Literature DB >> 20884765

Learning on multiple timescales in smooth pursuit eye movements.

Yan Yang1, Stephen G Lisberger.   

Abstract

We commonly think of motor learning as a gradual process that makes small, adaptive steps in a consistent direction. We now report evidence that learning in pursuit eye movements could start with large, transient short-term alterations that stoke a more gradual long-term process. Monkeys tracked a target that started moving horizontally or vertically. After 250 ms of motion had produced a preinstruction eye velocity close to target velocity, an orthogonal component of target motion created an instructive change in target direction that was randomly in one of the two directions along the orthogonal axis. The preinstruction eye velocity in each trial expressed single-trial learning as a bias toward the direction of the instruction in the prior trial. The single-trial learning was forgotten within 4 to 10 s. Two observations implied that single-trial learning was not simply cognitive anticipation. First, the magnitude of the trial-over-trial change in eye velocity depended on the ongoing eye velocity at the time of the instruction in the prior trial. Single-trial learning was negligible if the prior trial had provided a well-timed cue without evoking any preinstruction eye velocity. Second, regular alternation of the direction of the instructive target motion caused reactive rather than anticipatory trial-over-trial changes in eye velocity. Humans showed very different responses that appeared to be based on cognitive anticipation rather than learning. We suggest that single-trial learning results from a low-level learning mechanism and may be a necessary prerequisite for longer-term modifications that are more permanent.

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Year:  2010        PMID: 20884765      PMCID: PMC2997040          DOI: 10.1152/jn.00761.2010

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


  45 in total

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Authors:  P F Gilbert; W T Thach
Journal:  Brain Res       Date:  1977-06-10       Impact factor: 3.252

2.  Visual responses of Purkinje cells in the cerebellar flocculus during smooth-pursuit eye movements in monkeys. II. Complex spikes.

Authors:  L S Stone; S G Lisberger
Journal:  J Neurophysiol       Date:  1990-05       Impact factor: 2.714

3.  Visual responses of Purkinje cells in the cerebellar flocculus during smooth-pursuit eye movements in monkeys. I. Simple spikes.

Authors:  L S Stone; S G Lisberger
Journal:  J Neurophysiol       Date:  1990-05       Impact factor: 2.714

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

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Journal:  Exp Brain Res       Date:  1973       Impact factor: 1.972

6.  Deficits in visual motion processing following ibotenic acid lesions of the middle temporal visual area of the macaque monkey.

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Journal:  J Neurosci       Date:  1985-03       Impact factor: 6.167

7.  The effect of expectations on slow oculomotor control--IV. Anticipatory smooth eye movements depend on prior target motions.

Authors:  E Kowler; A J Martins; M Pavel
Journal:  Vision Res       Date:  1984       Impact factor: 1.886

8.  Cerebellar control of the vestibulo-ocular reflex--around the flocculus hypothesis.

Authors:  M Ito
Journal:  Annu Rev Neurosci       Date:  1982       Impact factor: 12.449

Review 9.  Plasticity in the vestibulo-ocular reflex: a new hypothesis.

Authors:  F A Miles; S G Lisberger
Journal:  Annu Rev Neurosci       Date:  1981       Impact factor: 12.449

10.  Role of primate flocculus during rapid behavioral modification of vestibuloocular reflex. I. Purkinje cell activity during visually guided horizontal smooth-pursuit eye movements and passive head rotation.

Authors:  S G Lisberger; A F Fuchs
Journal:  J Neurophysiol       Date:  1978-05       Impact factor: 2.714

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  28 in total

1.  Bidirectional short-term plasticity during single-trial learning of cerebellar-driven eyelid movements in mice.

Authors:  Farzaneh Najafi; Javier F Medina
Journal:  Neurobiol Learn Mem       Date:  2019-10-11       Impact factor: 2.877

2.  Responses of Purkinje cells in the oculomotor vermis of monkeys during smooth pursuit eye movements and saccades: comparison with floccular complex.

Authors:  Ramanujan T Raghavan; Stephen G Lisberger
Journal:  J Neurophysiol       Date:  2017-05-17       Impact factor: 2.714

3.  Role of plasticity at different sites across the time course of cerebellar motor learning.

Authors:  Yan Yang; Stephen G Lisberger
Journal:  J Neurosci       Date:  2014-05-21       Impact factor: 6.167

4.  Multiple components in direction learning in smooth pursuit eye movements of monkeys.

Authors:  Nathan J Hall; Yan Yang; Stephen G Lisberger
Journal:  J Neurophysiol       Date:  2018-08-01       Impact factor: 2.714

Review 5.  Depressed by Learning-Heterogeneity of the Plasticity Rules at Parallel Fiber Synapses onto Purkinje Cells.

Authors:  Aparna Suvrathan; Jennifer L Raymond
Journal:  Cerebellum       Date:  2018-12       Impact factor: 3.847

6.  Anticipatory smooth eye movements with random-dot kinematograms.

Authors:  Elio M Santos; Edinah K Gnang; Eileen Kowler
Journal:  J Vis       Date:  2012-10-01       Impact factor: 2.240

7.  Different mechanisms for modulation of the initiation and steady-state of smooth pursuit eye movements.

Authors:  Stuart Behling; Stephen G Lisberger
Journal:  J Neurophysiol       Date:  2020-02-19       Impact factor: 2.714

Review 8.  Computational Principles of Supervised Learning in the Cerebellum.

Authors:  Jennifer L Raymond; Javier F Medina
Journal:  Annu Rev Neurosci       Date:  2018-07-08       Impact factor: 12.449

9.  Timing Rules for Synaptic Plasticity Matched to Behavioral Function.

Authors:  Aparna Suvrathan; Hannah L Payne; Jennifer L Raymond
Journal:  Neuron       Date:  2016-11-10       Impact factor: 17.173

10.  Reward action in the initiation of smooth pursuit eye movements.

Authors:  Mati Joshua; Stephen G Lisberger
Journal:  J Neurosci       Date:  2012-02-22       Impact factor: 6.167

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