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The Journal of Neurophysiology Vol. 88 No. 4 October 2002, pp. 1726-1742
Copyright ©2002 by the American Physiological Society
Department of Neurology and Neurosurgery, and Montreal Neurological Institute, McGill University, Montreal, Quebec H3A 2B4, Canada
Bergeron, André and
Daniel Guitton.
In Multiple-Step Gaze Shifts: Omnipause (OPNs) and Collicular
Fixation Neurons Encode Gaze Position Error; OPNs Gate Saccades. J. Neurophysiol. 88: 1726-1742, 2002. The superior colliculus (SC), via
its projections to the pons, is a critical structure for driving rapid
orienting movements of the visual axis, called gaze saccades, composed
of coordinated eye-head movements. The SC contains a motor map that
encodes small saccade vectors rostrally and large ones caudally. A zone
in the rostral pole may have a different function. It contains superior colliculus fixation neurons (SCFNs) with probable projections to
omnipause neurons (OPNs) of the pons. SCFNs and OPNs discharge tonically during visual fixation and pause during single-step gaze
saccades. The OPN tonic discharge inhibits saccades and its cessation
(pause) permits saccade generation. We have proposed that SCFNs control
the OPN discharge. We compared the discharges of SCFNs and OPNs
recorded while cats oriented horizontally, to the left and right, in
the dark to a remembered target. Cats used multiple-step gaze shifts
composed of a series of small gaze saccades, of variable amplitude and
number, separated by periods of variable duration (plateaus) in which
gaze was immobile or moving at low velocity (<25°/s). Just after
contralaterally (ipsilaterally) presented targets, the firing frequency
of SCFNs decreased to almost zero (remained constant at background). As
multiple-step gaze shifts progressed in either direction in the dark,
these activity levels prevailed until the distance between gaze and target [gaze position error (GPE)] reached ~16°. At this point, firing frequency gradually increased, without saccade-related pauses,
until a maximum was reached when gaze arrived on target location
(GPE = 0°). SCFN firing frequency encoded GPE; activity was not
correlated to characteristics or occurrence of gaze saccades. By
comparison, after target presentation to left or right, OPN activity
remained steady at pretarget background until first gaze saccade onset,
during which activity paused. During the first plateau, activity
resumed at a level lower than background and continued at this level
during subsequent plateaus until GPE ~8° was reached. As GPE
decreased further, tonic activity during plateaus gradually increased
until a maximum (greater than background) was reached when gaze was on
goal (GPE = 0°). OPNs, like SCFNs, encoded GPE, but they paused
during every gaze saccade, thereby revealing, unlike for SCFNs, strong
coupling to motor events. The firing frequency increase in SCFNs as GPE
decreased, irrespective of trajectory characteristics, implies these
cells get feedback on GPE, which they may communicate to OPNs. We
hypothesize that at the end of a gaze-step sequence, impulses from
SCFNs onto OPNs may suppress further movements away from the target.
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