Mingxia Zhu

Vergence nystagmus induced by motion in the ground plane: normal response characteristics.

We displayed backward/forward motion on a computer monitor in the ground plane. Subjects looked at the center of a moving pattern and eye movements of both eyes were recorded with a search coil system. Involuntary nystagmus including vertical version (VV) and horizontal vergence (HV) was recorded. Dynamics of the nystagmus showed that the slow and quick phase of VV and HV were always associated with each other while the monocular horizontal eye movements composed of HV were either symmetrical or asymmetrical. Peak velocity, amplitudes and frequency of the VV and HV responses were quantified. The results suggest that involuntary HV nystagmus can be induced by simple motion from simulated optic flow in the ground plane and the HV nystagmus helps moving subjects to stabilize their gazes on the object of interest.

Relationships between versional and vergent quick phases of the involuntary version-vergence nystagmus.

We used ground-plane motion stimuli displayed on a computer monitor positioned below eye level to induce involuntary version-vergence nystagmus (VVN). The VVN was recorded with a search coil system. It was shown that the VVN had both vertical versional and horizontal vergence components. The VVN induced by backward motion (toward subjects) had upward versional and divergence quick phases, whereas those induced by forward motion (away from subjects) had downward and biphasic divergence-convergence quick phases. The versional and vergence components of the VVN quick phases were analyzed. A temporal dissociation of about 20 ms between version velocity peak and convergence velocity peak was revealed, which supported a modified saccade-related vergence burst neuron (SVBN) model. We suggest that the temporal dissociation may be partly because of a lower-level OKN control mechanism. Vergence peak time was dependent on version peak time. Linear relationships between vergence peak velocity and versional saccadic peak velocity were demonstrated, which was in line with the new multiplicative model. Our data support the hypothesis that the vergence system and the saccadic system can act separately but interact with each other whenever their movements occur simultaneously.

Effect of binocular rivalry suppression on initial ocular following responses.

To study the effect of binocular rivalry (BR) suppression on the ocular following response (OFR), we recorded the OFR in both the suppressed and the dominant phases of BR. The BR was established using stationary horizontal/vertical grating patterns presented on two PC monitors. Once a subjective image of a vertical or horizontal grating pattern was perceived, subjects pressed a button to trigger an onset of brief horizontal movement (750 ms) of the vertical grating pattern and an offset of the horizontal pattern. The OFRs were recorded using a scleral search coil system at 1 kHz. The OFRs from the suppressed phases were significantly reduced compared to those from the dominant phases. The OFRs were asymmetrical to temporalward and nasalward motion in most conditions. We suggest that asymmetry of OFRs under the incomplete BR conditions may be a reflection of imbalance binocular inputs and processing in the visual system similar to asymmetrical optokinetic nystagmus in strabismic subjects. The latency of the OFR in deeper suppressed conditions was prolonged, suggesting that the interaction of BR and OFR may occur at multiple stages including an early stage of the visual processing. The OFR may have the potential for objective measurement of BR suppression in clinical evaluation of binocular function.

Effect of Artificial Scotomas on Open-loop Disparity Vergence Eye Movements

Purpose To investigate the effect of an artificial scotoma on open-loop disparity vergence responses (DVRs) and vergence control mechanisms, we examined open-loop DVRs to disparity stimuli using monocular artificial scotomas in normal subjects. Methods Using a mirror haploscope with two computer monitors, we delivered disparity stimuli on a pair of random dot patterns subtending 40 by 30 degrees at 47 cm from each eye. The scotomas were black circles located in the center of a random dot pattern for the left eye. Eye movements of both eyes were recorded with a magnetic search coil system. Results We first found that the amplitudes of DVRs were gradually decreased and the latency of DVRs was moderately increased as the size of the scotomas was increased. Second, monocular responses from each eye were symmetrical although the stimuli to each eye were asymmetrical. Conclusions The results suggest that the monocular eye movements in disparity vergence are controlled by a binocular central mechanism, not driven separately by monocular inputs in the open-loop window.