Literature DB >> 7470870

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

J H Fuller.   

Abstract

Rabbits passively oscillated in the horizontal plane with a free hand tended to stabilize their head in space (re: earth-fixed surroundings) by moving the head on the trunk (neck angular deviation, NAD) opposite the passively imposed body rotation. The gain (NAD/body rotation) of head stabilization varied from 0.0 to 0.95 (nearly perfect stability) and was most commonly above 0.5. Horizontal eye movement (HEM) was inversely proportional to head-in-space stability, i.e. the gaze (sum of HEM, NAD, and body rotation) was stable in space (regardless of the gain of head stabilization). When the head was fixed to the rotating platform, attempted head movements (head torque) mimicked eye movements in both the slow and fast phases of vestibular nystagmus; tonic eye position was also accompanied by conjugate shifts in tonic head torque. Thus, while eye and head movements may at times be linked, that the slow eye and head movements vary inversely during vestibular stimulation with a free head indicates that the linkage is not rigid. Absence of a textured stationary visual field consistently produced a response termed 'visual inattentiveness,' which was characterized by, among other things, a reduction of head and gaze stability in space. This behavioral response could also be reproduced in a subject allowed vision during prolonged vestibular stimulation in the absence of other environmental stimuli. It is suggested that rabbits optimize gaze stability (re: stationary surroundings), with the head contributing variably, as long as the animal is attending to its surroundings.

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Year:  1981        PMID: 7470870     DOI: 10.1016/0006-8993(81)90346-2

Source DB:  PubMed          Journal:  Brain Res        ISSN: 0006-8993            Impact factor:   3.252


  20 in total

1.  The influence of future gaze orientation upon eye-head coupling during saccades.

Authors:  Brian S Oommen; Ryan M Smith; John S Stahl
Journal:  Exp Brain Res       Date:  2003-11-12       Impact factor: 1.972

2.  Head movement propensity.

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

3.  Eye-head coupling in humans. II. Phasic components.

Authors:  C André-Deshays; M Revel; A Berthoz
Journal:  Exp Brain Res       Date:  1991       Impact factor: 1.972

4.  Overlapping gaze shifts reveal timing of an eye-head gate.

Authors:  Brian S Oommen; John S Stahl
Journal:  Exp Brain Res       Date:  2005-07-21       Impact factor: 1.972

5.  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

6.  Layer 4 in primary visual cortex of the awake rabbit: contrasting properties of simple cells and putative feedforward inhibitory interneurons.

Authors:  Jun Zhuang; Carl R Stoelzel; Yulia Bereshpolova; Joseph M Huff; Xiaojuan Hei; Jose-Manuel Alonso; Harvey A Swadlow
Journal:  J Neurosci       Date:  2013-07-10       Impact factor: 6.167

7.  Hour-long adaptation in the awake early visual system.

Authors:  Carl R Stoelzel; Joseph M Huff; Yulia Bereshpolova; Jun Zhuang; Xiaojuan Hei; Jose-Manuel Alonso; Harvey A Swadlow
Journal:  J Neurophysiol       Date:  2015-06-24       Impact factor: 2.714

8.  Gravito-inertial ambiguity resolved through head stabilization.

Authors:  Ildar Farkhatdinov; Hannah Michalska; Alain Berthoz; Vincent Hayward
Journal:  Proc Math Phys Eng Sci       Date:  2019-03-27       Impact factor: 2.704

9.  Stabilizing gaze reflexes in the pigeon (Columba livia). I. Horizontal and vertical optokinetic eye (OKN) and head (OCR) reflexes.

Authors:  H Gioanni
Journal:  Exp Brain Res       Date:  1988       Impact factor: 1.972

10.  Eye and neck motor signals in periabducens reticular neurons of the alert cat.

Authors:  P P Vidal; J Corvisier; A Berthoz
Journal:  Exp Brain Res       Date:  1983       Impact factor: 1.972

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