The Journal of Neurophysiology Vol. 81 No. 5 May 1999, pp. 2119-2130
Copyright ©1999 by the American Physiological Society

Short- and Long-Term Consequences of Canal Plugging on Gaze Shifts in the Rhesus Monkey. I. Effects on Gaze Stabilization

 ¹Department of Surgery (Otolaryngology), University of Mississippi Medical Center, Jackson, Mississippi 39212;  ²Regional Primate Research Center,  ³Department of Physiology and Biophysics, and  ⁴Department of Otolaryngology, Head and Neck Surgery, University of Washington, Seattle, Washington 98195; and  ⁵Department of Neurology, Center for Sensorimotor Research, Ludwig Maximilians University, D81377 Munich, Germany

Newlands, Shawn D., Leo Ling, James O. Phillips, Christoph Siebold, Larry Duckert, and Albert F. Fuchs. Short- and Long-Term Consequences of Canal Plugging on Gaze Shifts in the Rhesus Monkey. I. Effects on Gaze Stabilization. J. Neurophysiol. 81: 2119-2130, 1999.Short- and long-term consequences of canal plugging on gaze shifts in the rhesus monkey. I. Effects on gaze stabilization. To study the contribution of the vestibular system to the coordinated eye and head movements of a gaze shift, we plugged the lumens of just the horizontal (n = 2) or all six semicircular canals (n = 1) in monkeys trained to make horizontal head-unrestrained gaze shifts to visual targets. After the initial eye saccade of a gaze shift, normal monkeys exhibit a compensatory eye counterrotation that stabilizes gaze as the head movement continues. This counterrotation, which has a gain (eye velocity/head velocity) near one has been attributed to the vestibuloocular reflex (VOR). One day after horizontal canal plugging, the gain of the passive horizontal VOR at frequencies between 0.1 and 1.0 Hz was <0.10 in the horizontal-canal-plugged animals and zero in the all-canal-plugged animal. One day after surgery, counterrotation gain was ~0.3 in the animals with horizontal canals plugged and absent in the animal with all canals plugged. As the time after plugging increased, so too did counterrotation gain. In all three animals, counterrotation gain recovered to between 0.56 and 0.75 within 80-100 days. The initial loss of compensatory counterrotation after plugging resulted in a gaze shift that ended long after the eye saccade and just before the end of the head movement. With recovery, the length of time between the end of the eye saccade and the end of the gaze movement decreased. This shortening of the duration of reduced gain counterrotation occurred both because head movements ended sooner and counterrotation gain returned to 1.0 more rapidly relative to the end of the eye saccade. Eye counterrotation was not due to activation of pursuit eye movements as it persisted when gaze shifts were executed to extinguished targets. Also counterrotation was not due simply to activation of neck receptors because counterrotation persisted after head movements were arrested in midflight. We suggest that the neural signal that is used to cause counterrotation in the absence of vestibular input is an internal copy of the intended head movement.