Literature DB >> 2026189

Pursuit afternystagmus asymmetry in humans.

A Chaudhuri1.   

Abstract

It is known that prolonged unidirectional motion of a large field induces a reflexive drift of the eyes in the same direction when the stimulus is turned off. The phenomenon, which is called optokinetic afternystagmus, is known to be stronger after upward than downward stimulus motion. It is now reported that a similar anisotropy exists in the afternystagmus associated with the smooth pursuit system (PAN). The speed of the PAN reflexive drift was found to be greater following upward tracking at all times tested during a 15 s interval when compared to the values following downward tracking. A psychophysical measure of illusory motion, presumed to be generated by suppression of PAN in order to maintain fixation upon a stationary target, also showed a significantly greater amplitude and duration for the upward direction. If the directional asymmetry is a property of a velocity integrator that is believed to generate the afternystagmus, then the results are compatible with the existence of a common integrator for both optokinetic and pursuit systems.

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Year:  1991        PMID: 2026189     DOI: 10.1007/bf00229823

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


  48 in total

Review 1.  Contribution of the nucleus of the optic tract to optokinetic nystagmus and optokinetic afternystagmus in the monkey: clinical implications.

Authors:  B Cohen; D Schiff; J Buettner
Journal:  Res Publ Assoc Res Nerv Ment Dis       Date:  1990

2.  The role of the primate lateral terminal nucleus in visuomotor behavior.

Authors:  M J Mustari; A F Fuchs; T P Langer; C Kaneko; J Wallman
Journal:  Prog Brain Res       Date:  1988       Impact factor: 2.453

3.  Asymmetry of vertical optokinetic after-nystagmus in squirrel monkeys.

Authors:  T Himi; M Igarashi; W B Kulecz; A Kataura
Journal:  Acta Otolaryngol       Date:  1988 Mar-Apr       Impact factor: 1.494

4.  Some characteristics of optokinetic eye-movement patterns: a comparative study.

Authors:  W E Collins; D J Schroeder; N Rice; R A Mertens; G Kranz
Journal:  Aerosp Med       Date:  1970-11

5.  An autoradiographic study of the pathways from the pontine reticular formation involved in horizontal eye movements.

Authors:  J A Büttner-Ennever; V Henn
Journal:  Brain Res       Date:  1976-05-21       Impact factor: 3.252

6.  Columnar organization of directionally selective cells in visual area MT of the macaque.

Authors:  T D Albright; R Desimone; C G Gross
Journal:  J Neurophysiol       Date:  1984-01       Impact factor: 2.714

7.  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

8.  Effects of ablation of flocculus and paraflocculus of eye movements in primate.

Authors:  D S Zee; A Yamazaki; P H Butler; G Gücer
Journal:  J Neurophysiol       Date:  1981-10       Impact factor: 2.714

9.  Afferents to the flocculus of the cerebellum in the rhesus macaque as revealed by retrograde transport of horseradish peroxidase.

Authors:  T Langer; A F Fuchs; C A Scudder; M C Chubb
Journal:  J Comp Neurol       Date:  1985-05-01       Impact factor: 3.215

10.  Role of the flocculus and paraflocculus in optokinetic nystagmus and visual-vestibular interactions: effects of lesions.

Authors:  W Waespe; B Cohen; T Raphan
Journal:  Exp Brain Res       Date:  1983       Impact factor: 1.972

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  2 in total

1.  Extra-retinal adaptation of cortical motion-processing areas during pursuit eye movements.

Authors:  Tom C A Freeman; Jane H Sumnall
Journal:  Proc Biol Sci       Date:  2005-10-22       Impact factor: 5.349

2.  Anticipatory smooth-pursuit eye movements in man and monkey.

Authors:  Sylvana Freyberg; Uwe J Ilg
Journal:  Exp Brain Res       Date:  2007-12-05       Impact factor: 1.972

  2 in total

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