Literature DB >> 8930270

Modulation of the human vestibuloocular reflex during saccades: probing by high-frequency oscillation and torque pulses of the head.

S Tabak1, J B Smeets, H Collewijn.   

Abstract

1. We probed the gain and phase of the vestibuloocular reflex (VOR) during the execution of voluntary gaze saccades, with continuous oscillation or acceleration pulses, applied through a torque helmet. 2. Small-amplitude (< 1 degree), high-frequency (10-14 Hz) head oscillations in the horizontal or vertical plane were superimposed on ongoing horizontal gaze saccades (40-100 degrees). Torque pulses to the head ("with" or "against" gaze) were superimposed on 40 degrees horizontal saccades. Eye and head movements were precisely measured with sensor coils in magnetic fields. 3. Techniques were developed to separate the oscillatory (horizontal or vertical) component from the gaze shift and obtain VOR gain and phase with Fourier techniques from the relation between eye-in-head and head oscillations. These involved either subtraction of exactly matching saccades with and without oscillation (drawback: low yield) or time shifting of successive trials to synchronize the oscillations (drawback: slight time blurring of saccades). 4. The results of these matching and synchronization methods were essentially identical and consistent. Presaccadic gain values of the horizontal VOR (typically about unity) were reduced by, on average, approximately 20 and 50% during horizontal saccades of 40 and 100 degrees, respectively. These percentages may be truncated because of methodological limitations, but even after taking these into account (on the basis of simulation experiments with 2 different, theoretical profiles of suppression) our results do not support a complete saccadic VOR suppression for any substantial fraction of saccadic duration. Qualitatively similar changes were found when the vertical VOR was probed during 100 degrees horizontal saccades. 5. Concomitantly with the reductions in gain, VOR phase was advanced by approximately 20 degrees during the saccade. 6. In the wake of gaze saccades, VOR gain was consistently elevated (to approximately 1.0) above the presaccadic level (approximately 0.9). We submit that this mechanism ensures stable fixation of the newly acquired target at a time when the head is still moving substantially. 7. Although the responses to head torque pulses showed idiosyncratic asymmetries, analysis of the differences in eye and head movements for pulses with and against consistently showed a sharp fall of VOR gain at saccadic onset, following an approximately exponential course with a time constant of approximately 50 ms. This decay may be assumed to reflect VOR gain for a period of approximately 50 ms, after which secondary gaze control mechanisms become dominant. 8. The time course of the gain decay and phase shift of the VOR suggest that suppression of the "integrative (position) loop" of the VOR circuit was more complete than suppression of the direct, "velocity" pathway.

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Year:  1996        PMID: 8930270     DOI: 10.1152/jn.1996.76.5.3249

Source DB:  PubMed          Journal:  J Neurophysiol        ISSN: 0022-3077            Impact factor:   2.714


  16 in total

1.  Electrical stimulation of rhesus monkey nucleus reticularis gigantocellularis. II. Effects on metrics and kinematics of ongoing gaze shifts to visual targets.

Authors:  Edward G Freedman; Stephan Quessy
Journal:  Exp Brain Res       Date:  2004-02-21       Impact factor: 1.972

2.  Matching the oculomotor drive during head-restrained and head-unrestrained gaze shifts in monkey.

Authors:  Bernard P Bechara; Neeraj J Gandhi
Journal:  J Neurophysiol       Date:  2010-05-26       Impact factor: 2.714

3.  Kinematics and eye-head coordination of gaze shifts evoked from different sites in the superior colliculus of the cat.

Authors:  Alain Guillaume; Denis Pélisson
Journal:  J Physiol       Date:  2006-10-05       Impact factor: 5.182

4.  Coupling between horizontal and vertical components of saccadic eye movements during constant amplitude and direction gaze shifts in the rhesus monkey.

Authors:  Edward G Freedman
Journal:  J Neurophysiol       Date:  2008-10-22       Impact factor: 2.714

5.  Gaze pursuit responses in nucleus reticularis tegmenti pontis of head-unrestrained macaques.

Authors:  David A Suzuki; Kathleen F Betelak; Robert D Yee
Journal:  J Neurophysiol       Date:  2008-11-05       Impact factor: 2.714

6.  Gaze shifts to auditory and visual stimuli in cats.

Authors:  Janet L Ruhland; Tom C T Yin; Daniel J Tollin
Journal:  J Assoc Res Otolaryngol       Date:  2013-06-08

7.  Coordination of eye and head components of movements evoked by stimulation of the paramedian pontine reticular formation.

Authors:  Neeraj J Gandhi; Ellen J Barton; David L Sparks
Journal:  Exp Brain Res       Date:  2008-05-06       Impact factor: 1.972

8.  Kinematic synergies during saccades involving whole-body rotation: a study based on the uncontrolled manifold hypothesis.

Authors:  Adriana M Degani; Alessander Danna-Dos-Santos; Thomas Robert; Mark L Latash
Journal:  Hum Mov Sci       Date:  2010-03-25       Impact factor: 2.161

9.  Vestibulo-ocular reflex suppression during head-fixed saccades reveals gaze feedback control.

Authors:  Pierre M Daye; Dale C Roberts; David S Zee; Lance M Optican
Journal:  J Neurosci       Date:  2015-01-21       Impact factor: 6.167

Review 10.  Vestibular control of the head: possible functions of the vestibulocollic reflex.

Authors:  Jay M Goldberg; Kathleen E Cullen
Journal:  Exp Brain Res       Date:  2011-03-26       Impact factor: 1.972

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