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A comparison of predictive and nonpredictive ocular pursuit under active and passive stimulation conditions in humans.

A technique has been developed for the comparison of predictive and nonpredictive ocular pursuit in human subjects, with the objective of estimating the contribution made by predictive processes to the normal pursuit response. Subjects were presented with a target moving at constant velocity in the horizontal plane and instructed to actively pursue the target or to passively stare at it. In the predictive mode (PRD), a step-ramp stimulus with velocity ranging from 12.5 to 50 degrees/s was presented at regular intervals of 1.728 s, in alternating directions, with target exposure durations (PD) that varied from 80 to 640 ms. In the interval between presentations, subjects were in complete darkness. In the nonpredictive mode (RND), similar step-ramp stimuli were presented but with randomized direction and timing of target exposure. In the nonpredictive mode, during both active and passive stimulation, the smooth component of eye velocity was initiated after a mean delay of 125 ms. In the predictive mode, eye velocity started to build up well before target onset, even during passive stimulation. It was found that the time of initiation of this anticipatory response was closely associated with the time at which the target would have changed direction even though the target could not be seen at this time. Eye velocity measured 100 ms after target onset was negligible in the nonpredictive mode, whereas in the predictive mode, it progressively increased with target velocity, reaching a maximum of 18 degrees/s when target velocity was 50 degrees/s and PD was greater than 240 ms. Examination of the difference in the eye velocity trajectories for the predictive and nonpredictive modes indicated that the greatest contribution of prediction occurred approximately 150 ms after target onset and its effects were evident in the predictive response for at least 300 ms. This effect was reflected in the reaction time between target onset and the occurrence of peak eye velocity. In the nonpredictive mode, this progressively increased from 250 ms to 400 ms as PD increased from 80 to 640 ms, whereas in the predictive mode peak velocity occurred an average of 50 ms earlier for all values of PD. The results demonstrate the significant contribution that predictive processes make to normal ocular pursuit behavior and the importance of timing control in this process. They also indicate that this process is not dependent on volitional control, but can be seen as an automatized response during passive stimulation.

Adaptation, Ocular↗

[Dim the light! Glare problems in a world with ever increasing demands on visual acuity].

Ocular tissue transparency is dependent on the regular lattice configuration of lens and corneal fibres of uniform diameter. Ageing is associated with degeneration of both lens and cornea, which lose some of their structural order and eventually their transparency, though this process is not uniform. The structural changes are local and result in ocular media opacities. When the opacities increase in number and extension, they begin to affect visual acuity. As the loss of acuity becomes clinically significant, we speak of clinically relevant cataract. Retinal exposure to light diffused by intraocular light scattering induces optical glare, one of two forms of glare. The other form is transient glare--i.e., glare due to adaptation problems in an environment with rapidly changing ambient luminance. Contemporary society is characterised by increasing emphasis on visual information in such forms as texts, icons, signs and symbols. The computer revolution has been accompanied by further stress on the importance of the detection and interpretation of written instructions.

Adaptation, Ocular↗

Memory trace of motor learning shifts transsynaptically from cerebellar cortex to nuclei for consolidation.

Adaptation of ocular reflexes is a prototype of motor learning. While the cerebellum is acknowledged as the critical site for motor learning, the functional differences between the cerebellar cortex and nuclei in motor memory formation are not precisely known. Two different views are proposed: one that the memory is formed within the cerebellar flocculus, and the other that the memory is formed within vestibular nuclei. Here we developed a new paradigm of long-term adaptation of mouse horizontal optokinetic response eye movements and examined the location of its memory trace. We also tested the role of flocculus and inferior olive in long-term adaptation by chronic lesion experiments. Reversible bilateral flocculus shutdown with local application of 0.5 microl-5% lidocaine extinguished the memory trace of day-long adaptation, while it very little affected the memory trace of week-long adaptation. The responsiveness of vestibular nuclei after week-long adaptation was examined by measuring the extracellular field responses to the electrical stimulation of vestibular nerve under trichloroacetaldehyde anesthesia. The amplitudes and slopes of evoked monosynaptic field response (N1) of week-long adapted mice were enhanced around the medial vestibular nucleus compared with those of control mice. Chronic flocculus or inferior olive lesions abolished both day and week-long adaptations. These results suggest that the functional memory trace of short-term adaptation is formed initially within the cerebellar cortex, and later transferred to vestibular nuclei to be consolidated to a long-term memory. Both day and week-long adaptations were markedly depressed when neural nitric oxide was pharmacologically blocked locally and when neuronal nitric oxide synthase was ablated by gene knockout, suggesting that cerebellar long-term depression underlies both acquisition and consolidation of motor memory.

Adaptation, Physiological↗

Signal transmission from the suprachiasmatic nucleus to the pineal gland via the paraventricular nucleus: analysed from arg-vasopressin peptide, rPer2 mRNA and AVP mRNA changes and pineal AA-NAT mRNA after the melatonin injection during light and dark periods.

Arg-vasopressin (AVP) containing neurons are one of the output paths from the suprachiasmatic nucleus (SCN), the center of the biological clock. AVP mRNA transcription is controlled by a negative feedback loop of clock genes. Circadian rhythm of melatonin release from the pineal gland is regulated by the SCN via the paraventricular nucleus (PVN). To clarify the transduction system of circadian signals from the SCN to the pineal gland, we determined the effects of melatonin injection (1 mg/kg, i.p.) during light and dark periods on Per2 and AVP mRNAs in the SCN and PVN, in addition to arylalkylamine N-acetyltransferase (AA-NAT) and inducible cAMP early repressor (ICER) mRNAs in the pineal gland of rats using RT-PCR. AVP peptide contents were also measured in the SCN and PVN. AVP content in the SCN decreased during the light period, while no changes were observed in the PVN. In the SCN, Per2 mRNA increased during both light and dark periods. In the PVN, Per2 decreased during the light period and increased during the dark period at 180 min after melatonin injection. In the pineal gland, Per2 mRNA increased between 60 and 180 min after the melatonin injection during the light period, while it did not significantly change during the dark period. The AA-NAT mRNA varied similar to the Per2 mRNA changes. These results might suggest that the different responses to melatonin in the pineal gland during the light and dark periods was originated in the changes of Per2 in the PVN via SCN.

ARNTL Transcription Factors↗

The influence of visual input on the vestibulo-ocular reflex.

In order to stabilise a fixation target on the retina, eye movements have to compensate for head movements. During slow head movements visual feedback can control these eye movements. During fast movements of the head, mainly the vestibulo-ocular reflex (VOR) controls eye movements, as visual feedback is too slow. However, visual feedback is an important factor in controlling the VOR; e.g. the gain of the VOR depends on the distance of the target. This study investigates the influence of retinal image position during fast head movements. The experiments were carried out in five human subjects using scleral search coils. The adaptation of each eye individually to a change of retinal position of a target was examined during head shaking. The change in visual input was carried out by placing Fresnel prisms of different strengths in front of both eyes, thus inducing a change in retinal image position without changing the retinal slip. The results show, that both eyes make the appropriate corrections when the visual input changes, even during fast head-movements. These corrections did not influence the gain of the VOR. From these results we conclude, that retinal image position besides retinal slip has a major influence on the monocular eye movements even at high head rotation frequencies.

Adaptation, Ocular↗

Acute effects of tetrahydrobiopterin on the dynamic characteristics and adaptability of of vestibulo-ocular reflex in normal and flocculus lesioned rabbits.

The acute effects of (6R)-5,6,7,8-tetrahydro-L-biopterin (R-THBP) on the dynamic characteristics of horizontal vestibulo-ocular reflex (HVOR) were examined in chronically prepared alert pigmented rabbits. The HVOR gain was measured by 10 degrees-0.1 Hz sinusoidal oscillation of the turntable in darkness. In control rabbits, intramuscular injection of R-THBP (10 mg/kg) induced an increase of HVOR gain by 0.1-0.2, which lasted for 1-3 h. Sustained 10 degrees-0.1 Hz sinusoidal oscillation of the turntable and screen in the reversed direction induced an adaptive increase of HVOR gain by 0.2 in 3 h, which was not affected by applications of R-THBP. In flocculus lesioned rabbits, the HVOR gain reduced by 23%, and applications of R-THBP no longer induced a HVOR gain increase. These experimental observations suggested that the R-THBP affected on the HVOR dynamics within the cerebellar flocculus or its related neural areas.

Animals↗

The latency of the cat vestibulo-ocular reflex before and after short- and long-term adaptation.

Latencies of normal and adapted feline vestibulo-ocular reflex (VOR) were studied in five cats by applying +/- 20 degrees/s horizontal head velocity steps (4000 degrees/s2 acceleration) and measuring the elicited horizontal or vertical reflex eye responses. Normal VOR latency was 13.0 ms +/- 1.9 SD. Short-term adaptation was then accomplished by using 2 h of paired horizontal sinusoidal vestibular stimulation and phase-synchronized vertical optokinetic stimulation (cross-axis adaptation). For long-term adaptation, cats wore x 0.25 or x 2.2 magnifying lenses for 4 days. The cats were passively rotated for 2 h/day and allowed to walk freely in the laboratory or their cages for the remainder of the time. The latency of the early (primary) adaptive response was 15.2 ms +/- 5.2 SD for cross-axis adaptation and 12.5 ms +/- 3.9 SD for lens adaptation. This short-latency response appeared within 30 min after beginning the adaptation procedure and diminished in magnitude overnight. A late (secondary) adaptive response with latency of 76.8 ms +/- 7.0 SD for cross-axis adaptation and 68.1 ms +/- 8.8 SD for lens adaptation appeared after approximately 2 h of adaptation. It had a more gradual increase in magnitude than the primary response and did not diminish in magnitude overnight. These data suggest that brainstem VOR pathways are a site of learning for adaptive VOR modification, since the primary latency is short and has a similar latency to that of the normal VOR.

Adaptation, Physiological↗

Dynamic properties, interactions and adaptive modifications of vestibulo-ocular reflex and optokinetic response in mice.

Dynamic properties of horizontal vestibulo-ocular reflex (VOR) and optokinetic response (OKR) were studied in mice. The VOR was examined in the dark (VORD), in the light (VORL) and in the condition in which most of the visual field moves synchronously with the head motion (VORF). A mouse and/or a surrounding screen with vertical stripes was rotated sinusoidally, and the gain and phase of eye movements were measured in wide dynamic stimulation ranges. The working conditions of VOR and OKR were supplementary; OKR worked at low speeds of head turn and VOR at high speeds. Examination of VORL and VORF revealed non-linear interaction of VOR and OKR. The continuous sinusoidal head oscillation coupled with the in-phase or the out-of-phase oscillation of the surrounding screen, decreased or increased the VORD gain, and increased or decreased the VORD phase lead, respectively. Continuous oscillation of the surrounding screen increased the OKR gain and decreased the phase delay. These changes of VOR and OKR work to reduce the retinal slip. The present study provides fundamental information concerning the dynamic properties of VOR and OKR and the nature of their adaptive modifications in mice, which have been extensively used in genetic manipulation recently.

Adaptation, Physiological↗

The effect of the rotational magnification of corrective spectacles on the quantitative evaluation of the VOR.

The gain of the vestibulo-ocular reflex (slow-phase eye velocity/chair velocity, measured in the dark) was compared in 11 normal healthy subjects who habitually wore corrective spectacles of varying strength. The rotational magnification (or prismatic effect) induced by habitually wearing corrective spectacles caused the VOR gain measured in darkness to vary systematically with diopter of correction. Even when allowances were made for the inherent variability of measurement of the VOR gain, myopes tended to have lower gains and hyperopes higher gains. This study demonstrates that the clinician should account for spectacle adaptation to properly interpret the results of vestibular function tests.

Adaptation, Ocular↗

Ocular manifestations and complications of acute methyl alcohol intoxication.

The ocular manifestations of acute methyl alcohol intoxication were studied in 24 men during an outbreak in Port Moresby, Papua New Guinea. The visual acuity, pupillary reactions to light, fundal appearances and visual fields were recorded in all patients within 72 hours of ingestion of methanol and again three months later. Three groups were identified. Nine patients had no ocular abnormality (Group 1). Seven patients had only transient ocular abnormalities (Group 2). Eight patients had permanent ocular abnormalities (Group 3). Transient abnormalities included peripapillary oedema, optic disc hyperaemia, diminished pupillary reactions to light, and central scotomata. Permanent ocular abnormalities included optic disc pallor, attenuation of arterioles, sheathing of arterioles, diminished pupillary reaction to light, diminished visual acuity, central scotomata, and other nerve fibre bundle defects. Complete blindness occurred in two patients, while severe visula deficit resulted in four others. The incidence of permanent ocular abnormalities was found to correlate with the incidence of metabolic acidosis (P less than 0.01), and with the stated volume of methanol consumed (P less than 0.05). An inverse correlation was found between stated volume of methanol consumed and onset of blurred vision. The difficulties in management and rehabilitation of these patients are discussed.

Adaptation, Ocular↗

Interocular torsional disparity and visual cortical development in the cat.

1. The present experiments were designed to assess the effects of relatively large optically induced interocular torsional disparities on the developing kitten visual cortex. Kittens were reared with restricted visual experience. Three groups viewed a normal visual environment through goggles fitted with small prisms that introduced torsional disparities between the left and right eyes' visual fields, equal but opposite in the two eyes. Kittens in the +32 degrees goggle rearing condition experienced a 16 degrees counterclockwise rotation of the left visual field and a 16 degrees clockwise rotation of the right visual field; in the -32 degrees goggle condition the rotations were clockwise in the left eye and counterclockwise in the right. In the control (0 degree) goggle condition, the prisms did not rotate the visual fields. Three additional groups viewed high-contrast square-wave gratings through Polaroid filters arranged to provide a constant 32 degrees of interocular orientation disparity. 2. Recordings were made from neurons in visual cortex around the border of areas 17 and 18 in all kittens. Development of cortical ocular dominance columns was severely disrupted in all the experimental (rotated) rearing conditions. Most cells were classified in the extreme ocular dominance categories 1, 2, 6, and 7. Development of the system of orientation columns was also affected: among the relatively few cells with oriented receptive fields in both eyes, the distributions of interocular disparities in preferred stimulus orientation were centered near 0 degree but showed significantly larger variances than in the control condition.(ABSTRACT TRUNCATED AT 250 WORDS)

Adaptation, Ocular↗

Techniques and developments in automated perimetry: a review.

The development of automated perimetry represents one of the major opportunities for clinical advancement over the last 30 years. Compared with the data obtained from equivalent manual procedures, the technique now makes feasible a rapid and reliable static threshold investigation of the visual field and, as a result, has revolutionized the potential of the visual field examination in the diagnosis of ocular and neuro-ophthalmic abnormality. Several perimeters are commercially available, each featuring a variety of stimulus parameters for investigating the visual field and a range of data reduction techniques and displays to aid the clinician in the interpretation of abnormality. The choice of stimulus, however, governs the format of the derived field and thus the efficiency of detecting and assessing a given field defect. In addition, patient-specific variables also influence the visual field profile. This review outlines the techniques used in automated perimetry. In particular, the rationale is summarized for the choice of the major stimulus parameters employed by a given perimeter, such a stimulus type, adaptation level and testing strategy. The techniques available for data display and reduction are reviewed and the extraneous factors influencing the format of the normal differential sensitivity gradient are discussed.

Adaptation, Ocular↗

Dual adaptation and adaptive generalization of the human vestibulo-ocular reflex.

In two experiments, we examined the possibility that the human vestibulo-ocular reflex (VOR) is subject to dual adaptation (the ability to adapt to a sensory rearrangement more rapidly and/or more completely after repeated experience with it) and adaptive generalization (the ability to adapt more readily to a novel sensory rearrangement as a result of prior dual adaptation training). In Experiment 1, the subjects actively turned the head during alternating exposure to a visual-vestibular rearrangement (target/head gain = 0.5) and the normal situation (target/head gain = 0.0). These conditions produced both adaptation and dual adaptation of the VOR but no evidence of adaptive generalization when tested with a target/head gain of 1.0. Experiment 2, in which exposure to the 0.5 gain entailed externally controlled (i.e., passive) whole body rotation, resulted in VOR adaptation but no dual adaptation. As in Experiment 1, no evidence of adaptive generalization was found.

Adaptation, Physiological↗

The effect of melperon on ocular readaptation time, as assessed by a new recording technique.

A new simplified technique recording readaptation time after photo stress, RAT, is described. The psychometric properties in terms of internal consistency and retest reliability were tested, and the effect on RAT after intake of melperon at two different dose levels was investigated and correlated to blood plasma levels. The results show that there was a satisfactory consistency of RAT at each occasion but stability over a 1 month period could not be demonstrated. Significantly dose-dependent changes were recorded after intake of melperon but the prolongation of RAT was not significantly correlated to blood plasma levels.

Adaptation, Ocular↗

Changes in ocular torsion position produced by a single visual line rotating around the line of sight--visual "entrainment" of ocular torsion.

A large- or full-field visual stimulus slowly rotating around the naso-occipital axis of an observer causes both eyes to tort, and many of the factors controlling this optokinetic torsional response have been identified. The present study reports that a single line rotating about the line of sight can cause both eyes to tort in the same direction as the stimulus but with a low gain. We have used the term 'entrainment' to describe this torsional response. This paper reports some of the factors associated with entrainment. Video measures of 3-d eye position were recorded while the subject made settings of a simple visual line to subjective visual horizontal (SVH) and vertical (SVV) using the standard method-of-adjustment paradigm. The visual line was composed of 11 light-emitting diodes; the line subtended a visual angle of 19 degrees, and moved at a constant speed of 4.8 degrees /s. Settings were made in an otherwise darkened room, and also in the light. Subjects were required to maintain fixation of the central LED while making settings from starting positions 10 or 20 degrees either side of gravitational horizontal or vertical. We show that entrainment of ocular torsion by the single moving visual line is low in gain but a reliable and repeatable effect and that (1) there are considerable individual differences between subjects but within-subject consistency, (2) all subjects show larger and more consistent torsional entrainment for lines moving to SVH than lines moving to SVV, (3) the strongest entrainment generally occurs within about 10 degrees of the target position, and (4) entrainment is also present in the light, though with slightly reduced gain.

Adaptation, Ocular↗

A framework for considering the role of afference and efference in the control and perception of ocular position.

It has been well established that extra-retinal information is used in the perception of visual direction and distance. Furthermore, a number of studies have established that both efference copy and afferent discharge contribute to the extra-retinal signal. Despite this, no model currently exists to explain how the signals which arise through oculomotor control contribute to perception. This paper attempts to provide such a framework. The first part of the paper outlines the framework [the cyclopean equilibrium point (EP) model] and considers the binoculus or cyclopean eye from the perspective of a current account of motor control (the EP hypothesis). An existing model is used to describe how the nervous system could utilise available efference copy and afferent extra retinal signals when determining the direction and distance of cyclopean fixation. Although the cyclopean EP model is speculative, it allows for a parsimonious framework when considering the oculomotor contribution to perception. The model has the additional advantage of being consistent with current theories regarding the control and perception of limb movement. The second part of the paper shows that the model is biologically plausible, demonstrates the use of the proposed model in describing the central control of eye movements with regard to non-conjugate peripheral adaptation and reconciles seemingly disparate empirical findings.

Adaptation, Ocular↗

Eye instability in the rabbit induced by vestibular stimulation in the vertical plane.

OBJECTIVE: Sinusoidal vestibular stimulation in the horizontal plane induces periodic eye instability in the intact rabbit and the hypothesis of an intrinsically unstable velocity storage mechanism has been conceived. The present research examined the stability of the vestibulo-ocular reflex (VOR) in the vertical plane, considering that the time constant values of vertical and horizontal VORs differ and that separate regions of the vestibulo-cerebellum affect the horizontal and vertical slow VOR components differently. MATERIAL AND METHODS: Normal pigmented rabbits were sinusoidally oscillated in the dark about their vertical and longitudinal axes to evoke horizontal and vertical eye responses. RESULTS: Frequency and peak-to-peak amplitude stimulation parameters ranged from 0.1 to 0.8 Hz and from 5 degrees to 20 degrees, respectively. During horizontal VOR, periodic alternating drift (PAD) was superimposed on the ocular response, and both peak velocity and period were directly correlated with stimulation amplitude. Vestibular stimulation in the vertical plane induced PAD: the period of vertical PAD was shorter and the amplitude smaller than the corresponding horizontal PAD values. A further difference in vertical PAD occurred in the lack of modulation of period and peak velocity by the stimulus amplitude. CONCLUSION: These results support the hypothesis of different instabilities of the velocity storage mechanism in the vertical and horizontal planes, possibly due to separate sensory-motor systems sub-serving the vertical and horizontal VORs.

Adaptation, Ocular↗