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First published online on November 8, 2002.
Copyright © 2002 by The Physiological Society
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2002.027797v1
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Received July 1, 2002
Accepted after revision October 7, 2002

Firing behaviour of squirrel monkey eye-movement related vestibular nucleus neurons during gaze saccades

R. A. McCrea1* and Greg T. Gdowski2

1 Dept. of Neurobiology, Pharmacology and Physiology, University of Chicago, 5806 S. Ellis Avenue, Chicago, Illinois 60637, USA
2 Department of Neurobiology, Pharmacology and Physiology, Committee on Neurobiology, University of Chicago, 5806 South Ellis Avenue, Chicago, Illinois 60637, USA

* To whom correspondence should be addressed. E-mail: ramccrea{at}midway.uchicago.edu.

The firing behavior of vestibular nucleus neurons putatively involved in producing the vestibulo-ocular reflex (VOR) was studied during active and passive head movements in squirrel monkeys. Single unit recordings were obtained from 14 position-vestibular (PV) neurons, 30 position-vestibular-pause (PVP) neurons and eight eye-head-vestibular (EHV) neurons. Neurons were sub-classified as type I or II based on whether they were excited or inhibited during ipsilateral head rotation. Different classes of cell exhibited distinctive responses during active head movements produced during and after gaze saccades. Type I PV cells were nearly as sensitive to active head movements as they were to passive head movements during saccades. Type II PV neurons were insensitive to active head movements both during and after gaze saccades. PVP and EHV neurons were insensitive to active head movements during saccadic gaze shifts, and exhibited asymmetric sensitivity to active head movements following the gaze shift. PVP neurons were less sensitive to on direction head movements during the VOR after gaze saccades, while EHV neurons exhibited an enhanced sensitivity to head movements in their on direction. Vestibular signals related to the passive head movement were faithfully encoded by VN neurons. We conclude that central VOR pathway neurons are differentially sensitive to active and passive head movements both during and after gaze saccades due primarily to an input related to head movement motor commands. The convergence of motor and sensory reafferent inputs on VOR pathways provides a mechanism for separate control of eye and head movements during and after saccadic gaze shifts.




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