Literature DB >> 3556487

Head movements during optokinetic stimulation in the alert rabbit.

J H Fuller.   

Abstract

Pigmented rabbits with their heads free to move about the vertical axis were seated inside a rotating optokinetic drum in order to evoke the optocollic reflex (OCR). At drum velocities below 5 degrees/s, head movements were inconsequential, and eye velocity generally matched drum velocity. At velocities between 5-15 degrees/s head movements were irregular and slight; head velocity was less than 20% of drum velocity, and gaze was undercompensatory by 1-3 degrees/s (retinal image motion of 1-3 degrees/s). At drum velocities above 15 degrees/s, and especially above 30 degrees/s, head movements were substantial (more than 20% of the drum velocity), but gaze was undercompensatory by 60-70% of the stimulus velocity. In the same rabbits in the same test periods and conditions, the vestibulo-collic reflex (VCR) was evoked with vision with minimal gaze undercompensation relative to a stationary surround; however, when deprived of vision the VCR gain dropped. The present results support the notion that with vision, the OCR does not contribute significantly to the improvement of the VCR response, since massive undercompensation of the gaze relative to the rotating drum was required in OCR testing to evoke head movements similar to those seen in VCR tests. Due to many differences in operating characteristics of the vestibular and optokinetic systems, and due to the nature of OCR testing, there were several unexpected results: in some cases head movements did not result in summation of vestibular and optokinetic reflexes, and with sinusoidal drum rotations of about 2 degrees/s2 peak acceleration there was overcompensation (gaze moves faster than the drum) for intervals up to 20 s. Thus, optokinetically generated active head movements could produce behavior strongly contrasting with passively induced head movements in visual-vestibular tests. It is tentatively concluded that in mammals there is a vestigial and specific optokinetic control of gaze and that the optokinetic control of the head is weak (relative to the eyes). However, other non-reflex mechanisms controlling head movements-such as stimulus entrainment and temporal asymmetries in the vestibular and optokinetic reflexes-must also be considered to explain all facets of the data.

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Year:  1987        PMID: 3556487     DOI: 10.1007/BF00235982

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


  25 in total

1.  Neural design of the cerebellar motor control system.

Authors:  M Ito
Journal:  Brain Res       Date:  1972-05-12       Impact factor: 3.252

2.  Optokinetic eye movements in the rabbit: input-output relations.

Authors:  H Collewijn
Journal:  Vision Res       Date:  1969-01       Impact factor: 1.886

3.  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

4.  The latency of pathways containing the site of motor learning in the monkey vestibulo-ocular reflex.

Authors:  S G Lisberger
Journal:  Science       Date:  1984-07-06       Impact factor: 47.728

5.  Horizontal eye position-related activity in neck muscles of the alert cat.

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

6.  Latency and gain of the rabbit's optokinetic reactions to small movements.

Authors:  H Collewijn
Journal:  Brain Res       Date:  1972-01-14       Impact factor: 3.252

7.  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

8.  Effects of pontine reticular formation lesions on optokinetic head nystagmus in rats.

Authors:  D W Sirkin; Y Zedek; P Teitelbaum
Journal:  Exp Brain Res       Date:  1985       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.  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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  5 in total

1.  Comparison of optomotor and optokinetic reflexes in mice.

Authors:  Friedrich Kretschmer; Momina Tariq; Walid Chatila; Beverly Wu; Tudor Constantin Badea
Journal:  J Neurophysiol       Date:  2017-04-19       Impact factor: 2.714

2.  Stabilizing gaze reflexes in the pigeon (Columba livia). II. Vestibulo-ocular (VOR) and vestibulo-collic (closed-loop VCR) reflexes.

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

3.  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

4.  The role of compensatory eye and head movements in the rat for image stabilization and gaze orientation.

Authors:  R K Meier; N Dieringer
Journal:  Exp Brain Res       Date:  1993       Impact factor: 1.972

5.  Visual function in guinea pigs: behavior and electrophysiology.

Authors:  Ashutosh Jnawali; Sudan Puri; Laura J Frishman; Lisa A Ostrin
Journal:  Clin Exp Optom       Date:  2021-02-27       Impact factor: 2.742

  5 in total

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