Endpoint accuracy in saccades interrupted by stimulation in the omnipause region in monkey

Electrical stimulation of the omnipause neuron region (OPN) at saccade onset results in interrupted saccades (IS)- eye movements which pause in midflight, resume after a brief period, and end near the target location. Details on the endpoint accuracy of IS do not exist, except for a brief report by Becker et al. (1981). Their analysis emphasized the accuracy of IS relative to the visual target which remained on during the interrupted period. We instead quantified the metric properties of IS relative to nonstimulated saccades during a target flash paradigm. Our results show that IS tend to be slightly hypermetric relative to the nonstimulated saccades to the same target location. The amount of overshoot is not correlated with target eccentricity. Detailed analyses also indicate that the standard deviations of the endpoint in IS are not significantly larger than those for nonstimulated saccades, although there was a much larger variability produced in eye position during the interruption. Both these latter observations support the notion that saccades are controlled by an internal negative feedback system. Also, the size of the remaining motor error during the interrupted period is one factor influencing when an IS resumes, but the variability in this measure is large particularly for smaller motor errors. Recent results have suggested that the resettable neural integrator involved in the feedback loop may be reset after each saccade through an exponential decay process. To probe the properties of the neural integrator, we varied the duration of interruption between the initial and resumed saccades and sought a systematic overshoot in the final eye position with increasing interruption period and variable initial saccade size. Our results showed the neural integrator does not decay during the pause period of interrupted saccades.

[1]  D. Robinson Eye movements evoked by collicular stimulation in the alert monkey. , 1972, Vision research.

[2]  C. Scudder A new local feedback model of the saccadic burst generator. , 1988, Journal of neurophysiology.

[3]  B. Richmond,et al.  Implantation of magnetic search coils for measurement of eye position: An improved method , 1980, Vision Research.

[4]  D. Robinson,et al.  A METHOD OF MEASURING EYE MOVEMENT USING A SCLERAL SEARCH COIL IN A MAGNETIC FIELD. , 1963, IEEE transactions on bio-medical engineering.

[5]  S. Highstein,et al.  The anatomy and physiology of primate neurons that control rapid eye movements. , 1994, Annual review of neuroscience.

[6]  A. Fuchs,et al.  A method for measuring horizontal and vertical eye movement chronically in the monkey. , 1966, Journal of applied physiology.

[7]  E. Keller,et al.  Visual and oculomotor signals in nucleus reticularis tegmenti pontis in alert monkey. , 1985, Journal of neurophysiology.

[8]  E. Keller Participation of medial pontine reticular formation in eye movement generation in monkey. , 1974, Journal of neurophysiology.

[9]  R. Wurtz,et al.  Fixation cells in monkey superior colliculus. II. Reversible activation and deactivation. , 1993, Journal of neurophysiology.

[10]  M. J. Nichols,et al.  Nonstationary properties of the saccadic system: new constraints on models of saccadic control. , 1995, Journal of neurophysiology.

[11]  D L Robinson,et al.  Modified saccades evoked by stimulation of the macaque superior colliculus account for properties of the resettable integrator. , 1995, Journal of neurophysiology.

[12]  M. Sanders Control of Gaze by Brain Stem Neurons , 1978 .

[13]  E. Keller,et al.  Use of interrupted saccade paradigm to study spatial and temporal dynamics of saccadic burst cells in superior colliculus in monkey. , 1994, Journal of neurophysiology.

[14]  S. Gielen,et al.  A quantitative analysis of generation of saccadic eye movements by burst neurons. , 1981, Journal of neurophysiology.