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Cerebellar learning using perturbations
The cerebellum aids the learning of fast, coordinated movements. According to current consensus, erroneously active parallel fibre synapses are depressed by complex spikes signalling movement errors. However, this theory cannot solve the credit assignment problem of processing a global movement eval...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6231762/ https://www.ncbi.nlm.nih.gov/pubmed/30418871 http://dx.doi.org/10.7554/eLife.31599 |
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author | Bouvier, Guy Aljadeff, Johnatan Clopath, Claudia Bimbard, Célian Ranft, Jonas Blot, Antonin Nadal, Jean-Pierre Brunel, Nicolas Hakim, Vincent Barbour, Boris |
author_facet | Bouvier, Guy Aljadeff, Johnatan Clopath, Claudia Bimbard, Célian Ranft, Jonas Blot, Antonin Nadal, Jean-Pierre Brunel, Nicolas Hakim, Vincent Barbour, Boris |
author_sort | Bouvier, Guy |
collection | PubMed |
description | The cerebellum aids the learning of fast, coordinated movements. According to current consensus, erroneously active parallel fibre synapses are depressed by complex spikes signalling movement errors. However, this theory cannot solve the credit assignment problem of processing a global movement evaluation into multiple cell-specific error signals. We identify a possible implementation of an algorithm solving this problem, whereby spontaneous complex spikes perturb ongoing movements, create eligibility traces and signal error changes guiding plasticity. Error changes are extracted by adaptively cancelling the average error. This framework, stochastic gradient descent with estimated global errors (SGDEGE), predicts synaptic plasticity rules that apparently contradict the current consensus but were supported by plasticity experiments in slices from mice under conditions designed to be physiological, highlighting the sensitivity of plasticity studies to experimental conditions. We analyse the algorithm’s convergence and capacity. Finally, we suggest SGDEGE may also operate in the basal ganglia. |
format | Online Article Text |
id | pubmed-6231762 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-62317622018-11-16 Cerebellar learning using perturbations Bouvier, Guy Aljadeff, Johnatan Clopath, Claudia Bimbard, Célian Ranft, Jonas Blot, Antonin Nadal, Jean-Pierre Brunel, Nicolas Hakim, Vincent Barbour, Boris eLife Neuroscience The cerebellum aids the learning of fast, coordinated movements. According to current consensus, erroneously active parallel fibre synapses are depressed by complex spikes signalling movement errors. However, this theory cannot solve the credit assignment problem of processing a global movement evaluation into multiple cell-specific error signals. We identify a possible implementation of an algorithm solving this problem, whereby spontaneous complex spikes perturb ongoing movements, create eligibility traces and signal error changes guiding plasticity. Error changes are extracted by adaptively cancelling the average error. This framework, stochastic gradient descent with estimated global errors (SGDEGE), predicts synaptic plasticity rules that apparently contradict the current consensus but were supported by plasticity experiments in slices from mice under conditions designed to be physiological, highlighting the sensitivity of plasticity studies to experimental conditions. We analyse the algorithm’s convergence and capacity. Finally, we suggest SGDEGE may also operate in the basal ganglia. eLife Sciences Publications, Ltd 2018-11-12 /pmc/articles/PMC6231762/ /pubmed/30418871 http://dx.doi.org/10.7554/eLife.31599 Text en © 2018, Bouvier et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Neuroscience Bouvier, Guy Aljadeff, Johnatan Clopath, Claudia Bimbard, Célian Ranft, Jonas Blot, Antonin Nadal, Jean-Pierre Brunel, Nicolas Hakim, Vincent Barbour, Boris Cerebellar learning using perturbations |
title | Cerebellar learning using perturbations |
title_full | Cerebellar learning using perturbations |
title_fullStr | Cerebellar learning using perturbations |
title_full_unstemmed | Cerebellar learning using perturbations |
title_short | Cerebellar learning using perturbations |
title_sort | cerebellar learning using perturbations |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6231762/ https://www.ncbi.nlm.nih.gov/pubmed/30418871 http://dx.doi.org/10.7554/eLife.31599 |
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