Literature DB >> 3794773

Short-latency ocular following responses of monkey. II. Dependence on a prior saccadic eye movement.

K Kawano, F A Miles.   

Abstract

The ocular following responses elicited by brief unexpected movements of the visual scene were studied in eight rhesus monkeys. Test patterns were random dots except in one experiment when sine-wave gratings were used. Test stimuli were velocity steps of 100-ms duration applied after spontaneous saccades. Two response measures were used: the initial peak in the eye velocity profile (ei), and the average final eye velocity over the period of 110-140 ms measured from stimulus onset (ef). Responses were best when the test ramps began soon after saccades and attenuated progressively as the postsaccadic delay interval was increased: postsaccadic enhancement of ocular following. The decline in ei was roughly exponential: average time constant, 60 ms; average asymptote, 22%. Later measures (ef) were generally less affected. We suggest that this transient enhancement aids the visual suppression of postsaccadic ocular drifts (glissades) and the tracking of moving images newly acquired with a saccade. The magnitude of the postsaccadic enhancement was dependent on the amount of retinal stimulation during the antecedent saccade; when this stimulation was compromised, as when a vertical saccade was made while viewing a grating pattern with vertically oriented stripes, subsequent enhancement of ocular following was much reduced. Further, saccade-like conditioning movements of the visual scene resulted in an enhancement of the ocular following, elicited by subsequent test ramps, that was similar in magnitude and time course to that in the wake of real saccades. We conclude that the postsaccadic enhancement of ocular following is largely due to the visual stimulation produced by the saccade sweeping the scene across the retina. Data obtained with the visual field partitioned into central and peripheral regions (center 20-60 degrees diam) and with gaze centered suggested that the short-latency ocular following system and the enhancement mechanism that modulates it both receive their major inputs from the central 40 degrees of the retina. Further, when this central region was partitioned, enhancement was obtained only when the conditioning and test stimuli were presented to the same region of retina. Visual enhancement showed only weak interocular transfer: the conditioning and test stimuli had to be seen by the same eye to produce appreciable enhancement. These data suggest that the enhancement involves local spatial interactions at an "early" point in the visual pathway before the inputs from the two eyes have converged. When the conditioning and test stimuli impinged on different regions of the retina, brief powerful suppression of ocular following was obtained.(ABSTRACT TRUNCATED AT 400 WORDS)

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Year:  1986        PMID: 3794773     DOI: 10.1152/jn.1986.56.5.1355

Source DB:  PubMed          Journal:  J Neurophysiol        ISSN: 0022-3077            Impact factor:   2.714


  31 in total

1.  Reversed short-latency ocular following.

Authors:  G S Masson; D-S Yang; F A Miles
Journal:  Vision Res       Date:  2002-08       Impact factor: 1.886

2.  Parallel motion processing for the initiation of short-latency ocular following in humans.

Authors:  Guillaume S Masson; Eric Castet
Journal:  J Neurosci       Date:  2002-06-15       Impact factor: 6.167

3.  Short-latency ocular following in humans is dependent on absolute (rather than relative) binocular disparity.

Authors:  D-S Yang; F A Miles
Journal:  Vision Res       Date:  2003-06       Impact factor: 1.886

4.  Interactions between target location and reward size modulate the rate of microsaccades in monkeys.

Authors:  Mati Joshua; Stefanie Tokiyama; Stephen G Lisberger
Journal:  J Neurophysiol       Date:  2015-08-26       Impact factor: 2.714

5.  Further evidence for selective difficulty of upward eye pursuit in juvenile monkeys: Effects of optokinetic stimulation, static roll tilt, and active head movements.

Authors:  Satoshi Kasahara; Teppei Akao; Junko Fukushima; Sergei Kurkin; Kikuro Fukushima
Journal:  Exp Brain Res       Date:  2005-11-30       Impact factor: 1.972

6.  Neuronal responses in MST reflect the post-saccadic enhancement of short-latency ocular following responses.

Authors:  Aya Takemura; Kenji Kawano
Journal:  Exp Brain Res       Date:  2006-06-29       Impact factor: 1.972

7.  The effects of preceding moving stimuli on the initial part of smooth pursuit eye movement.

Authors:  Masakatsu Taki; Kenichiro Miura; Hiromitsu Tabata; Yasuo Hisa; Kenji Kawano
Journal:  Exp Brain Res       Date:  2006-06-09       Impact factor: 1.972

8.  Deficits in short-latency tracking eye movements after chemical lesions in monkey cortical areas MT and MST.

Authors:  Aya Takemura; Yumi Murata; Kenji Kawano; F A Miles
Journal:  J Neurosci       Date:  2007-01-17       Impact factor: 6.167

9.  The effects of prolonged viewing of motion on short-latency ocular following responses.

Authors:  Masakatsu Taki; Kenichiro Miura; Hiromitsu Tabata; Yasuo Hisa; Kenji Kawano
Journal:  Exp Brain Res       Date:  2009-03-24       Impact factor: 1.972

10.  Spatial and temporal integration of visual motion signals for smooth pursuit eye movements in monkeys.

Authors:  Leslie C Osborne; Stephen G Lisberger
Journal:  J Neurophysiol       Date:  2009-08-05       Impact factor: 2.714

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