Literature DB >> 16033945

Distinct patterns of stimulus generalization of increases and decreases in VOR gain.

Rhea R Kimpo1, Edward S Boyden, Akira Katoh, Michael C Ke, Jennifer L Raymond.   

Abstract

Motor learning must be capable of increasing or decreasing the amplitude of movements to meet the demands of the environment. One way to implement such opposite learned changes would be to store them with bidirectional plasticity mechanisms (i.e., long-term potentiation and depression at the same synapses). At the behavioral level, this scheme should result in similar patterns of stimulus generalization of increases and decreases in movement amplitude because the same synapses would be modified but in opposite directions. To test this idea, we quantitatively compared the stimulus generalization of learned increases and decreases in the gain (amplitude) of the vestibuloocular reflex (VOR) in mice and in monkeys. When examined across different sinusoidal frequencies of head rotation, decreases in VOR gain generalized more than increases in gain. This difference was apparent not only in the gain, but also the phase (timing) of the VOR. Furthermore, this difference held when animals were trained with high-frequency rotational stimuli, a manipulation that enhances frequency generalization. Our results suggest that increases and decreases in VOR gain are not exact inverses at the circuit level. At one or more sites, the plasticity mechanisms supporting decreases in VOR gain must be less synapse-specific, or affect neurons more broadly tuned for head rotation frequency, than the mechanisms supporting increases in gain.

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Year:  2005        PMID: 16033945     DOI: 10.1152/jn.00048.2005

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


  26 in total

1.  Modeling spatial tuning of adaptation of the angular vestibulo-ocular reflex.

Authors:  Yongqing Xiang; Sergei B Yakushin; Theodore Raphan
Journal:  Exp Brain Res       Date:  2012-06-04       Impact factor: 1.972

2.  Tuning of gravity-dependent and gravity-independent vertical angular VOR gain changes by frequency of adaptation.

Authors:  Sergei B Yakushin
Journal:  J Neurophysiol       Date:  2012-03-07       Impact factor: 2.714

3.  Lock-and-key mechanisms of cerebellar memory recall based on rebound currents.

Authors:  Daniel Z Wetmore; Eran A Mukamel; Mark J Schnitzer
Journal:  J Neurophysiol       Date:  2007-08-01       Impact factor: 2.714

4.  Impaired motor learning in the vestibulo-ocular reflex in mice with multiple climbing fiber input to cerebellar Purkinje cells.

Authors:  Rhea R Kimpo; Jennifer L Raymond
Journal:  J Neurosci       Date:  2007-05-23       Impact factor: 6.167

5.  Adaptive-filter models of the cerebellum: computational analysis.

Authors:  Paul Dean; John Porrill
Journal:  Cerebellum       Date:  2008       Impact factor: 3.847

Review 6.  Motor learning in the VOR: the cerebellar component.

Authors:  Dianne M Broussard; Heather K Titley; Jordan Antflick; David R Hampson
Journal:  Exp Brain Res       Date:  2011-02-19       Impact factor: 1.972

7.  Multiple timescales in the adaptation of the rotational VOR.

Authors:  Paolo Colagiorgio; Giovanni Bertolini; Christopher J Bockisch; Dominik Straumann; Stefano Ramat
Journal:  J Neurophysiol       Date:  2015-03-04       Impact factor: 2.714

8.  Signals and learning rules guiding oculomotor plasticity.

Authors:  Soon-Lim Shin; Grace Q Zhao; Jennifer L Raymond
Journal:  J Neurosci       Date:  2014-08-06       Impact factor: 6.167

Review 9.  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

10.  Long-term size-increasing adaptation of saccades in macaques.

Authors:  A L Mueller; A J Davis; F R Robinson
Journal:  Neuroscience       Date:  2012-08-17       Impact factor: 3.590

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