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The Journal of Neurophysiology Vol. 83 No. 4 April 2000, pp. 2047-2062
Copyright ©2000 by the American Physiological Society
1Department of Neurology and 2Department of Neurosurgery, The Johns Hopkins Hospital, Baltimore, Maryland 21287; 3Department of Ophthalmology, Niigata University School of Medicine, Niigata 951; and 4Core Research for the Evolutional Science and Technology Program, Japan Science and Technology, Saitama 332-0012, Japan
Takagi, Mineo,
David S. Zee, and
Rafael J. Tamargo.
Effects of Lesions of the Oculomotor Cerebellar Vermis on Eye
Movements in Primate: Smooth Pursuit. J. Neurophysiol. 83: 2047-2062, 2000. We studied the effects on smooth
pursuit eye movements of ablation of the dorsal cerebellar vermis
(lesions centered on lobules VI and VII) in three monkeys in which the
cerebellar nuclei were spared. Following the lesion the latencies to
pursuit initiation were unchanged. Monkeys showed a small decrease (up
to 15%) in gain during triangular-wave tracking. More striking were
changes in the dynamic properties of pursuit as determined in the
open-loop period (the 1st 100 ms) of smooth tracking. Changes included
a decrease in peak eye acceleration (e.g., in one monkey from
~650°/s2, prelesion to ~220-380°/s2,
postlesion) and a decrease in the velocity at the end of the open-loop
period [e.g., in another monkey from a gain (eye velocity/target velocity at 100 ms of tracking) of 0.93, prelesion to 0.53, postlesion]. In individual monkeys, the pattern of deficits in the
open-loop period of pursuit was usually comparable to that of saccades, especially when comparing the changes in the acceleration of pursuit to
the changes in the velocity of saccades. These findings support the
hypothesis that saccades and the open-loop period of pursuit are
controlled by the cerebellar vermis in an analogous way. Saccades could
be generated by eye velocity commands to bring the eyes to a certain
position and pursuit by eye acceleration commands to bring the eyes
toward a certain velocity. On the other hand, changes in gain during
triangular-wave tracking did not correlate with either the saccade or
the open-loop pursuit deficits, implying different contributions of the
oculomotor vermis to the open loop and to the sustained portions of
pursuit tracking. Finally, in a pursuit adaptation paradigm (×0.5 or
×2, calling for a halving or doubling of eye velocity, respectively)
intact animals could adaptively adjust eye acceleration in the
open-loop period. The main pattern of change was a decrease in peak
acceleration for ×0.5 training and an increase in the duration of peak
acceleration for ×2 training. Following the lesion in the oculomotor
vermis, this adaptive capability was impaired. In conclusion, as for
saccades, the oculomotor vermis plays a critical role both in the
immediate on-line and in the short-term adaptive control of pursuit.
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