Cerebellar learning using perturbations
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Published version
Author(s)
Type
Journal Article
Abstract
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.
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.
Date Issued
2018-11-12
Date Acceptance
2018-10-06
Citation
eLife, 2018, 7
ISSN
2050-084X
Publisher
eLife Sciences Publications Ltd
Journal / Book Title
eLife
Volume
7
Copyright Statement
© Bouvier et al. This
article is distributed under the
terms of the Creative Commons
Attribution License, which
permits unrestricted use and
redistribution provided that the
original author and source are
credited.
article is distributed under the
terms of the Creative Commons
Attribution License, which
permits unrestricted use and
redistribution provided that the
original author and source are
credited.
Identifier
http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000449729300001&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=1ba7043ffcc86c417c072aa74d649202
Subjects
Science & Technology
Life Sciences & Biomedicine
Biology
Life Sciences & Biomedicine - Other Topics
LONG-TERM DEPRESSION
PURKINJE-CELL AXONS
CUTANEOUS RECEPTIVE-FIELDS
INFERIOR OLIVARY NEURONS
COMPLEX SPIKE ACTIVITY
MOSSY FIBER EPSCS
CLIMBING FIBERS
VESTIBULOOCULAR REFLEX
BIDIRECTIONAL PLASTICITY
EYE-MOVEMENTS
Publication Status
Published
Article Number
ARTN e31599