Literature DB >> 857007

Eye- and head movements in freely moving rabbits.

H Collewijn.   

Abstract

1. Eye- and head movements were recorded in unrestrained, spontaneously behaving rabbits with a new technique, based upon phase detection of signals induced in implanted coils by a rotating magnetic field. 2. Movements of the eye in space were exclusively saccadic. In the intersaccadic intervals the eyes were stabilized in space, even during vigorous head movements. Most of this stability was maintained in darkness, except for the occurrence of slow drift. 3. Many saccades were initiated while the head was stationary. They were accompanied by a similar, but slower head rotation with approximately the same amplitude. The displacement of the eye in space was a pure step without appreciable under- or over-shoot. The deviation of the eye in the head was mostly transient. 4. Other saccades were started while the head was moving and were possibly fast phases of a vestibulo-ocular reflex. The time course of the eye movement in space was identical for all saccades, whether the head was moving prior to the saccade or not. Eye movements without any head movement were not observed. 5. Saccades were mostly large (average 20-6 +/- 12-4 degrees S.D.) and never smaller than 1 degree. The relations of maximal velocity and duration to amplitude were similar to those reported for man. 6. Visual pursuit of moving objects, when elicited, was only saccadic and never smooth. 7. It is concluded that the co-ordination and dynamics of the rabbit's head- and eye movements are similar to those of primates. In the absence of foveal specilization, the eye movements are restricted to a rather global redirection of the visual field, possibly in particular of the binocular area.

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Mesh:

Year:  1977        PMID: 857007      PMCID: PMC1283576          DOI: 10.1113/jphysiol.1977.sp011778

Source DB:  PubMed          Journal:  J Physiol        ISSN: 0022-3751            Impact factor:   5.182


  28 in total

1.  Closely spaced saccades.

Authors:  A T Bahill; K A Bahill; M R Clark; L Stark
Journal:  Invest Ophthalmol       Date:  1975-04

2.  Most naturally occurring human saccades have magnitudes of 15 degrees or less.

Authors:  A T Bahill; D Adler; L Stark
Journal:  Invest Ophthalmol       Date:  1975-06

3.  Quantitative measurement of saccade amplitude, duration, and velocity.

Authors:  R W Baloh; A W Sills; W E Kumley; V Honrubia
Journal:  Neurology       Date:  1975-11       Impact factor: 9.910

4.  Fixation by the alert but solitary cat.

Authors:  B J Winterson; D A Robinson
Journal:  Vision Res       Date:  1975-12       Impact factor: 1.886

5.  Voluntary, non-visual control of the human vestibulo-ocular reflex.

Authors:  C C Barr; L W Schultheis; D A Robinson
Journal:  Acta Otolaryngol       Date:  1976 May-Jun       Impact factor: 1.494

6.  Miniature eye movements of fixation in rhesus monkey.

Authors:  A A Skavenski; D A Robinson; R M Steinman; G T Timberlake
Journal:  Vision Res       Date:  1975-11       Impact factor: 1.886

7.  Mechanisms underlying recovery of eye-head coordination following bilateral labyrinthectomy in monkeys.

Authors:  J Dichgans; E Bizzi; P Morasso; V Tagliasco
Journal:  Exp Brain Res       Date:  1973-12-20       Impact factor: 1.972

8.  A reexamination of "neck reflex" eye movements in the rabbit.

Authors:  M A Gresty
Journal:  Acta Otolaryngol       Date:  1976 May-Jun       Impact factor: 1.494

9.  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

10.  Eye, head and body movements of the guinea pig in response to optokinetic stimulation and sinusoidal oscillation in yaw.

Authors:  M A Gresty
Journal:  Pflugers Arch       Date:  1975       Impact factor: 3.657

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  74 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.  Adaptation of the vestibulo-ocular reflex for forward-eyed foveate vision.

Authors:  Americo A Migliaccio; Lloyd B Minor; Charles C Della Santina
Journal:  J Physiol       Date:  2010-08-19       Impact factor: 5.182

3.  Head-eye interactions during vertical gaze shifts made by rhesus monkeys.

Authors:  Edward G Freedman
Journal:  Exp Brain Res       Date:  2005-08-13       Impact factor: 1.972

4.  Discharge of monkey nucleus reticularis tegmenti pontis neurons changes during saccade adaptation.

Authors:  N Takeichi; C R S Kaneko; A F Fuchs
Journal:  J Neurophysiol       Date:  2005-05-25       Impact factor: 2.714

5.  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

6.  Eye position modulates the electromyographic responses of neck muscles to electrical stimulation of the superior colliculus in the alert cat.

Authors:  K Hadjidimitrakis; A K Moschovakis; Y Dalezios; A Grantyn
Journal:  Exp Brain Res       Date:  2006-11-08       Impact factor: 1.972

7.  The impact of a corticotectal impulse on the awake superior colliculus.

Authors:  Yulia Bereshpolova; Carl R Stoelzel; Alexander G Gusev; Tatiana Bezdudnaya; Harvey A Swadlow
Journal:  J Neurosci       Date:  2006-02-22       Impact factor: 6.167

Review 8.  The significance of microsaccades for vision and oculomotor control.

Authors:  Han Collewijn; Eileen Kowler
Journal:  J Vis       Date:  2008-12-18       Impact factor: 2.240

9.  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

10.  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

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