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Head Position Modulates Optokinetic Nystagmus

Overview
Journal Exp Brain Res
Specialty Neurology
Date 2011 Jul 8
PMID 21735244
Citations 2
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Abstract

Orientation and movement relies on both visual and vestibular information mapped in separate coordinate systems. Here, we examine how coordinate systems interact to guide eye movements of rabbits. We exposed rabbits to continuous horizontal optokinetic stimulation (HOKS) at 5°/s to evoke horizontal eye movements, while they were statically or dynamically roll-tilted about the longitudinal axis. During monocular or binocular HOKS, when the rabbit was roll-tilted 30° onto the side of the eye stimulated in the posterior → anterior (P → A) direction, slow phase eye velocity (SPEV) increased by 3.5-5°/s. When the rabbit was roll-tilted 30° onto the side of the eye stimulated in the A → P direction, SPEV decreased to ~2.5°/s. We also tested the effect of roll-tilt after prolonged optokinetic stimulation had induced a negative optokinetic afternystagmus (OKAN II). In this condition, the SPEV occurred in the dark, "open loop." Modulation of SPEV of OKAN II depended on the direction of the nystagmus and was consistent with that observed during "closed loop" HOKS. Dynamic roll-tilt influenced SPEV evoked by HOKS in a similar way. The amplitude and the phase of SPEV depended on the frequency of vestibular oscillation and on HOKS velocity. We conclude that the change in the linear acceleration of the gravity vector with respect to the head during roll-tilt modulates the gain of SPEV depending on its direction. This modulation improves gaze stability at different image retinal slip velocities caused by head roll-tilt during centric or eccentric head movement.

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References
1.
Pettorossi V, Errico P, Santarelli R . Contribution of the maculo-ocular reflex to gaze stability in the rabbit. Exp Brain Res. 1991; 83(2):366-74. DOI: 10.1007/BF00231160. View

2.
Barmack N, Nelson B . Influence of long-term optokinetic stimulation on eye movements of the rabbit. Brain Res. 1987; 437(1):111-20. DOI: 10.1016/0006-8993(87)91532-0. View

3.
Barmack N, Errico P, Ferraresi A, Fushiki H, Pettorossi V, Yakhnitsa V . Cerebellar nodulectomy impairs spatial memory of vestibular and optokinetic stimulation in rabbits. J Neurophysiol. 2002; 87(2):962-75. DOI: 10.1152/jn.00528.2001. View

4.
Curthoys I, Wearne S, Dai M, Halmagyi G, Holden J . Linear acceleration modulates the nystagmus induced by angular acceleration stimulation of the horizontal canal. Ann N Y Acad Sci. 1992; 656:716-24. DOI: 10.1111/j.1749-6632.1992.tb25249.x. View

5.
Clement G . A review of the effects of space flight on the asymmetry of vertical optokinetic and vestibulo-ocular reflexes. J Vestib Res. 2004; 13(4-6):255-63. View