Localization in the frontal plane is not susceptible to manipulation of afferent feedback via the Jendrassik Maneuver.

We have previously shown that registered vergence eye position is altered while participants perform the Jendrassik Maneuver (JM). We proposed that the altered eye position signal registration is due to the effect of the JM which changes the gain of the sensory feedback from the eye muscles, possibly via the activity of non-twitch motoneurons. We conducted two studies to further extend and clarify one of our previous findings by examining whether the JM also affects registered eye position during localization in the frontal plane. Since the non-twitch motoneurons do not receive premotor input from areas involved in the programming of saccades, we hypothesized that localization responses associated with the saccadic system should not be affected by the JM. The data confirmed our prediction. We propose that the non-twitch motoneurons are involved in parametric adjustment of the proprioceptive feedback loops of the vergence but not the version eye movements.

Manipulation of extraocular muscle afference has no effect on higher order perceptual judgments.

Observers perceive targets as farther while performing the Jendrassik Maneuver (JM) suggesting that eye position is registered as more divergent. We examined the effects of the JM perturbation in three studies of perceptual judgment that rely on accurate registration of absolute distance: size constancy, stereoscopic depth, and the magnitude of the Pulfrich illusion. The data showed no significant differences between the JM and control conditions. The lack of an effect may be due to the fact that vergence is not a perfect cue to distance. Furthermore, the relative contribution of extraocular muscle afference to registered eye position may be less significant for higher order perceptual judgments.

Ocular motor measures in migraine with and without aura.

The purpose of this study was to examine basic ocular motor function in individuals with migraine. We used an infrared eye-tracking system to measure horizontal smooth pursuit to a sinusoidal target, saccades to horizontal target displacements of 5-20 degrees , and the stability of fixation in 19 migraine without aura (MoA), 19 migraine with aura (MA) and 19 headache-free control (C) subjects. Eye movement measurements were made at two target displacement rates and against both homogeneous grey and patterned backgrounds. We found no statistically significant differences between migraine and control subjects in any of the eye movement parameters measured, but did find highly significant effects of both target speed and background pattern in all groups. Our results do not provide support for subclinical cerebellar impairment in migraineurs, and do provide evidence that previously described visual abnormalities in migraine are not artefacts of abnormal fixation or eye movements.

Proprioceptive role for palisade endings in extraocular muscles: evidence from the Jendrassik Maneuver.

A proprioceptive hypothesis for the control of eye movements has been recently proposed based on neuroanatomical tracing studies. It has been suggested that the non-twitch motoneurons could be involved in modulating the gain of sensory feedback from the eye muscles analogous to the gamma (gamma) motoneurons which control the gain of proprioceptive feedback in skeletal muscles. We conducted behavioral and psychophysical experiments to test the above hypothesis using the Jendrassik Maneuver (JM) to alter the activity of gamma motoneurons. It was hypothesized that the JM would alter the proprioceptive feedback from the eye muscles which would result in misregistration of eye position and mislocalization of targets. In the first experiment, vergence eye movements and pointing responses were examined. Data showed that the JM affected the localization responses but not the actual eye position. Perceptual judgments were tested in the second experiment, and the results showed that targets were perceived as farther when the afferent feedback was altered by the JM. Overall, the results from the two experiments showed that eye position was perceived as more divergent with the JM, but the actual eye movements were not affected. We tested this further in Experiment 3 by examining the effect of JM on the amplitude and velocity of saccadic eye movements. As expected, there were no significant differences in saccadic parameters between the control and experimental conditions. Overall, the present study provides novel insight into the mechanism which may be involved in the use of sensory feedback from the eye muscles. Data from the first two experiments support the hypothesis that the JM alters the registered eye position, as evidenced by the localization errors. We propose that the altered eye position signal is due to the effect of the JM which changes the gain of the sensory feedback from the eye muscles, possibly via the activity of non-twitch motoneurons.

Saccades in children with spina bifida and Chiari type II malformation.

BACKGROUND: Saccades are essential for optimal visual function. Chiari type II malformation (CII) is a congenital anomaly of the cerebellum and brainstem, associated with spina bifida. OBJECTIVE: To investigate the effects of CII on saccades and correlate saccadic parameters with brain MRI measurements. METHODS: Saccades were recorded in 21 participants with CII, aged 8 to 19, using an infrared eye tracker. Thirty-nine typically developing children served as controls. Participants made saccades to horizontal and vertical target steps. Nineteen participants with CII had MRI. Regression analyses were used to investigate the effects of spinal lesion level, number of shunt revisions, presence of nystagmus, and midsagittal MRI measurements on saccades. RESULTS: Saccadic amplitude gains, asymptotic peak velocities, and latencies did not differ between the control and CII groups (p > 0.01). No significant differences were found between saccadic gains, asymptotic peak velocities or latencies, and spinal lesion level, number of shunt revisions, presence of nystagmus, or MRI measurements. CONCLUSIONS: Saccades were normal in most participants with Chiari II malformation (CII). Neural coding of saccades is robust and is typically not affected by the anatomic deformity of CII.

Accuracy of estimating time to collision using only monocular information in unilaterally enucleated observers and monocularly viewing normal controls.

Since individuals who have lost an eye in early life rely on monocular information, one asked if they would better estimate the time to collision (TTC) with an approaching object based on the monocular cue [(θ/(dθ/dt), i.e. tau] than a control group using only monocular information. Estimates of TTC were measured with a simulated approaching textured object using a staircase procedure. Seven adult observers who were unilaterally enucleated at an early age were compared with 18 normally sighted control observers who viewed the stimuli monocularly. Consistent with previous findings, the majority of the controls (13/18) underestimated TTC. Three enucleated observers had larger estimation errors than the 95% confidence interval of the mean of the control group. One enucleated observer was unable to give reliable results. These results suggest that unilaterally enucleated observers cannot estimate TTC more accurately (and may even be worse) than normal controls when estimates are based on monocular information alone. Further, the majority (83%) of enucleated observers were influenced by perceived distance information derived from the object's initial size when estimating TTC with an approaching object. The use of this other optical variable could account for their reduction in performance. It was suggested that in every day life enucleated individuals make use of as many optical variables as possible to partially compensate for the lack of binocularity.

Egocentric localization: visually directed alignment to projected head landmarks in binocular and monocular observers.

PURPOSE: To determine the accuracy and precision with which humans align moving, non-moving, point-like and linear stimuli to three head landmarks projected to a frontal plane. Monocularly enucleated and binocularly normal subjects, performing monocularly, were tested. METHODS: Experimental tasks consisted of aligning the stimulus, a luminescent target, using a remote steering wheel control, to three projected landmarks; the nose, and the outside edge of each ear. Experiments were performed with a fixed [static] linear stimulus and a small dynamic stimulus, and then with a fixed stimulus at both a very close and an intermediate distance. RESULTS: The data from the monocular enucleated observers showed better accuracy in some conditions but their variable errors were larger than those of the controls. CONCLUSIONS: We propose that, for the alignments of the enucleated monocular subjects, a) the increase in accuracy is consistent with a shift of the egocenter in the direction of the remaining eye, and b) the decrease in precision may be due to the fact that the egocenter does not correspond to the mid-sagittal or median plane. This disparity would require adjustments to be learned in order to perform tasks involving visually directed alignments to the self.

Monocular horizontal OKN in observers with early- and late-onset strabismus.

Several reports on monocular optokinetic nystagmus (OKN) in observers with strabismus have found that asymmetry of OKN tends to occur in both eyes of observers with an early onset of strabismus but only in the deviating eye of those with a later onset of strabismus. Our objective was to quantify and compare the magnitude of the OKN asymmetry in each eye as a function of observer's age at onset of strabismus. We studied monocular OKN in ten observers with early-onset (up to 24 months of age), seven observers with late-onset (after 24 months of age) unilateral strabismus, and 12 normally sighted control observers. In the deviating eye, observers with early-onset strabismus showed large OKN asymmetries in favour of nasalward motion while observers with late-onset strabismus showed smaller OKN asymmetries in that eye. The majority of early- and late-onset observers showed near normal OKN in the non-deviating eye although the early-onset observers showed bilateral asymmetries more often. These findings may be due to both age at onset of strabismus and chronological age and are discussed in terms of the issue of plasticity or recovery of function.

Registered eye position: short- and long-term effects of botulinum toxin injected into eye muscle.

Botulinum toxin is sometimes injected into human eye muscles as an alternative to surgery in the correction of strabismus. Within minutes of botulinum injections into ungulate eye muscles, proprioceptive discharge from muscle spindles decreases dramatically. It is only over 7-48 h, however, that surgically treated strabismus patients usually show an altered proprioceptive signal about eye position, presumably from the palisade endings attached to the global multiply innervated fibers. How quickly will botulinum toxin alter proprioceptive registration of eye position in humans? First, to examine the short-term effects, we measured open-loop pointing responses (which requires knowledge of eye position) in six strabismus patients preinjection and then over a 45 min postinjection period, and in six normal controls over the same time period. Second, to examine the long-term effects, 13 strabismus patients were tested preinjection and then daily over the next 3 weeks, and three normal controls over the same time period. We compared their open-loop pointing responses with the injected eye fixating the target to the photographically determined position of the occluded other eye (a measure of where the patient would point if eye position were determined by efference, not proprioception). There were three groups of patients: esotropes with no previous injection, exotropes with no previous injection, and exotropes with previous injection. First, all patients showed significant correction of their tropias. Second, over the short-term, there was no difference in pointing responses found between the patients and the controls (t(18) = -1.427, P = 0.1706). Third, over the long-term, however, the difference between the pointing responses and eye position information was compared among the four groups across four posttests and a significant difference found (F3,12 = 58.988, P < 0.00001). Only in patients with no previous injections was there altered proprioceptive feedback about eye position. Also, injections into the medial rectus induced a significantly greater proprioceptive response than those injected into the lateral rectus. In humans, botulinum toxin alters proprioception from eye muscles only over the long-term. We suggest that the toxin temporarily affects proprioceptive feedback from palisade endings.

The Cyclops effect in adults: sighting without visual feedback.

When asked to look through a tube, younger children place it at the bridge of the nose, and not over one eye: the Cyclops effect. This is a natural response to a median plane egocenter. With maturity, the Cyclops effect disappears as we learn to overcome the consequences of an egocenter between the two eyes, and instead, to use the "preferred" eye. We videotaped adults (n = 14) and children with normal vision (n = 30), children with comitant strabismus (n = 14), and adults and children (n = 14) with one eye enucleated as they attempted to look through a plastic tube. Immediately in front of the face was a liquid crystal window that could be either transparent or opaque. As the tube was raised, the window was made opaque--blocking sight of the target, their hands, and the tube. Most binocular observers placed the tube approximately at the bridge of the nose. This was significantly different from the response of the enucleated observers who put the tube 75% of the way to the remaining eye (P = 0.0001). All observers align, on average, with the measured location of their egocenter when asked to perform a monocular task without visual cues. Deprived of visual feedback, binocular observers show the Cyclops effect, regardless of age.

Vertical latent nystagmus component and vertical saccadic asymmetries in subjects with dissociated vertical deviation.

PURPOSE: This study was conducted to quantify the vertical component of a latent nystagmus observed in subjects with dissociated vertical deviation (DVD), as well as to provide further evidence for vertical saccadic asymmetries in these individuals. METHODS: Binocular eye movements of subjects with DVD were recorded in two dimensions using a noninvasive video-based eye tracker while cover/uncover tests, alternate cover tests, and vertical saccades were performed. RESULTS: A small amplitude (1.5 degrees or less) vertical component of latent nystagmus can be observed in some subjects with DVD and is larger in the deviating eye than in the viewing eye. The frequency of the vertical nystagmus component is the same in each eye for any given fixation condition but may change depending on which eye is fixating. DVD in the presence of a vertical component of latent nystagmus can be adequately modeled by the algebraic sum of an exponentially decreasing velocity DVD and a nystagmus with an exponentially decreasing slow phase velocity. In general, the occluded eyes of DVD subjects make smaller downward saccades than the viewing eyes. CONCLUSIONS: It is possible but not obligatory that DVD subjects will have a vertical component of latent nystagmus. Algebraic summation of an exponentially decreasing velocity DVD and a vertical component of latent nystagmus provides a more parsimonious explanation of the observed saccadic eye movements than modeling the DVD itself as a combination of vergence and saccadic movements. Subjects with DVD show a range of saccadic yoking from nearly complete saccadic conjugacy to nearly complete dissociation.

A comparison of contrast letter thresholds in unilateral eye enucleated subjects and binocular and monocular control subjects.

We previously reported that unilaterally eye enucleated subjects show superior contrast letter acuity to normally sighted monocular viewing control subjects. We suggested that reorganization of the visual system in the enucleated subjects may compensate for their loss of binocularity. Here we measured contrast letter acuity in normally sighted binocular control subjects and compared these results to previously published results of eye enucleated subjects and monocular viewing control subjects. We found equivalent performance between enucleated subjects and binocular control subjects, suggesting that performance of enucleated subjects might be due to some form of neural summation.

Head turn in 1-eyed and normally sighted individuals during monocular viewing.

OBJECTIVE: To determine the incidence and magnitude of head turn in persons unilaterally enucleated at an early age and in normally sighted persons patched monocularly. SETTING: The Hospital for Sick Children, Toronto, Ontario. PARTICIPANTS: Fifty-two unilaterally enucleated children and adults without nystagmus (median age, 10 years) who were enucleated at an early age (median age, 18 months) due to retinoblastoma and 28 normally sighted children and adults. METHODS: Enucleated subjects were videotaped while walking 15 m toward a camera under 2 conditions: (1) fixation relaxed (just looking at the camera) and (2) fixation forced (trying to identify a small fixation target on the camera). Control subjects were tested in the fixation forced condition only. Head turn incidence and magnitude were independently rated. Three categories of head turn were used: "obvious" (> 10 degrees), "small" (5 degrees-10 degrees), and "no" (0 degree-4 degrees). RESULTS: In the fixation relaxed condition, 22 (42%) of 52 enucleated subjects exhibited head turn; when fixation was forced, the incidence increased to 25 (58%) of 43 subjects. Head turn was virtually always in the direction of the missing eye. Incidence and magnitude of head turn were unrelated to age at enucleation or number of years since enucleation. In the control group, there was no consistent finding of head turn across subjects when 1 eye was patched. CONCLUSIONS: One-eyed children frequently exhibit head turn unrelated to the presence of nystagmus. The direction of the head turn is "adaptive" because occlusion by the nose in the lower contralateral field is reduced.

Vertical eye position control in darkness: orbital position and body orientation interact to modulate drift velocity.

How stable is vertical eye-in-head position control in darkness when no visual targets are present? We evaluated this while varying both body-in-space orientation and eye-in-orbit position in six subjects who were free from oculomotor/vestibular disease. Vertical eye movements were monitored using a CCD-video tracking system, and results were confirmed on one subject with the magnetic search coil. Three body orientations were used: (1) seated upright; (2) supine; and (3) prone. In each of these body orientations starting eye-in-orbit position was varied in quasi-random order from -20 to +20 deg, while vertical eye drift was monitored for a 90 sec period at each position. Subjects were instructed to hold their eyes as steady as possible. The relationship between body orientation/eye position and vertical eye drift velocity was examined using a linear regression technique. In contrast to prior clinical reports, normals exhibit a vertical nystagmus/drift in darkness. Moreover, slow-phase eye velocity was found to be dependent on eye-in-orbit position in the upright and supine body orientations. This pattern of eye drift mirrors Alexander's Law, with significantly increased drift velocities when subjects looked in the direction of their re-centering saccades (P < 0.05 or better). Body-in-space orientation also modulated the eye drift velocity, with significant differences in rate of eye drift (P < 0.05 or better) between extremes of body orientation (supine and prone) for five out of six subjects. The stability of the vertical oculomotor control system in the absence of visual input is strongly affected by body-in-space orientation and eye-in-orbit position: manipulating either of these variables results in non-random patterns of drift. These results are discussed using a multiple-input model of vertical eye-in-head position control.

Dissociated vertical deviation: head and body orientation affect the amplitude and velocity of the vertical drift.

PURPOSE: Five subjects with dissociated vertical deviation (DVD) were studied to determine if the amplitude or velocity of the vertical components of the DVD were affected by head/body orientation with respect to gravity. METHODS: Deviations were measured in head upright, head supine, and supine positions, with head hanging postures using a binocular CCD video-based infrared eye tracker. Subjects were required to fixate a target presented in the primary position during alternate or cover/uncover tests. RESULTS: Amplitude and velocity of DVD both in onset and recovery were affected by head/body orientation with respect to gravity. In four of five subjects, the amplitude of the DVD was asymmetric between the two eyes when the head was upright. When the head/body was moved from an upright to a supine with head hanging backward condition, the amplitude of the DVD in the two eyes inverted. The eye with the larger DVD in the upright position had a smaller DVD in the head-hanging orientation. A similar relationship existed between velocity and head/body orientation. We found that DVD velocity increased with amplitude. CONCLUSIONS: Passive effects of gravity on the eye-inorbit do not influence DVD magnitude or frequency of occurrence. The data suggest, however, that otolithic and possibly neck afferent inputs play a role in DVD magnitude and may be a part of the etiology of the condition.

Learning to look with one eye: the use of head turn by normals and strabismics.

When asked to look through a tube, young children (normal, strabismic, monocularly enucleated) place it between the eyes, while older children turn the head or shut one eye. We videotaped 174 children (normals and strabismics, 2-17 yr of age) and 16 normal adults to find out when and why head turn occurs. In learning to look with one eye, children progressed through a sequence of four responses, categorized by age or amount of head turn. Binocular children use head turn apparently to avoid diplopia, then, most learn to shut one eye. Adults, forced to use the "non-preferred" eye, revert to turning the head.

Contrast letter thresholds in the non-affected eye of strabismic and unilateral eye enucleated subjects.

To investigate the effects of visual disruption on contrast letter thresholds of the non-affected eye, subjects with one eye enucleated, strabismic subjects using the non-deviating eye and normal control subjects were asked to identify letters on eye charts and single letter cards which varied in contrast (between 4 and 96%) and size. At all contrast, contrast letter acuity of eye enucleated subjects was superior to both normal control subjects and strabismic subjects. Early onset strabismic subjects (onset < 24 months) showed inferior performance to normal control subjects at all contrasts of 25% and above. Late onset strabismic subjects showed normal performance at all contrasts, except for high contrast single letters, where performance was inferior to normal control subjects. Further, for all subjects groups, performance on letter charts was similar to performance on single letter cards. We conclude that disruption to the visual system caused by eye enucleation or strabismus is not equivalent. These differences may be due to intrinsic differences between the visual systems of eye enucleated subjects and strabismic subjects and/or to the profound differences in deprivation caused by the two conditions.

Alignment ability of strabismic and eye enucleated subjects on the horizontal and oblique meridians.

For normal sighted observers visual performance is often superior on the principal meridians than on the oblique. There has been no clear consensus on whether disruption of the visual system affects performance on orientation sensitivity tasks. Here we compare the abilities of normally sighted subjects tested monocularly, subjects with one eye enucleated and strabismic subjects using the non-deviating eye, in an orientation task. Subjects were asked to align a dot with a bar that was oriented either horizontally or on the oblique. For all groups, alignments were significantly more accurate and precise for the horizontal bar as compared to the oblique bar. Normally sighted subjects were significantly more precise on alignments in the horizontal and oblique planes than strabismic subjects, using the non-deviating eye. Precision for eye enucleated subjects was similar to that of normally sighted subjects. Precision of alignments did not correlate to the age at diagnosis of strabismus or to depth of amblyopia in strabismus. We conclude that for alignment ability, the disruption of visual development produced by enucleation of eye is not equivalent to that produced by strabismus. This could represent an underlying difference in the visual system between these two groups.