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The Journal of Neurophysiology Vol. 82 No. 6 December 1999, pp. 3254-3267
Copyright ©1999 by the American Physiological Society
1Graduate Group in Bioengineering, University of California, San Francisco 94143; 2Graduate Group in Bioengineering, University of California, Berkeley 94720; and 3The Smith-Kettlewell Eye Research Institute, San Francisco, California 94115
Gandhi, Neeraj J. and
Edward L. Keller.
Activity of the Brain Stem Omnipause Neurons During Saccades
Perturbed by Stimulation of the Primate Superior Colliculus. J. Neurophysiol. 82: 3254-3267, 1999. Stimulation
of the rostral ~2 mm of the superior colliculus (SC) during a large,
visual target-initiated saccade produces a spatial deviation of the
ongoing saccade and then stops it in midflight. After the termination
of the stimulation, the saccade resumes and ends near the location of
the flashed target. The density of collicular projections to the
omnipause neuron (OPN) region is greatest from the rostral SC and
decreases gradually for the more caudal regions. It has been
hypothesized that the microstimulation excites the OPNs through these
direct connections, and the reactivation of OPNs, which are normally
silent during saccades, stops the initial component in midflight by
gating off the saccadic burst generator. Two predictions emerge from
this hypothesis: 1) for microstimulation triggered on the
onset of large saccades, the time from stimulation onset to resumption of OPN discharge should decrease as the stimulation site is moved rostral and 2) the lead time from reactivation of OPNs to
the end of the initial saccade on stimulation trials should be equal to
the lead time of pause end with respect to the end of control saccades.
We tested this hypothesis by recording OPN activity during saccades
perturbed by stimulation of the rostral ~2 mm of the SC. The distance
of the stimulation site from the most rostral extent of the SC and the
time of reactivation with respect to stimulation onset were not
significantly correlated. The mean lead of reactivation of OPNs
relative to the end of the initial component of perturbed saccades (6.5 ms) was significantly less than the mean lead with respect to the
end of control (9.6 ms) and resumed saccades (10.4 ms). These results
do not support the notion that the excitatory input from SC neurons
in
particular, the fixation neurons in the rostral SC
provide the major
signal to reactivate OPNs and end saccades. An alternative, conceptual model to explain the temporal sequence of events induced by stimulation of the SC during large saccades is presented. Other OPN activity parameters also were measured and compared for control and stimulation conditions. The onset of pause with respect to resumed saccade onset
was larger and more variable than the onset of pause with respect to
control saccades, whereas pause end with respect to the end of resumed
and control saccades was similar. The reactivated discharge of OPNs
during the period between the end of the initial and the onset of the
resumed saccades was at least as strong as that following control
movements. This latter observation is interpreted in terms of the
resettable neural integrator hypothesis.
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