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Learning of Precise Spike Times with Homeostatic Membrane Potential Dependent Synaptic Plasticity

Precise spatio-temporal patterns of neuronal action potentials underly e.g. sensory representations and control of muscle activities. However, it is not known how the synaptic efficacies in the neuronal networks of the brain adapt such that they can reliably generate spikes at specific points in tim...

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Detalles Bibliográficos
Autores principales: Albers, Christian, Westkott, Maren, Pawelzik, Klaus
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4763343/
https://www.ncbi.nlm.nih.gov/pubmed/26900845
http://dx.doi.org/10.1371/journal.pone.0148948
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author Albers, Christian
Westkott, Maren
Pawelzik, Klaus
author_facet Albers, Christian
Westkott, Maren
Pawelzik, Klaus
author_sort Albers, Christian
collection PubMed
description Precise spatio-temporal patterns of neuronal action potentials underly e.g. sensory representations and control of muscle activities. However, it is not known how the synaptic efficacies in the neuronal networks of the brain adapt such that they can reliably generate spikes at specific points in time. Existing activity-dependent plasticity rules like Spike-Timing-Dependent Plasticity are agnostic to the goal of learning spike times. On the other hand, the existing formal and supervised learning algorithms perform a temporally precise comparison of projected activity with the target, but there is no known biologically plausible implementation of this comparison. Here, we propose a simple and local unsupervised synaptic plasticity mechanism that is derived from the requirement of a balanced membrane potential. Since the relevant signal for synaptic change is the postsynaptic voltage rather than spike times, we call the plasticity rule Membrane Potential Dependent Plasticity (MPDP). Combining our plasticity mechanism with spike after-hyperpolarization causes a sensitivity of synaptic change to pre- and postsynaptic spike times which can reproduce Hebbian spike timing dependent plasticity for inhibitory synapses as was found in experiments. In addition, the sensitivity of MPDP to the time course of the voltage when generating a spike allows MPDP to distinguish between weak (spurious) and strong (teacher) spikes, which therefore provides a neuronal basis for the comparison of actual and target activity. For spatio-temporal input spike patterns our conceptually simple plasticity rule achieves a surprisingly high storage capacity for spike associations. The sensitivity of the MPDP to the subthreshold membrane potential during training allows robust memory retrieval after learning even in the presence of activity corrupted by noise. We propose that MPDP represents a biophysically plausible mechanism to learn temporal target activity patterns.
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spelling pubmed-47633432016-03-07 Learning of Precise Spike Times with Homeostatic Membrane Potential Dependent Synaptic Plasticity Albers, Christian Westkott, Maren Pawelzik, Klaus PLoS One Research Article Precise spatio-temporal patterns of neuronal action potentials underly e.g. sensory representations and control of muscle activities. However, it is not known how the synaptic efficacies in the neuronal networks of the brain adapt such that they can reliably generate spikes at specific points in time. Existing activity-dependent plasticity rules like Spike-Timing-Dependent Plasticity are agnostic to the goal of learning spike times. On the other hand, the existing formal and supervised learning algorithms perform a temporally precise comparison of projected activity with the target, but there is no known biologically plausible implementation of this comparison. Here, we propose a simple and local unsupervised synaptic plasticity mechanism that is derived from the requirement of a balanced membrane potential. Since the relevant signal for synaptic change is the postsynaptic voltage rather than spike times, we call the plasticity rule Membrane Potential Dependent Plasticity (MPDP). Combining our plasticity mechanism with spike after-hyperpolarization causes a sensitivity of synaptic change to pre- and postsynaptic spike times which can reproduce Hebbian spike timing dependent plasticity for inhibitory synapses as was found in experiments. In addition, the sensitivity of MPDP to the time course of the voltage when generating a spike allows MPDP to distinguish between weak (spurious) and strong (teacher) spikes, which therefore provides a neuronal basis for the comparison of actual and target activity. For spatio-temporal input spike patterns our conceptually simple plasticity rule achieves a surprisingly high storage capacity for spike associations. The sensitivity of the MPDP to the subthreshold membrane potential during training allows robust memory retrieval after learning even in the presence of activity corrupted by noise. We propose that MPDP represents a biophysically plausible mechanism to learn temporal target activity patterns. Public Library of Science 2016-02-22 /pmc/articles/PMC4763343/ /pubmed/26900845 http://dx.doi.org/10.1371/journal.pone.0148948 Text en © 2016 Albers et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Albers, Christian
Westkott, Maren
Pawelzik, Klaus
Learning of Precise Spike Times with Homeostatic Membrane Potential Dependent Synaptic Plasticity
title Learning of Precise Spike Times with Homeostatic Membrane Potential Dependent Synaptic Plasticity
title_full Learning of Precise Spike Times with Homeostatic Membrane Potential Dependent Synaptic Plasticity
title_fullStr Learning of Precise Spike Times with Homeostatic Membrane Potential Dependent Synaptic Plasticity
title_full_unstemmed Learning of Precise Spike Times with Homeostatic Membrane Potential Dependent Synaptic Plasticity
title_short Learning of Precise Spike Times with Homeostatic Membrane Potential Dependent Synaptic Plasticity
title_sort learning of precise spike times with homeostatic membrane potential dependent synaptic plasticity
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4763343/
https://www.ncbi.nlm.nih.gov/pubmed/26900845
http://dx.doi.org/10.1371/journal.pone.0148948
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