 100 ms), as this early time period is thought to represent open-loop pursuit, i.e. the eye movements are exclusively driven by visual inputs proceeding the onset of the eye movement itself. Eye movements of five human subjects tracking first- and second-order motion stimuli had been measured. The analysis of the obtained eye traces revealed that smooth-pursuit eye movements could be initiated to first-order as well as second-order motion stimuli, even before the execution of the first initial saccade. In contrast to steady-state pursuit, the initiation of pursuit was not exclusively determined by the movement of the target, but rather due to an interaction between dominant first-order and less-weighted second-order motion components. Based on our results, two conclusions may be drawn: first and specific for initiation of smooth-pursuit eye movements, we present evidence supporting the notion that initiation of pursuit reflects integration of all available visual motion information. Second and more general, our results further support the hypothesis that the visual system consists of more than one mechanism for the extraction of first-order and second-order motion.

Adult↗
PubMed1992

An adjustment to eye movement measurements that compensates for the eccentric position of the eye relative to the center of the head.

We describe a procedure for modifying horizontal eye movement measurements in a way that effectively removes signal contributions due to the eccentric location of the eyes relative to the center of rotation of the head. This procedure helps standardize measured signals so that data collected under different experimental conditions and from different subjects may be compared directly. We also present techniques for accurately determining specific parameters of head geometry that are required by the procedure. This method may be used for modifying eye movement responses to visual target motion, head motion, or both, and does not assume continual fixation of the visual target. Also, this method may be employed when either curved (iso-distance) or flat display screens are used for presenting the visual stimuli.

Eye↗
PubMed1990

Eye movements in acute, chronic, and remitted schizophrenics.

Eye movements in 10 acute schizophrenics, 50 chronic schizophrenics, 20 remitted schizophrenics, 25 methamphetamine psychotics, 21 temporal lobe epileptics with left-sided spike focus (l-focus), 12 temporal lobe epileptics with right-sided spike focus (r-focus), and 50 normal controls were examined with an eye mark recorder while they viewed geometric figures. The eye movements while viewing an original "S"-shaped figure for 15 sec were analyzed. Each schizophrenic group and methamphetamine psychotics had significantly less eye fixations than the normal controls and temporal lobe epileptics (r-focus and l-focus). The chronic schizophrenics had significantly shorter mean eye scanning length (MESL) than the other six groups. Each subject was then shown two other figures slightly different from the original and was requested to compare them with the original. After comparing them, the subjects were asked the question, "Are there any other differences?" The 5-sec eye movements during the response to this question were scored using the Responsive Search Score (RSS). The schizophrenic groups had a significantly lower RSS than the nonschizophrenic patient groups and the normal controls. In the chronic schizophrenics, there was a significant negative correlation between the RSS and negative symptoms. These results suggest that the MESL can be an indicator of a chronic process of schizophrenia, and that lowering of the RSS may be a nosologically specific indicator for schizophrenia.

Acute Disease↗
PubMed1977

Lateral eye movements during verbal and nonverbal dichotic listening.

A dichotic listening paradigm was used to study the relation of eye movement to cerebral lateralization. The eye movements of right-handed subjects were recorded during verbal and nonverbal dichotic-listening tasks. Subjects given a verbal dichotic-listening task made significantly more rightward than leftward eye movements and showed more accuracy and speed in processing information presented to the right than to the left ear. Subjects given a nonverbal dichotic-listening task made significantly more leftward eye movements and processed better information presented to the left ear. These findings suggest a potentially strong link between the direction of lateral eye movement during dichotic listening tasks and left- and right-ear advantages in performance on such tasks. They also suggest that both eye movement and ear performance may be related to cerebral laterality and when examined in combination both could provide valuable information for the further study of hemispheric specialization.

Acoustic Stimulation↗
PubMed1984

Functional localization in the three floccular zones related to eye movement control in the cat.

Anatomically, the cat's cerebellar flocculus can be divided into 3 zones on the basis of differences in their efferent projection sites. The functional differences of these 3 zones in relation to eye movement control were investigated by observing the eye movements evoked by electric stimulation of each zone of the flocculus in ketamine-anesthetized cats. Stimulation of the flocculus elicited a slow eye movement. The direction of the slow eye movement was mapped. A downward eye movement was evoked by stimulation of the caudal zone. An ipsilateral horizontal eye movement was induced from the middle zone. An upward eye movement was elicited from the rostral zone. When prolonged stimulation was applied to the flocculus, the slow eye movement was followed by nystagmus in the opposite direction. This nystagmus persisted for many seconds after cessation of stimulation (afternystagmus). Nystagmus and afternystagmus could not be elicited in deeply anesthetized cats. Possibilities as to how the stimulation leads to various eye movements are discussed.

Animals↗
PubMed2002

Common inhibitory mechanism for saccades and smooth-pursuit eye movements.

The premotor pathways subserving saccades and smooth-pursuit eye movements are usually thought to be different. Indeed, saccade and smooth-pursuit eye movements have different dynamics and functions. In particular, a group of midline cells in the pons called omnipause neurons (OPNs) are considered to be part of the saccadic system only. It has been established that OPNs keep premotor neurons for saccades under constant inhibition during fixation periods. Saccades occur only when the activity of OPNs has completely stopped or paused. Accordingly, electrical stimulation in the region of OPNs inhibits premotor neurons and interrupts saccades. The premotor relay for smooth pursuit is thought to be organized differently and omnipause neurons are not supposed to be involved in smooth-pursuit eye movements. To investigate this supposition, OPNs were recorded during saccades and during smooth pursuit in the monkey (Macaca mulatta). Unexpectedly, we found that neuronal activity of OPNs decreased during smooth pursuit. The resulting activity reduction reached statistical significance in approximately 50% of OPNs recorded during pursuit of a target moving at 40 degrees /s. On average, activity was reduced by 34% but never completely stopped or paused. The onset of activity reduction coincided with the onset of smooth pursuit. The duration of activity reduction was correlated with pursuit duration and its intensity was correlated with eye velocity. Activity reduction was observed even in the absence of catch-up saccades that frequently occur during pursuit. Electrical microstimulation in the OPNs' area induced a strong deceleration of the eye during smooth pursuit. These results suggest that OPNs form an inhibitory mechanism that could control the time course of smooth pursuit. This inhibitory mechanism is part of the fixation system and is probably needed to avoid reflexive eye movements toward targets that are not purposefully selected. This study shows that saccades and smooth pursuit, although they are different kinds of eye movements, are controlled by the same inhibitory system.

Action Potentials↗
PubMed1997

Visual receptive fields of neurons in primary visual cortex (V1) move in space with the eye movements of fixation.

We tested the hypothesis that receptive field (RF) locations of visual cortex cells maintain a fixed location on the retina and move in space with movements of the eye. Responses to a bar swept across the RF were recorded from 29 neurons in V1 (26) and V2 (3) of alert monkeys while precisely monitoring the eye movements of fixation. There was a tight correlation and a near unity ratio between eye position and RF position. This implies that RFs of V1 neurons and at least some V2 neurons are fixed to specific retinal locations, rather than being shifted on the retina by attention-controlled mechanisms. V1 neurons thus differ from those polysensory neurons whose RF locations on the retina are dynamically altered to maintain a desired position in space.

Animals↗
PubMed2005

Smooth pursuit-like eye movements during mental extrapolation of motion: the facilitatory effect of drowsiness.

We studied eye movements during mental extrapolation of motion. Subjects tracked with the eyes a target oscillating sinusoidally by +/- 5 degrees on the horizontal plane at frequencies between 0.15 and 0.5 Hz. After 4 cycles the target disappeared and subjects had to mentally extrapolate its motion in imagery for 5 further cycles. Subjects were invited to relax. We recorded eye movements with infrared oculography and the lid aperture with a webcam. Typically, in the imagery phase, sequences of saccades "reproduced" the macroscopic characteristics of the to-be-imagined motion. However, slow eye movements substituting the sequence of saccades emerged repeatedly in the course of the experiment, to the extent that sometimes it was almost impossible to distinguish the pattern of eye movements during tracking from that during imagery. These smooth pursuit-like eye movements lasted up to 17 s, although they were more commonly intermingled with saccades. It turned out that this phenomenon occurred mostly, although not exclusively, when the lids were partially lowered suggesting an association with drowsiness. The average gain of smooth pursuit-like eye movements in imagery passed from 0.09 when the lids were open, to 0.27 when they were partially lowered. A control experiment excluded that the lowering of the lids per se had played any important role. This finding has implications for both the physiology of the oculomotor system and for the debate on the relation between imagery and perception.

Acoustic Stimulation↗
PubMed2004

Exogenous orienting of attention depends upon the ability to execute eye movements.

Shifts of attention can be made overtly by moving the eyes or covertly with attention being allocated to a region of space that does not correspond to the current direction of gaze. However, the precise relationship between eye movements and the covert orienting of attention remains controversial. The influential premotor theory proposes that the covert orienting of attention is produced by the programming of (unexecuted) eye movements and thus predicts a strong relationship between the ability to execute eye movements and the operation of spatial attention. Here, we demonstrate for the first time that impaired spatial attention is observed in an individual (AI) who is neurologically healthy but who cannot execute eye movements as a result of a congenital impairment in the elasticity of her eye muscles. This finding provides direct support for the role of the eye-movement system in the covert orienting of attention and suggests that whereas intact cortical structures may be necessary for normal attentional reflexes, they are not sufficient. The ability to move our eyes is essential for the development of normal patterns of spatial attention.

Adult↗
PubMedDate not supplied

Abnormal supranuclear eye movements in the child: a practical guide to examination and interpretation.

Abnormal eye movements in the infant or voting child can be congenital or acquired. They may be a result of abnormal early visual development or a sign of underlying neurologic or neuromuscular disease. It is important to be able to detect these abnormalities and to distinguish them from normal but immature eye movements. The spectrum of disease in children differs from that in adults. Serious, potentially fatal but treatable disorders can be acquired in infancy, and abnormal eye movements in a sometimes apparently well child should never be labeled as congenital or benign without careful investigation. Eye movement analysis can indicate the presence of an underlying condition and help the clinician to classify different neurologic diseases. It is important to carefully examine the ocular motor system in any children at risk of neurologic disease. This review provides a practical guide to the examination and interpretation of eye movements in the child and includes recent literature on eye movement disorders of childhood. We describe supranuclear abnormalities of the ocular motor system in the order in which we would normally examine it: saccades, pursuit, convergence, vestibulo-ocular reflex, and optokinetic nystagmus. Nystagmus, internuclear ophthalmoplegia, cranial nerve abnormalities, and "miswiring" phenomena (such as Duane's syndrome and synergistic divergence) are not discussed.

Child↗
PubMedDate not supplied

Effects of directional expectations on motion perception and pursuit eye movements.

Expectations about future motions can influence both perceptual judgements and pursuit eye movements. However, it is not known whether these two effects are due to shared processing, or to separate mechanisms with similar properties. We have addressed this question by providing subjects with prior information about the likely direction of motion in an upcoming random-dot motion display and measuring both the perceptual judgements and pursuit eye movements elicited by the stimulus. We quantified the subjects' responses by computing oculometric curves from their pursuit eye movements and psychometric curves from their perceptual decisions. Our results show that directional cues caused similar shifts in both the oculometric and psychometric curves toward the expected motion direction, with little change in the shapes of the curves. Prior information therefore biased the outcome of both eye movement and perceptual decisions without systematically changing their thresholds. We also found that eye movement and perceptual decisions tended to be the same on a trial-by-trial basis, at a higher frequency than would be expected by chance. Furthermore, the effects of prior information were evident during pursuit initiation, as well as during pursuit maintenance, indicating that prior information likely influenced the early processing of visual motion. We conclude that, in our experiments, expectations caused similar effects on both pursuit and perception by altering the activity of visual motion detectors that are read out by both the oculomotor and perceptual systems. Applying cognitive factors such as expectations at relatively early stages of visual processing could act to coordinate the metrics of eye movements with perceptual judgements.

Adult↗