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The Journal of Neurophysiology Vol. 88 No. 3 September 2002, pp. 1234-1244
Copyright ©2002 by the American Physiological Society
Departments of 1Neurobiology, Pharmacology, and Physiology and 2Surgery (Otolaryngology-Head and Neck Surgery), University of Chicago, Chicago, Illinois 60637
Plotnik, Meir,
Vladimir Marlinski, and
Jay
M. Goldberg.
Reflections of Efferent Activity in Rotational Responses of
Chinchilla Vestibular Afferents. J. Neurophysiol. 88: 1234-1244, 2002. To study presumed
efferent-mediated responses, we determined if afferents responded to
head rotations that stimulated semicircular canals other than the organ
being innervated. To minimize stimulation of an afferent's own canal,
its plane was placed nearly orthogonal to the rotation plane. Otolith
units were tested in a horizontal head position with the ear placed
near the rotation axis to minimize linear forces. Under these
circumstances, angular-velocity trapezoids (2-s ramps, 2-s plateau)
evoked excitatory responses for both rotation directions. These type
III responses were considerably larger in decerebrate than in
anesthetized preparations. In addition to their being exclusively
excitatory, the responses resembled those obtained with electrical
stimulation of efferent pathways in including per-stimulus and more
prolonged post-stimulus components and in being larger in irregularly
discharging than in regularly discharging units. Responses, which were
not seen for rotations <80°/s, grew as velocity increased between 80 and 500°/s but were seldom larger than 20 spikes/s. Complete section
of the VIIIth nerve abolished type III responses, leaving conventional
afferent responses intact. To study the separate contributions of
canals on the two sides, responses were compared when the labyrinths were intact and when the ipsilateral or contralateral horizontal canal
was mechanically inactivated. Both sides contributed to the
efferent-mediated responses. That afferents could be influenced from
the contralateral labyrinth was confirmed with the use of unilateral
galvanic currents. Following inactivation, excitatory responses were
produced by rotations exciting or inhibiting the intact horizontal
canal with the responses resulting from excitatory rotations being much
larger. Such a response asymmetry is consistent with a
semicircular-canal origin for the type III responses. A similar
asymmetry was seen in the post-stimulus responses to contralateral cathodal (excitatory) and anodal (inhibitory) galvanic currents. We
conclude that the efferent system receives a sufficiently powerful vestibular input from both the ipsilateral and contralateral labyrinths to affect afferent discharge.
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