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Gating by Functionally Indivisible Cerebellar Circuits: a Hypothesis

The attempt to understand the cerebellum has been dominated for years by supervised learning models. The central idea is that a learning algorithm modifies transmission strength at repeatedly co-active synapses, creating memories stored as finely calibrated synaptic weights. As a result, Purkinje ce...

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Detalles Bibliográficos
Autores principales: Gilbert, Mike, Miall, Chris
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8360902/
https://www.ncbi.nlm.nih.gov/pubmed/33464470
http://dx.doi.org/10.1007/s12311-020-01223-6
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author Gilbert, Mike
Miall, Chris
author_facet Gilbert, Mike
Miall, Chris
author_sort Gilbert, Mike
collection PubMed
description The attempt to understand the cerebellum has been dominated for years by supervised learning models. The central idea is that a learning algorithm modifies transmission strength at repeatedly co-active synapses, creating memories stored as finely calibrated synaptic weights. As a result, Purkinje cells, usually the de facto output cells of these models, acquire a modified response to input in a remembered pattern. This paper proposes an alternative model of pattern memory in which the function of a match is permissive, allowing but not driving output, and accordingly controlling the timing of output but not the rate of firing by Purkinje cells. Learning does not result in graded synaptic weights. There is no supervised learning algorithm or memory of individual patterns, which, like graded weights, are unnecessary to explain the evidence. Instead, patterns are classed as simply either known or not, at the level of input to a functional population of 100s of Purkinje cells (a microzone). The standard is strict. If only a handful of Purkinje cells receive a mismatch output of the whole circuit is blocked. Only if there is a full and accurate match are projection neurons in deep nuclei, which carry the output of most circuits, released from default inhibitory restraint. Purkinje cell firing at those times is a linear function of input rates. There is no effect of modification of synaptic transmission except to either allow or block output.
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spelling pubmed-83609022021-08-30 Gating by Functionally Indivisible Cerebellar Circuits: a Hypothesis Gilbert, Mike Miall, Chris Cerebellum Original Article The attempt to understand the cerebellum has been dominated for years by supervised learning models. The central idea is that a learning algorithm modifies transmission strength at repeatedly co-active synapses, creating memories stored as finely calibrated synaptic weights. As a result, Purkinje cells, usually the de facto output cells of these models, acquire a modified response to input in a remembered pattern. This paper proposes an alternative model of pattern memory in which the function of a match is permissive, allowing but not driving output, and accordingly controlling the timing of output but not the rate of firing by Purkinje cells. Learning does not result in graded synaptic weights. There is no supervised learning algorithm or memory of individual patterns, which, like graded weights, are unnecessary to explain the evidence. Instead, patterns are classed as simply either known or not, at the level of input to a functional population of 100s of Purkinje cells (a microzone). The standard is strict. If only a handful of Purkinje cells receive a mismatch output of the whole circuit is blocked. Only if there is a full and accurate match are projection neurons in deep nuclei, which carry the output of most circuits, released from default inhibitory restraint. Purkinje cell firing at those times is a linear function of input rates. There is no effect of modification of synaptic transmission except to either allow or block output. Springer US 2021-01-19 2021 /pmc/articles/PMC8360902/ /pubmed/33464470 http://dx.doi.org/10.1007/s12311-020-01223-6 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Original Article
Gilbert, Mike
Miall, Chris
Gating by Functionally Indivisible Cerebellar Circuits: a Hypothesis
title Gating by Functionally Indivisible Cerebellar Circuits: a Hypothesis
title_full Gating by Functionally Indivisible Cerebellar Circuits: a Hypothesis
title_fullStr Gating by Functionally Indivisible Cerebellar Circuits: a Hypothesis
title_full_unstemmed Gating by Functionally Indivisible Cerebellar Circuits: a Hypothesis
title_short Gating by Functionally Indivisible Cerebellar Circuits: a Hypothesis
title_sort gating by functionally indivisible cerebellar circuits: a hypothesis
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8360902/
https://www.ncbi.nlm.nih.gov/pubmed/33464470
http://dx.doi.org/10.1007/s12311-020-01223-6
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