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Abstract
Off-vertical rotation (OVAR) in darkness induced continuous horizontal nystagmus in
humans at small tilts of the rotation axis (5 to 30 degrees). The horizontal slow
eye velocity had two components: a mean velocity in the direction opposite to head
rotation and a sinusoidal modulation around the mean. Mean velocity generally did
not exceed 10 deg/s, and was less than or equal to the maximum velocity of optokinetic
after-nystagmus (OKAN). Both the mean and modulation components of horizontal nystagmus
increased with tilt angle and rotational velocity. Vertical slow eye velocity was
also modulated sinusoidally, generally around zero. The amplitude of the vertical
modulation increased with tilt angle, but not with rotational velocity. In addition
to modulations in eye velocity, there were also modulations in horizontal and vertical
eye positions. These would partially compensate for head position changes in the yaw
and pitch planes during each cycle of OVAR. Modulations in vertical eye position were
regular, increased with increases in tilt angle and were separated from eye velocity
by 90 deg. These results are compatible with the interpretation that, during OVAR,
mean slow velocity of horizontal nystagmus is produced by the velocity storage mechanism
in the vestibular system. In addition, they indicate that the otolith organs induce
compensatory eye position changes with regard to gravity for tilts in the pitch, yaw
and probably also the roll planes. Such compensatory changes could be utilized to
study the function of the otolith organs. A functional interpretation of these results
is that nystagmus attempts to stabilize the image on the retina of one point of the
surrounding world. Mean horizontal velocity would then be opposite to the estimate
of head rotational velocity provided by the output of the velocity storage mechanism,
as charged by an otolithic input during OVAR. In spite of the lack of actual translation,
an estimate of head translational velocity could, in this condition, be constructed
from the otolithic signal. The modulation in horizontal eye position would then be
compensatory for the perceived head translation. Modulation of vertical eye velocity
would compensate for actual changes in head orientation with respect to gravity.
Vestibular and optokinetic nystagmus (OKN) of monkeys were induced by platform and visual surround rotation. Vision prolonged per-rotatory nystagmus and cancelled or reduced post-rotatory nystagmus recorded in darkness. Presumably, activity stored during OKN summed with activity arising in the semicircular canals. The limit of summation was about 120 degrees/s, the level of saturation of optokinetic after-nystagmus (OKAN). OKN and vestibular nystagmus, induced in the same or in opposite directions diminished or enhanced post-rotatory nystagmus up to 120 degrees/s. We postulate that a common storage mechanism is used for producing vestibular nystagmus, OKN, and OKAN. Evidence for this is the similar time course of vestibular nystagmus and OKAN and their summation. In addition, stored activity is lost in a similar way by viewing a stationary surround during either OKAN or vestibular nystagmus (fixation suppression). These responses were modelled using direct pathways and a non-ideal integrator coupled to the visual and peripheral vestibular systems. The direct pathways are responsible for rapid changes in eye velocity while the integrator stores activity and mediates slower changes. The integrator stabilizes eye velocity during whole field rotation and extends the time over which the vestibulo-ocular reflex can compensate for head movement.
Gaze, the direction of the visual axis in space, is the sum of the eye position relative to the head (E) plus head position relative to space (H). In the old explanation, which we call the oculocentric motor strategy, of how a rapid orienting gaze shift is controlled, it is assumed that 1) a saccadic eye movement is programmed with an amplitude equal to the target's offset angle, 2) this eye movement is programmed without reference to whether a head movement is planned, 3) if the head turns simultaneously the saccade is reduced in size by an amount equal to the head's contribution, and 4) the saccade is attenuated by the vestibuloocular reflex (VOR) slow phase. Humans have an oculomotor range (OMR) of about +/- 55 degrees. The use of the oculocentric motor strategy to acquire targets lying beyond the OMR requires programming saccades that cannot be made physically. We have studied in normal human subjects rapid horizontal gaze shifts to visible and remembered targets situated within and beyond the OMR at offsets ranging from 30 to 160 degrees. Heads were attached to an apparatus that permitted short unexpected perturbations of the head trajectory. The acceleration and deceleration phases of the head perturbation could be timed to occur at different points in the eye movement. 4. Single-step rapid gaze shifts of all sizes up to at least 160 degrees (the limit studied) could be accomplished with the classic single-eye saccade and an accompanying saccadelike head movement. In gaze shifts less than approximately 45 degrees, when head motion was prevented totally by the brake, the eye attained the target. For larger target eccentricities the gaze shift was interrupted by the brake and the average eye saccade amplitude was approximately 45 degrees, well short of the OMR. Thus saccadic eye movement amplitude was neurally, not mechanically, limited. When the head's motion was not perturbed by the brake, the eye saccade amplitude was a function of head velocity: for a given target offset, the faster the head the smaller the saccade. For gaze shifts to targets beyond the OMR and when head velocity was low, the eye frequently attained the 45 degrees position limit and remained there, immobile, until gaze attained the target.(ABSTRACT TRUNCATED AT 400 WORDS)
1. The directional selectivity of peripheral otolith neurons was studied in the barbiturate-anesthetized squirrel monkey (Saimiri sciureus). Each unit's most sensitive axis was characterized by a functional polarization vector. The direction of a centrifugal force was varied with respect to the vector and to the macular plane. The neurons respond in an excitatory manner to shearing forces orthogonally disposed to the vector. The sensitivity to orthogonal shears was usually 10-15% of the sensitivity to parallel shearing forces. There was no significant response to orthogonal compressions, nor did compressions modify the response to shearing forces. 2. Force-response functions were obtained in the stimulus range of +/- 4.92 g. Forces were directed parallel to each unit's polarization vector. The functions are sigmoid shaped and possess both inhibitory and excitatory plateaus. The presumed physiological range of +/-1 g is represented in the lower (concave upward) portion of the function and has a dynamic range, expressed in terms of response magnitude, amounting to 20-40% of the potential dynamic range of the neuron. 3. There was considerable variation among units in their +/- 4.92 g force-response curves. The salient features of the functions are described by three factors, tentatively identified as a transduction gain, a receptor bias, and a mechanical gain. Both the resting discharge (do) and the +/-1 g sensitivity (so) vary in the same direction with changes in the factors related to transduction gain and receptor bias. It is shown that this covariation provides a quantitatively precise explanation for the positive relation between do and so.
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