Literature DB >> 1884758

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

S Ron1, A Berthoz.   

Abstract

Tight coupling between eye and head movements has been observed in response to a single visual target offset. On this basis, when the visual stimulus consists of two successive steps in the same (horizontal) direction, either increasing in eccentricity (staircase) or decreasing in eccentricity (pulse-step) gaze should be due to concomitant eye and head angular displacement. That is, the eyes and head should aim at each target displacement so that their combined movement matches target offset. We have tested this hypothesis in five healthy subjects. The measured variables were head and gaze offset, the interval between two consecutive saccades from onset to onset (I) and the response delay between onset of the second step and onset of the first gaze saccade (D). With both staircase and pulse-step stimuli, the eye saccade preceded the head movement, and the gaze response either had the stimulus profile pattern or consisted of one gaze saccade to the final target offset. In response to staircase stimuli, I decreased concomitantly with an increase in D; with pulse-step stimuli, as D increased, I decreased slightly in three subjects and decreased markedly in two subjects. Dissociation between the eye and head movements could clearly be demonstrated with pulse-step stimuli: the first gaze saccade to the target pulse displacement was accompanied by a head movement to the target step offset. We also observed cases in which the gaze saccade to the target step displacement was made simultaneously with the head movement to the target pulse offset. Our study extends previous observations in head fixed condition and illustrates that in the majority of cases, when the head is free and a visual pulse step stimulus is presented, both the saccadic and head systems have the ability to modify or cancel the initial neural command to move to the first target displacement. When this modification takes place in only one system, eye and head movements are dissociated.

Mesh:

Year:  1991        PMID: 1884758     DOI: 10.1007/bf00230001

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


  27 in total

1.  Effect of mean reaction time on saccadic responses to two-step stimuli with horizontal and vertical components.

Authors:  S G Lisberger; A F Fuchs; W M King; L C Evinger
Journal:  Vision Res       Date:  1975 Aug-Sep       Impact factor: 1.886

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

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Authors:  R D Tomlinson; P S Bahra
Journal:  J Neurophysiol       Date:  1986-12       Impact factor: 2.714

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Authors:  M A Gresty
Journal:  Vision Res       Date:  1974-06       Impact factor: 1.886

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Authors:  M K Komoda; L Festinger; L J Phillips; R H Duckman; R A Young
Journal:  Vision Res       Date:  1973-06       Impact factor: 1.886

6.  Gaze changing behaviour in head restrained monkey.

Authors:  F Lestienne; P P Vidal; A Berthoz
Journal:  Exp Brain Res       Date:  1984       Impact factor: 1.972

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Authors:  P P Vidal; A Roucoux; A Berthoz
Journal:  Exp Brain Res       Date:  1982       Impact factor: 1.972

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Authors:  W H Zangemeister; S Lehman; L Stark
Journal:  Biol Cybern       Date:  1981       Impact factor: 2.086

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Authors:  E Bizzi; R E Kalil; P Morasso
Journal:  Brain Res       Date:  1972-05-12       Impact factor: 3.252

10.  Eye and head movements during vestibular stimulation in the alert rabbit.

Authors:  J H Fuller
Journal:  Brain Res       Date:  1981-02-02       Impact factor: 3.252

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  11 in total

1.  Independent control of head and gaze movements during head-free pursuit in humans.

Authors:  C J Collins; G R Barnes
Journal:  J Physiol       Date:  1999-02-15       Impact factor: 5.182

2.  On the short-term adaptation of eye saccades and its transfer to head movements.

Authors:  J Kröller; D Pélisson; C Prablanc
Journal:  Exp Brain Res       Date:  1996-10       Impact factor: 1.972

Review 3.  The functions of the proprioceptors of the eye muscles.

Authors:  I M Donaldson
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2000-12-29       Impact factor: 6.237

4.  Eye-head-hand coordination during visually guided reaches in head-unrestrained macaques.

Authors:  Harbandhan Kaur Arora; Vishal Bharmauria; Xiaogang Yan; Saihong Sun; Hongying Wang; John Douglas Crawford
Journal:  J Neurophysiol       Date:  2019-09-18       Impact factor: 2.714

5.  Combined eye-head gaze shifts to visual and auditory targets in humans.

Authors:  J E Goldring; M C Dorris; B D Corneil; P A Ballantyne; D P Munoz
Journal:  Exp Brain Res       Date:  1996-09       Impact factor: 1.972

6.  Slow correcting eye movements of head-fixed, trained cats toward stationary targets.

Authors:  M Missal; M Crommelinck; A Roucoux; M F Decostre
Journal:  Exp Brain Res       Date:  1993       Impact factor: 1.972

7.  Facial input to neck motoneurons: trigemino-cervical reflexes in the conscious and anaesthetised cat.

Authors:  V C Abrahams; A A Kori; G E Loeb; F J Richmond; P K Rose; S A Keirstead
Journal:  Exp Brain Res       Date:  1993       Impact factor: 1.972

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

Authors:  J H Fuller
Journal:  Exp Brain Res       Date:  1996-06       Impact factor: 1.972

9.  Human gaze shifts in which head and eyes are not initially aligned.

Authors:  M Volle; D Guitton
Journal:  Exp Brain Res       Date:  1993       Impact factor: 1.972

10.  The mesencephalic reticular formation as a conduit for primate collicular gaze control: tectal inputs to neurons targeting the spinal cord and medulla.

Authors:  Eddie Perkins; Susan Warren; Paul J May
Journal:  Anat Rec (Hoboken)       Date:  2009-08       Impact factor: 2.064

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