Literature DB >> 2394230

Optokinetic nystagmus and afternystagmus in human beings: relationship to nonlinear processing of information about retinal slip.

W A Fletcher1, T C Hain, D S Zee.   

Abstract

In four normal human subjects we measured eye movements during full-field optokinetic stimulation (10-220 deg/s) and determined the relationship among retinal-slip velocity (drum velocity minus slow-phase eye velocity), the slow-phase velocity of optokinetic nystagmus (OKN) and the initial value of the slow-phase velocity of optokinetic afternystagmus (OKAN) measured in darkness. OKN and OKAN were maximum (63-84 and 11-19 deg/s, respectively) when retinal slip ranged from 30-100 deg/s. For higher values of retinal slip, OKN and OKAN fell (in 3 subjects) or reached a plateau (in the fourth). The amplitude of OKAN in human beings was much less than that reported in monkeys. The shape, however, of the curve relating retinal slip to the amplitude of OKAN was similar to that of monkeys. Furthermore, in both cases the curve resembles that obtained by plotting the results of experimental recordings of neural discharge in the nucleus of the optic tract as a function of retinal slip. These results imply that the processing of visual information for generation of OKAN is similar in monkeys and human beings but that the gain of the system is much less in human beings. We also found that fixation of a small target during optokinetic stimulation nearly completely prevented the development of OKAN while fixation of a small target for short periods after optokinetic stimulation did not alter the pattern of decay of OKAN. Thus, fixation may actively prevent the coupling of visual information into the velocity-storage mechanism.

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Year:  1990        PMID: 2394230     DOI: 10.1007/bf00230099

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


  21 in total

1.  Effects of occipital lobectomy upon eye movements in primate.

Authors:  D S Zee; R J Tusa; S J Herdman; P H Butler; G Gücer
Journal:  J Neurophysiol       Date:  1987-10       Impact factor: 2.714

2.  Physiological and anatomical identification of the nucleus of the optic tract and dorsal terminal nucleus of the accessory optic tract in monkeys.

Authors:  K P Hoffmann; C Distler; R G Erickson; W Mader
Journal:  Exp Brain Res       Date:  1988       Impact factor: 1.972

3.  Motion habituation: inverted self-motion perception and optokinetic after-nystagmus.

Authors:  T Brandt; J Dichgans; W Büchle
Journal:  Exp Brain Res       Date:  1974       Impact factor: 1.972

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

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

5.  Modulation of human velocity storage sampled during intermittently-illuminated optokinetic stimulation.

Authors:  B N Segal; S Liben
Journal:  Exp Brain Res       Date:  1985       Impact factor: 1.972

6.  Optokinetic response in monkey: underlying mechanisms and their sensitivity to long-term adaptive changes in vestibuloocular reflex.

Authors:  S G Lisberger; F A Miles; L M Optican; B B Eighmy
Journal:  J Neurophysiol       Date:  1981-05       Impact factor: 2.714

7.  Nystagmus induced by stimulation of the nucleus of the optic tract in the monkey.

Authors:  D Schiff; B Cohen; T Raphan
Journal:  Exp Brain Res       Date:  1988       Impact factor: 1.972

8.  A quantitative analysis of the direction-specific response of Neurons in the cat's nucleus of the optic tract.

Authors:  K P Hoffmann; A Schoppmann
Journal:  Exp Brain Res       Date:  1981       Impact factor: 1.972

9.  Influence of vestibulo-ocular reflex gain on human optokinetic responses.

Authors:  N L Zasorin; R W Baloh; R D Yee; V Honrubia
Journal:  Exp Brain Res       Date:  1983       Impact factor: 1.972

10.  Role of the nucleus of the optic tract of monkeys in optokinetic nystagmus and optokinetic after-nystagmus.

Authors:  I Kato; K Harada; T Hasegawa; T Ikarashi
Journal:  Brain Res       Date:  1988-11-22       Impact factor: 3.252

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  13 in total

1.  Prolonged reduction of motion sickness sensitivity by visual-vestibular interaction.

Authors:  Mingjia Dai; Ted Raphan; Bernard Cohen
Journal:  Exp Brain Res       Date:  2011-02-02       Impact factor: 1.972

2.  Velocity storage activity is affected after sustained centrifugation: a relationship with spatial disorientation.

Authors:  Suzanne A E Nooij; Jelte E Bos; Eric L Groen
Journal:  Exp Brain Res       Date:  2008-06-20       Impact factor: 1.972

3.  "Dumping" of rebound nystagmus and optokinetic afternystagmus in humans.

Authors:  S T Chung; H E Bedell
Journal:  Exp Brain Res       Date:  1995       Impact factor: 1.972

4.  Afternystagmus in darkness after suppression of optokinetic nystagmus: an interaction of motion aftereffect and retinal afterimages.

Authors:  Chien-Cheng Chen; Melody Ying-Yu Huang; Konrad P Weber; Dominik Straumann; Christopher J Bockisch
Journal:  Exp Brain Res       Date:  2014-05-13       Impact factor: 1.972

5.  The effect of aging on visual-vestibuloocular responses.

Authors:  R W Baloh; K M Jacobson; T M Socotch
Journal:  Exp Brain Res       Date:  1993       Impact factor: 1.972

6.  Short-term vestibulo-ocular reflex adaptation in humans. II. Error signals.

Authors:  M Shelhamer; C Tiliket; D Roberts; P D Kramer; D S Zee
Journal:  Exp Brain Res       Date:  1994       Impact factor: 1.972

7.  Optokinetic-vestibular interaction in patients with increased gain of the vestibulo-ocular reflex.

Authors:  R W Baloh; J L Demer
Journal:  Exp Brain Res       Date:  1993       Impact factor: 1.972

8.  Correlation between vestibulo-ocular reflex and optokinetic afternystagmus in normal subjects and in patients with vestibular system disorders.

Authors:  M Dellepiane; M C Medicina; L Barettini; A C Mura
Journal:  Acta Otorhinolaryngol Ital       Date:  2006-02       Impact factor: 2.124

9.  Orientation of human optokinetic nystagmus to gravity: a model-based approach.

Authors:  M Gizzi; T Raphan; S Rudolph; B Cohen
Journal:  Exp Brain Res       Date:  1994       Impact factor: 1.972

10.  Adaptive Acceleration of Visually Evoked Smooth Eye Movements in Mice.

Authors:  Takashi Kodama; Sascha du Lac
Journal:  J Neurosci       Date:  2016-06-22       Impact factor: 6.167

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