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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...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2016
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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. |
format | Online Article Text |
id | pubmed-4763343 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
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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