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The Journal of Neurophysiology Vol. 87 No. 2 February 2002, pp. 912-924
Copyright ©2002 by the American Physiological Society
1Department of Neurology, Medical University of Lübeck, 23538 Lubeck, Germany; and 2Howard Hughes Medical Institute, W. M. Keck Foundation Center of Integrative Neuroscience, Department of Physiology, and 3Department of Neurological Surgery, University of California, San Francisco, California 94143
Rambold, H.,
A. Churchland,
Y. Selig,
L. Jasmin, and
S. G. Lisberger.
Partial Ablations of the Flocculus and Ventral Paraflocculus in
Monkeys Cause Linked Deficits in Smooth Pursuit Eye Movements and
Adaptive Modification of the VOR. J. Neurophysiol. 87: 912-924, 2002. The vestibuloocular reflex
(VOR) generates compensatory eye movements to stabilize visual images
on the retina during head movements. The amplitude of the reflex is
calibrated continuously throughout life and undergoes adaptation, also
called motor learning, when head movements are persistently associated
with image motion. Although the floccular-complex of the cerebellum is
necessary for VOR adaptation, it is not known whether this function is
localized in its anterior or posterior portions, which comprise the
ventral paraflocculus and flocculus, respectively. The present paper
reports the effects of partial lesions of the floccular-complex in five macaque monkeys, made either surgically or with stereotaxic injection of 3-nitropropionic acid (3-NP). Before and after the lesions, smooth
pursuit eye movements were tested during sinusoidal and step-ramp
target motion. Cancellation of the VOR was tested by moving a target
exactly with the monkey during sinusoidal head rotation. The control
VOR was tested during sinusoidal head rotation in the dark and during
30°/s pulses of head velocity. VOR adaptation was studied by having
the monkeys wear ×2 or ×0.25 optics for 4-7 days. In two monkeys,
bilateral lesions removed all of the flocculus except for parts of
folia 1 and 2 but did not produce any deficits in smooth pursuit, VOR
adaptation, or VOR cancellation. We conclude that the flocculus alone
probably is not necessary for either pursuit or VOR learning. In two
monkeys, unilateral lesions including a large fraction of the ventral
paraflocculus produced small deficits in horizontal and vertical smooth
pursuit, and mild impairments of VOR adaptation and VOR cancellation.
We conclude that the ventral paraflocculus contributes to both
behaviors. In one monkey, a bilateral lesion of the flocculus and
ventral paraflocculus produced severe deficits smooth pursuit and VOR cancellation, and a complete loss of VOR adaptation. Considering all
five cases together, there was a strong correlation between the size of
the deficits in VOR learning and pursuit. We found the strongest
correlation between the behavior deficits and the size of the lesion of
the ventral paraflocculus, a weaker but significant correlation for the
full floccular complex, and no correlation with the size of the lesion
of the flocculus. We conclude that 1) lesions of the
floccular complex cause linked deficits in smooth pursuit and VOR
adaptation, and 2) the relevant portions of the structure
are primarily in the ventral paraflocculus, although the flocculus may participate.
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