Literature DB >> 8817276

Eye position and target amplitude effects on human visual saccadic latencies.

J H Fuller1.   

Abstract

Gaze shifts vary in the extent of eye and head contribution; a large amplitude and/or an eccentric ocular orbital starting position alter the participation of head movement in the shift. The interval between eye onset and head onset determines compensatory counterrolling before and after the shift and the extent of vestibular ocular reflex reduction during the shift. The latency of eye saccades in the head-fixed condition was measured with respect to target amplitude and orbital position in order to establish base-line operations of these two variables as they apply to the head-free condition. Eye movements were measured during single-step saccades in nine young adult humans. The target step, hereafter called a jump, started from three possible fixation lights; e.g., rightward saccades started from the midline (0 degree) or from -20 or -40 degrees left of the midline, with a maximum amplitude of 80 degrees. The latency of saccades starting from the primary position increased with jump amplitude (amplitude-latency relation). When the eye started eccentrically, the latency was decreased (orbital position-latency relation), with the largest jump amplitudes most affected. These changes can be related to active eye-head coordination. Thus, with a leftward maximal orbital eccentricity, compensatory eye rotation would be impossible with a rightward head movement; however, incorporating the orbital position-latency relation, the forward ocular saccade is expedited by 90 ms. Conversely, with a primary starting position, the ocular component of an 80 degrees gaze saccade could be slowed 125 ms by incorporating the amplitude-latency relation, thus facilitating a head contribution to the gaze shift. The orbital position and amplitude-latency relations were prominent in those subjects with habitually large head contributions to the gaze shift and minimal in individuals with typically small head contributions.

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Year:  1996        PMID: 8817276     DOI: 10.1007/bf00229630

Source DB:  PubMed          Journal:  Exp Brain Res        ISSN: 0014-4819            Impact factor:   1.972


  17 in total

1.  Head movement propensity.

Authors:  J H Fuller
Journal:  Exp Brain Res       Date:  1992       Impact factor: 1.972

2.  Vestibuloocular reflex inhibition and gaze saccade control characteristics during eye-head orientation in humans.

Authors:  D Pelisson; C Prablanc; C Urquizar
Journal:  J Neurophysiol       Date:  1988-03       Impact factor: 2.714

3.  Eye and head coupled and dissociated movements during orientation to a double step visual target displacement.

Authors:  S Ron; A Berthoz
Journal:  Exp Brain Res       Date:  1991       Impact factor: 1.972

4.  Different programming modes of human saccadic eye movements as a function of stimulus eccentricity: indications of a functional subdivision of the visual field.

Authors:  D Frost; E Pöppel
Journal:  Biol Cybern       Date:  1976-06-18       Impact factor: 2.086

5.  Effects of eye position on saccades evoked electrically from superior colliculus of alert cats.

Authors:  J T McIlwain
Journal:  J Neurophysiol       Date:  1986-01       Impact factor: 2.714

6.  The contribution of coordinated eye and head movements in hand pointing accuracy.

Authors:  B Biguer; C Prablanc; M Jeannerod
Journal:  Exp Brain Res       Date:  1984       Impact factor: 1.972

7.  Vestibular-oculomotor interaction in cat eye-head movements.

Authors:  J H Fuller; H Maldonado; J Schlag
Journal:  Brain Res       Date:  1983-07-25       Impact factor: 3.252

8.  Saccadic responses evoked by presentation of visual and auditory targets.

Authors:  D Zambarbieri; R Schmid; G Magenes; C Prablanc
Journal:  Exp Brain Res       Date:  1982       Impact factor: 1.972

9.  The vestibulo-ocular reflex during human saccadic eye movements.

Authors:  V P Laurutis; D A Robinson
Journal:  J Physiol       Date:  1986-04       Impact factor: 5.182

10.  Presaccadic 'spike' potential: investigation of topography and source.

Authors:  G W Thickbroom; F L Mastaglia
Journal:  Brain Res       Date:  1985-07-29       Impact factor: 3.252

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  27 in total

1.  Experimental control of eye and head positions prior to head-unrestrained gaze shifts in monkey.

Authors:  N J Gandhi; D L Sparks
Journal:  Vision Res       Date:  2001       Impact factor: 1.886

2.  Effects of direction on saccadic performance in relation to lateral preferences.

Authors:  T S Constantinidis; N Smyrnis; I Evdokimidis; N C Stefanis; D Avramopoulos; I Giouzelis; C N Stefanis
Journal:  Exp Brain Res       Date:  2003-04-25       Impact factor: 1.972

3.  The control of vertical saccades in aged subjects.

Authors:  Qing Yang; Zoï Kapoula
Journal:  Exp Brain Res       Date:  2005-11-24       Impact factor: 1.972

4.  The effect of directional compatibility on the response latencies of ocular and manual movements.

Authors:  E Niechwiej-Szwedo; W E McIlroy; R Green; M C Verrier
Journal:  Exp Brain Res       Date:  2004-12-15       Impact factor: 1.972

5.  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

6.  Dissociation of eye and head components of gaze shifts by stimulation of the omnipause neuron region.

Authors:  Neeraj J Gandhi; David L Sparks
Journal:  J Neurophysiol       Date:  2007-05-09       Impact factor: 2.714

7.  Gaze displacement and inter-segmental coordination during large whole body voluntary rotations.

Authors:  Dimitri Anastasopoulos; Nausica Ziavra; Mark Hollands; Adolfo Bronstein
Journal:  Exp Brain Res       Date:  2008-11-12       Impact factor: 1.972

8.  Guidance of visual direction by topographical vibrotactile cues on the torso.

Authors:  Francois Asseman; Adolfo M Bronstein; Michael A Gresty
Journal:  Exp Brain Res       Date:  2007-12-11       Impact factor: 1.972

9.  Eye-head coordination in moderately affected Huntington's Disease patients: do head movements facilitate gaze shifts?

Authors:  W Becker; R Jürgens; J Kassubek; D Ecker; B Kramer; B Landwehrmeyer
Journal:  Exp Brain Res       Date:  2008-09-20       Impact factor: 1.972

10.  High-field FMRI reveals brain activation patterns underlying saccade execution in the human superior colliculus.

Authors:  Ruth M Krebs; Marty G Woldorff; Claus Tempelmann; Nils Bodammer; Toemme Noesselt; Carsten N Boehler; Henning Scheich; Jens-Max Hopf; Emrah Duzel; Hans-Jochen Heinze; Mircea A Schoenfeld
Journal:  PLoS One       Date:  2010-01-13       Impact factor: 3.240

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