Literature DB >> 3427473

Influence of long-term optokinetic stimulation on eye movements of the rabbit.

N H Barmack1, B J Nelson.   

Abstract

Two kinds of optokinetic afternystagmus (OKAN) have been studied in rabbits; positive and negative OKAN. Positive OKAN is the persistence of eye movements evoked by optokinetic stimulation following the termination of the stimulus, with the slow phase of the eye movements in the same direction as the inducing stimulus. Negative OKAN is evoked by long duration optokinetic stimulation, and has a slow phase of opposite direction to the inducing stimulus. The stimulus conditions which are optimal for inducing and maintaining negative OKAN were characterized. Rabbits were placed in an optokinetic drum for periods of 12-96 h (with appropriate intervening periods for food and water). Eye movements were recorded during and after the termination of optokinetic stimulation. The optimum optokinetic stimulus velocity for the induction of negative OKAN was 5 degrees/s. The minimum duration of stimulation for the induction of negative OKAN of maximum velocity was 48 h. Once induced, the slow phase of negative OKAN attained velocities of 50-100 degrees/s. Three conditions of restraint of the rabbits were studied after negative OKAN was induced during the intervening periods when eye movements were not being recorded. These conditions were: (1) unrestrained (full freedom of movement) without visual stimulation (in a dark enclosure); (2) restrained (horizontal head and body movement prevented) without visual stimulation; and (3) restrained with visual stimulation (in the stationary optokinetic drum). Conditions 1 and 2 caused negative OKAN to dissipate within 24 h. Condition 3 caused negative OKAN to be maintained for more than 70 h. The velocity imbalance of the horizontal vestibuloocular reflex (HVOR) was measured at different times following the induction of negative OKAN. It provided a more sensitive index of the central imbalance which caused negative OKAN, than did spontaneous nystagmus. One of the consequences of optokinetic stimulation measured over a 16 h period was a decrease in the gain of the optokinetic reflex. This reduction in gain could represent a central adaptation to maintained stimulation which in the absence of continued optokinetic stimulation is expressed as a nystagmus.

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Mesh:

Year:  1987        PMID: 3427473     DOI: 10.1016/0006-8993(87)91532-0

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


  10 in total

1.  Climbing fibers induce microRNA transcription in cerebellar Purkinje cells.

Authors:  N H Barmack; Z Qian; V Yakhnitsa
Journal:  Neuroscience       Date:  2010-09-25       Impact factor: 3.590

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.  Climbing fiber activity reduces 14-3-3-θ regulated GABA(A) receptor phosphorylation in cerebellar Purkinje cells.

Authors:  Z Qian; M Micorescu; V Yakhnitsa; N H Barmack
Journal:  Neuroscience       Date:  2011-11-17       Impact factor: 3.590

Review 4.  Long-term climbing fibre activity induces transcription of microRNAs in cerebellar Purkinje cells.

Authors:  Neal H Barmack; Zuyuan Qian; Vadim Yakhnitsa
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2014-09-26       Impact factor: 6.237

5.  Climbing fiber-evoked Purkinje cell discharge reduces expression of GABA(A) receptor-associated protein and decreases its interaction with GABA(A) receptors.

Authors:  Zuyuan Qian; Vadim Yakhnitsa; Neal H Barmack
Journal:  J Neurochem       Date:  2011-03-08       Impact factor: 5.372

6.  Activity-dependent expression of acyl-coenzyme a-binding protein in retinal muller glial cells evoked by optokinetic stimulation.

Authors:  Neal H Barmack; Timothy R Bilderback; Henry Liu; Zuyuan Qian; Vadim Yakhnitsa
Journal:  J Neurosci       Date:  2004-02-04       Impact factor: 6.167

7.  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

8.  Spontaneous Nystagmus in the Dark in an Infantile Nystagmus Patient May Represent Negative Optokinetic Afternystagmus.

Authors:  Ting-Feng Lin; Christina Gerth-Kahlert; James V M Hanson; Dominik Straumann; Melody Ying-Yu Huang
Journal:  Front Neurol       Date:  2018-03-14       Impact factor: 4.003

9.  Effect of the Stimulus Duration on the Adaptation of the Optokinetic Afternystagmus.

Authors:  Jan Gygli; Fausto Romano; Christopher J Bockisch; Nina Feddermann-Demont; Dominik Straumann; Giovanni Bertolini
Journal:  Front Neurol       Date:  2021-03-31       Impact factor: 4.003

10.  Negative optokinetic afternystagmus in larval zebrafish demonstrates set-point adaptation.

Authors:  Ting-Feng Lin; Mohammad Mohammadi; Ahmed M Fathalla; Duygu Pul; Dennis Lüthi; Fausto Romano; Dominik Straumann; Kathleen E Cullen; Maurice J Chacron; Melody Ying-Yu Huang
Journal:  Sci Rep       Date:  2019-12-13       Impact factor: 4.379

  10 in total

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