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The Journal of Neurophysiology Vol. 82 No. 1 July 1999, pp. 436-449
Copyright ©1999 by the American Physiological Society
Department of Neurobiology, Pharmacology, and Physiology, University of Chicago, Chicago, Illinois 60637
Gdowski, Greg T. and
Robert A. McCrea.
Integration of Vestibular and Head Movement Signals in the
Vestibular Nuclei During Whole-Body Rotation. J. Neurophysiol. 82: 436-449, 1999.
Single-unit recordings were obtained from 107 horizontal semicircular canal-related central vestibular neurons in
three alert squirrel monkeys during passive sinusoidal whole-body
rotation (WBR) while the head was free to move in the yaw plane (2.3 Hz, 20°/s). Most of the units were identified as secondary vestibular neurons by electrical stimulation of the ipsilateral vestibular nerve
(61/80 tested). Both non-eye-movement (n = 52) and
eye-movement-related (n = 55) units were studied. Unit
responses recorded when the head was free to move were compared with
responses recorded when the head was restrained from moving. WBR in the
absence of a visual target evoked a compensatory vestibulocollic reflex
(VCR) that effectively reduced the head velocity in space by an average
of 33 ± 14%. In 73 units, the compensatory head movements were
sufficiently large to permit the effect of the VCR on vestibular signal
processing to be assessed quantitatively. The VCR affected the
rotational responses of different vestibular neurons in different ways.
Approximately one-half of the units (34/73, 47%) had responses that
decreased as head velocity decreased. However, the responses of many
other units (24/73) showed little change. These cells had signals that were better correlated with trunk velocity than with head velocity. The
remaining units had responses that were significantly larger (15/73,
21%) when the VCR produced a decrease in head velocity. Eye-movement-related units tended to have rotational responses that
were correlated with head velocity. On the other hand,
non-eye-movement units tended to have rotational responses that were
better correlated with trunk velocity. We conclude that sensory
vestibular signals are transformed from head-in-space coordinates to
trunk-in-space coordinates on many secondary vestibular neurons in the
vestibular nuclei by the addition of inputs related to head rotation on
the trunk. This coordinate transformation is presumably important for
controlling postural reflexes and constructing a central percept of
body orientation and movement in space.
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