Literature DB >> 6332740

Ocular stability in the horizontal, frontal and sagittal planes in the rabbit.

J Van der Steen, H Collewijn.   

Abstract

Eye and head movements in the horizontal, frontal and sagittal planes were recorded in the rabbit with a newly developed technique using dual scleral search coils in a rotating magnetic field. The compensatory eye movements elicited by passive sinusoidal oscillation deteriorated for frequencies below 0.1 Hz in the horizontal, but not in the frontal and sagittal planes. In the light gain was relatively independent of frequency in all planes and amounted to 0.82-0.69, 0.92-0.83 and 0.65-0.59 in the horizontal, frontal and sagittal plane, respectively. In freely moving animals, similar input-output relations were found. The stability of the retinal image thus proved to be inversely proportional to the amount of head movements associated with behavioural activity. Maximal retinal image velocities varied between 2-4 degree/s for a rabbit sitting quietly and 30-40 degrees/s during locomotor activity. Gaze displacements showed different characteristics in the various planes, possibly in relation with the structure of the retinal visual streak. Horizontal gaze changes were mainly effected by saccades. Gaze changes in the frontal plane were relatively rare and effected by non-saccadic, combined head and eye movements with temporary suppression of compensatory eye movements. Eye rotations in the sagittal plane, possibly functioning to adjust the direction of binocular vision vertically, were abundant and effected by large head movements in combination with a low gain of compensatory eye movements in this plane.

Entities:  

Mesh:

Year:  1984        PMID: 6332740     DOI: 10.1007/bf00236282

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


  22 in total

1.  The optokinetic reactions of the rabbit: relation to the visual streak.

Authors:  M F Dubois; H Collewijn
Journal:  Vision Res       Date:  1979       Impact factor: 1.886

2.  The retinal fixation area in the rabbit.

Authors:  M W van Hof; G C Lagers-van Haselen
Journal:  Exp Neurol       Date:  1973-10       Impact factor: 5.330

3.  Vertical and torsional optokinetic eye movements in the rabbit.

Authors:  H Collewijn; H Noorduin
Journal:  Pflugers Arch       Date:  1972       Impact factor: 3.657

4.  Adaptation of optokinetic and vestibulo-ocular reflexes to modified visual input in the rabbit.

Authors:  H Collewijn; A F Grootendorst
Journal:  Prog Brain Res       Date:  1979       Impact factor: 2.453

5.  A comparison of the horizontal and vertical optokinetic reflexes of the rabbit.

Authors:  R G Erickson; N H Barmack
Journal:  Exp Brain Res       Date:  1980       Impact factor: 1.972

6.  Eye movements due to linear accelerations in the rabbit.

Authors:  E A Baarsma; H Collewijn
Journal:  J Physiol       Date:  1975-02       Impact factor: 5.182

7.  Interaction between the horizontal vestibulo-ocular reflex and optokinetic response in rabbits.

Authors:  C Batini; M Ito; R T Kado; P J Jastreboff; Y Miyashita
Journal:  Exp Brain Res       Date:  1979-09       Impact factor: 1.972

8.  Adaptive modification of the rabbit's horizontal vestibulo-ocular reflex during sustained vestibular and optokinetic stimulation.

Authors:  M Ito; P J Jastreboff; Y Miyashita
Journal:  Exp Brain Res       Date:  1979-09       Impact factor: 1.972

9.  Post-rotary nystagmus and optokinetic after-nystagmus in the rabbit linear rather than exponential decay.

Authors:  H Collewijn; B J Winterson; J van der Steen
Journal:  Exp Brain Res       Date:  1980       Impact factor: 1.972

10.  Vestibulo-ocular and optokinetic reactions to rotation and their interaction in the rabbit.

Authors:  E Baarsma; H Collewijn
Journal:  J Physiol       Date:  1974-05       Impact factor: 5.182

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  15 in total

1.  How much the eye tells the brain.

Authors:  Kristin Koch; Judith McLean; Ronen Segev; Michael A Freed; Michael J Berry; Vijay Balasubramanian; Peter Sterling
Journal:  Curr Biol       Date:  2006-07-25       Impact factor: 10.834

2.  Head position modulates optokinetic nystagmus.

Authors:  V E Pettorossi; A Ferraresi; F M Botti; R Panichi; N H Barmack
Journal:  Exp Brain Res       Date:  2011-07-07       Impact factor: 1.972

3.  Dynamics and directionality of the vestibulo-collic reflex (VCR) in mice.

Authors:  James F Baker
Journal:  Exp Brain Res       Date:  2005-10-29       Impact factor: 1.972

4.  European vestibular experiments on the Spacelab-1 mission: 5. Contribution of the otoliths to the vertical vestibulo-ocular reflex.

Authors:  A Berthoz; T Brandt; J Dichgans; T Probst; W Bruzek; T Viéville
Journal:  Exp Brain Res       Date:  1986       Impact factor: 1.972

5.  Global Motion Processing by Populations of Direction-Selective Retinal Ganglion Cells.

Authors:  Jon Cafaro; Joel Zylberberg; Greg D Field
Journal:  J Neurosci       Date:  2020-06-19       Impact factor: 6.167

6.  Binocular eye movement control and motion perception: what is being tracked?

Authors:  Johannes van der Steen; Joyce Dits
Journal:  Invest Ophthalmol Vis Sci       Date:  2012-10-19       Impact factor: 4.799

7.  Human ocular counterroll: assessment of static and dynamic properties from electromagnetic scleral coil recordings.

Authors:  H Collewijn; J Van der Steen; L Ferman; T C Jansen
Journal:  Exp Brain Res       Date:  1985       Impact factor: 1.972

8.  Peaks and troughs of three-dimensional vestibulo-ocular reflex in humans.

Authors:  Janine Goumans; Mark M J Houben; Joyce Dits; Johannes van der Steen
Journal:  J Assoc Res Otolaryngol       Date:  2010-02-23

9.  Head movements during optokinetic stimulation in the alert rabbit.

Authors:  J H Fuller
Journal:  Exp Brain Res       Date:  1987       Impact factor: 1.972

10.  Optokinetic and vestibular stimulation determines the spatial orientation of negative optokinetic afternystagmus in the rabbit.

Authors:  V E Pettorossi; P Errico; A Ferraresi; N H Barmack
Journal:  J Neurosci       Date:  1999-02-15       Impact factor: 6.167

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