Horizontal Optokinetic Nystagmus Research Articles

Eye Movement Abnormalities in Joubert Syndrome

Joubert syndrome is a genetic disorder characterized by hypoplasia of the midline cerebellum and deficiency of crossed connections between neural structures in the brain stem that control eye movements. The goal of the study was to quantify the eye movement abnormalities that occur in Joubert syndrome. Eye movements were recorded in response to stationary stimuli and stimuli designed to elicit smooth pursuit, saccades, optokinetic nystagmus (OKN), vestibulo-ocular reflex (VOR), and vergence using video-oculography or Skalar search coils in 8 patients with Joubert syndrome. All patients underwent high-resolution magnetic resonance imaging (MRI). All patients had the highly characteristic molar tooth sign on brain MRI. Six patients had conjugate pendular (n = 4) or see-saw nystagmus (n = 2); gaze holding was stable in four patients. Smooth-pursuit gains were 0.28 to 1.19, 0.11 to 0.68, and 0.33 to 0.73 at peak stimulus velocities of 10, 20, and 30 deg/s in six patients; smooth pursuit could not be elicited in four patients. Saccade gains in five patients ranged from 0.35 to 0.91 and velocities ranged from 60.9 to 259.5 deg/s. Targeted saccades could not be elicited in five patients. Horizontal OKN gain was uniformly reduced across gratings drifted at velocities of 15, 30, and 45 deg/s. VOR gain was 0.8 or higher and phase appropriate in three of seven subjects; VOR gain was 0.3 or less and phase was indeterminate in four subjects. The abnormalities in gaze-holding and eye movements are consistent with the distributed abnormalities of midline cerebellum and brain stem regions associated with Joubert syndrome.

Torsional optokinetic nystagmus in strabismus

Abstract Purpose Torsional optokinetic Nystagmus (tOKN) in patients with strabismus since childhood has not been previously evaluated.The authors investigated the optokinetic response in horizontal, vertical and torsional directions in strabismus patients and in age‐matched normal volunteers. Methods Monocular torsional, horizontal and vertical eye movements were recorded in 16 subjects with childhood strabismus and 15 normal volunteers.Constant velocity horizontal (nasalward and temporalward) and vertical(upward and downward) OKN stimuli were used at 10°/s, 20°/s and 40°/s.Torsional(intorsion and extorsion)OKN stimuli were rotated at velocities of 40° and 400°/s. Results OKN responses from strabismus patients produced significant asymmetric responses in horizontal and vertical directions. The nasalward response was significantly greater than the temporalward and upward response was greater than downward. A significant high incidence of absent tOKN was present in both intorsion and extorsion. Eight of the 15 patients tested did not respond to any stimulus in either direction in their non‐dominant eye and 4 showed no response in their dominant eye. Conclusion Torsional OKN is dramatically affected in the presence of strabismus with a high incidence of no response. The possibility of a lack of development in the binocular cortical structures that respond to torsional motion could explain these findings.

Expansion of Visual Space During Optokinetic Afternystagmus (OKAN)

The mechanisms underlying visual perceptual stability are usually investigated using voluntary eye movements. In such studies, errors in perceptual stability during saccades and pursuit are commonly interpreted as mismatches between actual eye position and eye-position signals in the brain. The generality of this interpretation could in principle be tested by investigating spatial localization during reflexive eye movements whose kinematics are very similar to those of voluntary eye movements. Accordingly, in this study, we determined mislocalization of flashed visual targets during optokinetic afternystagmus (OKAN). These eye movements are quite unique in that they occur in complete darkness and are generated by subcortical control mechanisms. We found that during horizontal OKAN slow phases, subjects mislocalize targets away from the fovea in the horizontal direction. This corresponds to a perceived expansion of visual space and is unlike mislocalization found for any other voluntary or reflexive eye movement. Around the OKAN fast phases, we found a bias in the direction of the fast phase prior to its onset and opposite to the fast-phase direction thereafter. Such a biphasic modulation has also been reported in the temporal vicinity of saccades and during optokinetic nystagmus (OKN). A direct comparison, however, showed that the modulation during OKAN was much larger and occurred earlier relative to fast-phase onset than during OKN. A simple mismatch between the current eye position and the eye-position signal in the brain is unlikely to explain such disparate results across similar eye movements. Instead, these data support the view that mislocalization arises from errors in eye-centered position information.

Horizontal and Vertical Look and Stare Optokinetic Nystagmus Symmetry in Healthy Adult Volunteers

Look optokinetic nystagmus (OKN) consists of voluntary tracking of details in a moving visual field, whereas stare OKN is reflexive and consists of shorter slow phases of lower gain. Horizontal OKN is symmetrical in healthy adults, whereas symmetry of vertical OKN is controversial. Horizontal and vertical look and stare OKN symmetry was measured, and the consistency of individual asymmetries and the effect of varying stimulus conditions were investigated. Horizontal and vertical look and stare OKN gains were recorded in 15 healthy volunteers (40 degrees /s) using new methods to delineate look and stare OKN. Responses with right and left eye viewing were compared to investigate consistency of individual OKN asymmetry. In a second experiment, the symmetry of stare OKN was measured in nine volunteers varying velocity (20 degrees /s and 40 degrees /s), contrast (50% and 100%), grating contrast profile (square or sine wave), and stimulus shape (full screen or circular vignetted). There was no horizontal or vertical asymmetry in look or stare OKN gain for all volunteers grouped together. However, individual vertical asymmetries were strongly correlated for left and right eye viewing (look: r = 0.77, P = 0.0008; stare: r = 0.75, P = 0.001) and for look and stare OKN (r = 0.66, P = 7.3 x 10(-5)) because of a strong correlation for downward moving stimuli (r = 0.73, P = 0.002). Horizontal and vertical asymmetries were not significantly affected by variations in stimulus parameter. Although no horizontal or vertical OKN asymmetries existed for volunteers grouped together, vertical OKN was characterized by idiosyncratic asymmetries that remained consistent for an individual. Look and stare OKN gain is strongly associated for downward moving stimuli.

The Effect of Aging on Torsional Optokinetic Nystagmus

The effect of aging on torsional optokinetic nystagmus (tOKN) is unknown. The authors investigated changes in tOKN associated with aging in a group of healthy subjects. Monocular torsional eye movements were recorded from 30 subjects between 19 and 72 years of age. Constant-velocity rotary stimuli in clockwise and counterclockwise directions were used to elicit tOKN at 40 degrees /s and 400 degrees /s. The number of subjects in whom tOKN could not be detected increased with age and was consistent in both directions of stimulation and at both angular velocities of stimulation. tOKN appears to fail increasingly with age, in contrast to previous reports of horizontal and vertical OKN systems. This indicates that the ability to respond to rotary motion is more sensitive to the effects of aging.

Optokinetic nystagmus in harbor seals ( Phoca vitulina)

Harbor seals experience motion due to self-motion and to movement in the external world. However, motion vision has not been studied yet in marine mammals moving in the underwater world. To open up this research, optokinetic nystagmus (OKN) as a basic motion sensing and retinal image stabilizing reflex was studied in four harbor seals during stimulation with moving black-and-white stripe patterns. All seals responded with optokinetic eye movements. Detailed measurements obtained with one animal revealed a moderate gain for horizontal binocular OKN. Monocularly stimulated, the seal displayed a symmetrical OKN with slightly stronger responses to leftward moving stimuli, and, surprisingly, a symmetrical OKN was found in the vertical domain.

Optokinetic Nystagmus as a Measure of Visual Function in Severely Visually Impaired Patients

To evaluate the efficacy of using optokinetic nystagmus (OKN) as an objective measurement of vision in severely visually impaired patients, in whom it is difficult to measure visual function reliably. Objective visual acuity (VA) measurements would be useful in the pre-and postoperative assessment of severely visually impaired patients who are potential candidates for visual rehabilitation strategies, such as retinal prostheses, neural and stem cell transplantation, and molecular approaches. Full-field visual stimuli were used to evoke horizontal OKN responses in 17 subjects. Eye movements were recorded and analyzed to determine the maximum stimulus velocity (V(max)) at which subjects could maintain an OKN response. This endpoint was compared to logMAR VA and Goldmann visual field (VF) test results. V(max) was dependent on VA, VF, and the spatial frequency (SF) of the stimulus, yielding the equation V(max) = 14.2 . log(VA) - 6.20 . log(SF) + 0.22 . VF + 25.0. The findings suggest that V(max) in the presence of full-field OKN stimuli may provide an objective measure of VA and peripheral vision. OKN testing may be useful as an additional, more objective means of assessing visual function in a select group of severely visually impaired patients who are being considered as candidates for new visual rehabilitative strategies.

Rotational and translational optokinetic nystagmus have different kinematics

We studied the dependence of ocular torsion on eye position during horizontal optokinetic nystagmus (OKN) elicited by random-dot translational motion (tOKN) and prolonged rotation in the light (rOKN). For slow and quick phases, we fit the eye-velocity axis to vertical eye position to determine the tilt angle slope (TAS). The TAS for tOKN was 0.48 for both slow and quick phases, close to what is found during translational motion of the head. The TAS for rOKN was less for both slow (0.11) and quick phases (0.26), close to what is found during rotational motion of the head. Our findings are consistent with the notion that translational and rotational optic flow are processed differently by the brain and that they produce different 3-D eye movement commands that are comparable to the different commands generated in response to vestibular signals when the head is actually translating or rotating.

Eye movement deficits in children with posterior fossa tumors

Purpose: To evaluate pre- and postsurgical eye movement abnormalities in children with posterior fossa tumors. Methods: Conjugate and vergence eye movements were recorded with inferior rectus video-oculography in 25 children with posterior fossa (PF) tumors after resection of the tumor. Several children were also tested presurgically. Horizontal smooth pursuit (SPh) was elicited with a sinusoidally moving target (±10°, peak velocity, 30°/s). Horizontal and vertical OKN, optokinetic nystagmus, was assessed with a high contrast square-wave grating moving at 15, 30, and 45°/s.

Neuronal Substrates of Motor Learning in the Velocity Storage Generated During Optokinetic Stimulation in the Squirrel Monkey

Chronic motor learning in the vestibuloocular reflex (VOR) results in changes in the gain of this reflex and in other eye movements intimately associated with VOR behavior, e.g., the velocity storage generated by optokinetic stimulation (OKN velocity storage). The aim of the present study was to identify the plastic sites responsible for the change in OKN velocity storage after chronic VOR motor learning. We studied the neuronal responses of vertical eye movement flocculus target neurons (FTNs) during the optokinetic after-nystagmus (OKAN) phase of the optokinetic response (OKR) before and after VOR motor learning. Our findings can be summarized as follows. 1) Chronic VOR motor learning changes the horizontal OKN velocity storage in parallel with changes in VOR gain, whereas the vertical OKN velocity storage is more complex, increasing with VOR gain increases, but not changing following VOR gain decreases. 2) FTNs contain an OKAN signal having opposite directional preferences after chronic high versus low gain learning, suggesting a change in the OKN velocity storage representation of FTNs. 3) Changes in the eye-velocity sensitivity of FTNs during OKAN are correlated with changes in the brain stem head-velocity sensitivity of the same neurons. And 4) these changes in eye-velocity sensitivity of FTNs during OKAN support the new behavior after high gain but not low gain learning. Thus we hypothesize that the changes observed in the OKN velocity storage behavior after chronic learning result from changes in brain stem pathways carrying head velocity and OKN velocity storage information, and that a parallel pathway to vertical FTNs changes its OKN velocity storage representation following low, but not high, gain VOR motor learning.

Brainstem and cerebellar fMRI-activation during horizontal and vertical optokinetic stimulation

Animal studies have shown that not only cortical, but also brainstem and cerebellar areas are involved in the initiation and generation of optokinetic nystagmus (OKN), e.g., cortico-(pretecto)pontine-olivo-cerebellar pathways. The aim of this fMRI study was to identify and differentiate brainstem and cerebellar areas involved in horizontal and vertical OKN (h/vOKN) in humans. In a group of nine healthy volunteers, hOKN and vOKN were statistically compared with a stationary control condition. There were common activated regions for hOKN and vOKN directions located in the transition zone between the posterior thalamus and the mesencephalon bilaterally covering the pretectal nucleus complex, which is known to be a major structure within the afferent branch of the optokinetic system. Furthermore, during hOKN, activation occurred bilaterally in the mediodorsal and dorsolateral ponto-medullary brainstem, which could be best attributed to the reticular formation, especially the paramedian pontine reticular formation (PPRF). For vOKN, additional activated areas in the dorsal mesencephalic brainstem could be best localized to the ocular motor nuclei and the rostral interstitial nucleus of the medial longitudinal fasciculus (riMLF). For both OKN directions, the cerebellar activation was localized in the oculomotor vermis (declive VI, folium and tuber VIIA/B, in part pyramis VIIIA), and the flocculus bilaterally as well as widespread in the cerebellar hemispheres. In conclusion, fMRI allowed first attributions of neuronal substrates in the cerebellum and brainstem to hOKN and vOKN in humans. Consistent with the animal data, the dorsal ponto-medullary routes were involved bilaterally for hOKN, whereas the rostral mesencephalic routes were involved for vOKN.

Eye Movement Abnormalities in Alzheimer Disease: Case Presentation and Literature Review

PurposeTo describe unusual eye movements in a patient with probable Alzheimer disease (AD) who presented with complaints of loss of balance and inability to read. In view of the increasing prevalence of AD in our aging population, it is also our purpose to review the literature regarding AD, as well as the reports of neuro-ophthalmic abnormalities.MethodEye movement recordings were obtained using a RV-275 Saccadic Velocity Recorder (Tracousitics®, Inc.). Horizontal saccades, ocular pursuit, optokinetic nystagmus, and eye movements while reading were recorded.ResultsEye movement recordings revealed the presence of saccadic dysmetria, pathologic small square wave jerks, saccadic pursuit, and irregular optokinetic nystagmus. Eye movements while reading were anomalous showing difficulty in the initiation of reading behaviour and poor stepwise progression through the text.ConclusionsInability to read is a frequent complaint in patients diagnosed with probable AD. In these cases, eye movements should be clinically assessed for subtle abnormalities and further assessment with eye movement recordings may reveal significant disruption in eye movement capability.

Spatial orientation of optokinetic nystagmus and ocular pursuit during orbital space flight.

On Earth, eye velocity of horizontal optokinetic nystagmus (OKN) orients to gravito-inertial acceleration (GIA), the sum of linear accelerations acting on the head and body. We determined whether adaptation to micro-gravity altered this orientation and whether ocular pursuit exhibited similar properties. Eye movements of four astronauts were recorded with three-dimensional video-oculography. Optokinetic stimuli were stripes moving horizontally, vertically, and obliquely at 30 degrees/s. Ocular pursuit was produced by a spot moving horizontally or vertically at 20 degrees/s. Subjects were either stationary or were centrifuged during OKN with 1 or 0.5 g of interaural or dorsoventral centripetal linear acceleration. Average eye position during OKN (the beating field) moved into the quick-phase direction by 10 degrees during lateral and upward field movement in all conditions. The beating field did not shift up during downward OKN on Earth, but there was a strong upward movement of the beating field (9 degrees) during downward OKN in the absence of gravity; this likely represents an adaptation to the lack of a vertical 1-g bias in-flight. The horizontal OKN velocity axis tilted 9 degrees in the roll plane toward the GIA during interaural centrifugation, both on Earth and in space. During oblique OKN, the velocity vector tilted towards the GIA in the roll plane when there was a disparity between the direction of stripe motion and the GIA, but not when the two were aligned. In contrast, dorsoventral acceleration tilted the horizontal OKN velocity vector 6 degrees in pitch away from the GIA. Roll tilts of the horizontal OKN velocity vector toward the GIA during interaural centrifugation are consistent with the orientation properties of velocity storage, but pitch tilts away from the GIA when centrifuged while supine are not. We speculate that visual suppression during OKN may have caused the velocity vector to tilt away from the GIA during dorsoventral centrifugation. Vertical OKN and ocular pursuit did not exhibit orientation toward the GIA in any condition. Static full-body roll tilts and centrifugation generating an equivalent interaural acceleration produced the same tilts in the horizontal OKN velocity before and after flight. Thus, the magnitude of tilt in OKN velocity was dependent on the magnitude of interaural linear acceleration, rather than the tilt of the GIA with regard to the head. These results favor a 'filter' model of spatial orientation in which orienting eye movements are proportional to the magnitude of low frequency interaural linear acceleration, rather than models that postulate an internal representation of gravity as the basis for spatial orientation.

Quantitative analysis of horizontal and vertical optokinetic nystagmus and optokinetic after-nystagmus in the cat

This study reported on the horizontal optokinetic nystagmus (OKN) and vertical OKN of cats under the same conditions with quantitative parameters. Using the search coil method, the horizontal and vertical OKN was investigated in 5 alert cats in an upright position. As the optokinetic stimulus, a stepped random dot pattern was used. We recorded the quantitative parameters in both the horizontal and vertical OKN (for the direct pathway parameters, initial fast rise and fast fall; for the indirect pathway parameters, steady state slow phase velocity [SPV] and the optokinetic after-nystagmus [OKAN] area) in cats. The SPV of the horizontal OKN increased with the stimulus amplitude up to 40-60 degrees/s but saturated thereafter (in some cats even more). Right and left OKN were almost symmetrical. The SPV of the downward OKN increased with the stimulus amplitude up to 20 degrees/s but saturated thereafter. This was lower than the horizontal OKN. On the other hand, the SPV of the upward OKN was weak and irregular. As for the OKAN, the right and left OKAN was also almost symmetrical. A downward OKAN was also observed but was weaker than the horizontal OKAN. A fast fall in the SPV of the OKAN was observed in the horizontal and downward OKN. On the other hand, there was little upward OKAN. OKN in cats was composed of both a direct pathway and an indirect pathway. This study suggested that directional differences of OKN were mainly responsible for the indirect pathway. Both the direct and indirect pathways of cats were smaller than those of monkeys. This suggested that the differences in OKN between cats and monkeys were mainly responsible for the direct pathway.

Eye–neck coupling during optokinetic responses in head-fixed pigeons ( Columba livia): influence of the flying behaviour

The effects of the behavioural context on the properties of slow and fast phases of the horizontal optokinetic nystagmus (OKN) and on the electromyographic neck response (EMG) were investigated in head-fixed pigeons. Responses in two situations were compared: (i) animals were hung in a harness (‘resting' condition); (ii) animals in harness were subjected to a frontal airflow that provoked a flight posture (‘flying' condition). During optokinetic stimuli the neck muscles responded in synchrony and in synergy with the eye nystagmus in both the ‘resting’ and the ‘flying’ conditions. In the ‘resting’ condition the neck activity was essentially correlated to the slow phase velocity of the eyes (eye SPV) whereas in the ‘flying’ condition, the neck response was also correlated to the eye position. The neck response was independent of the retinal slip velocity during the OKN. The velocity of the slow and fast phases of the OKN was not modified by flight. However, the ‘flying’ condition provoked an increase of the neck response by augmenting both its velocity gain (neck EMG/eye SPV) and its position gain (neck EMG/eye position). These results show that although an optokinetic stimulation results in synchronised eye and head motor commands in head-fixed pigeons, only the head motor command is modified by the behavioural context (‘flying' vs. ‘resting’). This strategy could help pigeons in reorienting their gaze during the flight.

Optokinetic nystagmus in strabismus: are asymmetries related to binocularity?

Strabismus may be associated with an asymmetry of monocular horizontal optokinetic nystagmus (OKN). It is unclear whether OKN asymmetries are associated with deficiency in binocular and/or stereovision. In the current study, patients with different degrees of binocularity were investigated. OKN was examined in the dominant and nondominant eyes of four groups of patients: (1) no measurable binocularity (NB), (2) poor binocularity (PB)-that is, showing binocularity on the Bagolini Test and/or rudimentary stereovision, (3) good binocularity (GB) with good stereoacuity after squint surgery, and (4) a control group. Monocular OKN was elicited with black-and-white stripes moving temporally to nasally (TN) or nasally to temporally (NT) at velocities of 15, 30, 45, and 60 deg/s. Eye movements were recorded with infrared oculography. Only subjects in the NB group showed a significant OKN asymmetry, with preference for TN stimulation in dominant and nondominant eyes. Subjects with PB did not have significant OKN asymmetries but reduced OKN gains in both stimulus directions. Subjects with GB had normal mean OKN gains without asymmetry. Larger OKN asymmetries were correlated with younger age at detection of strabismus if NB and GB were grouped together, but not if each group was analyzed separately. For the first time, a large groups of patients classified by level of binocular vision has been investigated. The results show that OKN gain and asymmetry are associated with the development of binocular vision. OKN investigation may be helpful to identify patients with binocularity or binocular potential in strabismus.

Percept-related changes in horizontal optokinetic nystagmus at different body orientations in space.

Large-field motion of the visual environment is a powerful stimulus to induce the perception of contra-directional self-motion in a stationary observer. We investigated the interrelations between horizontal optokinetic nystagmus and subjective states of motion perception under variation of subjects' orientation with respect to gravity. Subjects were tested sitting upright and lying supine, and signalled transitions between object- and self-motion perception whilst viewing an optokinetic stimulus rotating about the subjects' longitudinal axis at a range of angular velocities. Optokinetic stimulation in the supine condition resulted in subjects perceiving a graviceptive conflict and the illusory perception of whole body tilt in a direction opposite to optokinetic stimulus rotation, whereas during upright viewing the axis of stimulus rotation was aligned with the direction of gravity and thus did not result in a conflict or perception of tilt. In both postures, self-motion perception coincided with an increased deviation of mean horizontal gaze position in the perceived direction of heading with a concurrent reduction in optokinetic nystagmus slow-phase gain. Slow-phase gain was also significantly reduced in the supine position as well as at increasing stimulus velocities. The results demonstrate that spontaneous transitions between the perception of object-motion and that of self-motion consistently coincide with spatial attentional and orientational strategies, shifting from passive monitoring to active oculomotor exploration and anticipation.

Visual direction-selective neurons in the pretectum of the rainbow trout

In mammals, the essential neuronal substrate for the generation of the horizontal optokinetic nystagmus (hOKN) are the nucleus of optical tract (NOT) and the dorsal terminal nucleus (DTN). The medial terminal nucleus (MTN) is thought to be involved in vertical OKN control. Characteristic for all of these neurons is a high-direction selectivity. Although behavioural hOKN experiments in different fish species show comparability to mammals, little is known about the neuronal OKN control in fish. In preceding studies, we demonstrated that the rainbow trout has a nearly symmetrical monocular hOKN at low stimulus speeds. With increasing visual stimulus speeds (>14°/s), the monocular hOKN becomes asymmetrical with a temporo to nasal preferred direction. For visual stimulation, we presented random-dot-patterns projected by a planetarium inside a perimeter. We tested four rotation axes of the planetarium, yaw (0°–180°), roll (90°–270°), diagonal (45°–225°) and anti-diagonal (135°–315°). In every position, the visual stimulus turned in clockwise and counter-clockwise direction. In a subregion of the pretectum of nine fish, we recorded 47 direction-selective neurons. Analysis of tuning-curves and preferred direction vectors show that these neurons encode both horizontal (yaw) and vertical (roll) visual stimulus directions. These results suggest that the control of horizontal and vertical OKN might not segregate into different nuclei in fish.

Directional effect of inactivation of the nucleus of the optic tract on optokinetic nystagmus in the cat

The goal of the present investigation was to elucidate the role of the nucleus of the optic tract and the dorsal terminal nucleus of the accessory optic system (NOT-DTN) for slow eye movements other than horizontal. Retinal slip neurons in the NOT-DTN in the awake behaving cat respond direction selectively to the ipsiversive component of horizontal and oblique image motion. They are, however, influenced neither by pure vertical stimulus movement nor by eye movements in the dark. Electrical stimulation of the NOT-DTN leads to pure horizontal optokinetic nystagmus with ipsiversive slow phases and does not influence vertical eye position. In addition, unilateral reversible inactivation of the NOT-DTN with muscimol elicits spontaneous contraversive horizontal nystagmus without vertical component. During oblique optokinetic stimulation, the ipsiversive OKN component is significantly decreased in all directions. After bilateral NOT-DTN inactivation, OKN can only be elicited in a narrow range of upward directions. These data indicate that the NOT-DTN is the only source to drive the horizontal component of OKN.

Effects on the optokinetic system of midline lesions in the pretectum of monkeys

The nucleus of the optic tract (NOT), an important visuo-motor relay between the retina and preoculomotor structures, is responsible for mediating horizontal optokinetic nystagmus (OKN) in monkeys, cats, rabbits and rats. In addition to its projection to the vestibular nuclei, the NOT has a prominent projection to the contralateral NOT via the posterior commissure. In order to evaluate the role of the commissural fibers between the NOTs in OKN, we cut the posterior commissure in three Macaca fuscata. The animals viewed the OKN stripes under three conditions: right eye viewing, left eye viewing, and both eyes viewing. OKN was recorded in response to counter-clockwise and clockwise stimulation at stimulus velocities of 30 degrees/s, 60 degrees/s and 90 degrees/s. After control data were gathered, the posterior commissure was transected with an operating knife. Before the animal was sacrificed, biocytin, an anterograde tracer, was injected into the left NOT in order to confirm that all of the commissural fibers had been cut. Although the midline lesions decreased the initial rapid rise and steady state OKN slow-phase velocity in all three animals, there were no directional differences observed during monocular clockwise or counter-clockwise visual stimulation to either eye. In two of the three animals, there were no significant differences in the time-constants of optokinetic after nystagmus (OKAN) after the lesion. In the remaining animal, the time-constants decreased at stimulus velocities of 30 degrees/s and 60 degrees/s. In conclusion, gain reduction in the rapid rise and steady state slow-phase velocity of OKN can be explained by removal of an excitatory signal mediated by commissural fibers to inhibitory interneurons in the contralateral NOT. However, interrupting the commissural fibers had no effect on the velocity storage mechanism, because the time-constants of OKAN mostly remained largely unchanged by the lesion.