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Homeostatic Plasticity Achieved by Incorporation of Random Fluctuations and Soft-Bounded Hebbian Plasticity in Excitatory Synapses
Homeostatic plasticity is considered to maintain activity in neuronal circuits within a functional range. In the absence of homeostatic plasticity neuronal activity is prone to be destabilized because Hebbian plasticity mechanisms induce positive feedback change. Several studies on homeostatic plast...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2016
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4887490/ https://www.ncbi.nlm.nih.gov/pubmed/27313513 http://dx.doi.org/10.3389/fncir.2016.00042 |
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author | Matsubara, Takashi Uehara, Kuniaki |
author_facet | Matsubara, Takashi Uehara, Kuniaki |
author_sort | Matsubara, Takashi |
collection | PubMed |
description | Homeostatic plasticity is considered to maintain activity in neuronal circuits within a functional range. In the absence of homeostatic plasticity neuronal activity is prone to be destabilized because Hebbian plasticity mechanisms induce positive feedback change. Several studies on homeostatic plasticity assumed the existence of a process for monitoring neuronal activity on a time scale of hours and adjusting synaptic efficacy by scaling up and down. However, the underlying mechanism still remains unclear. Excitatory synaptic efficacy is associated with the size of the dendritic spine, and dendritic spine size fluctuates even after neuronal activity is silenced. These fluctuations could be a non-Hebbian form of synaptic plasticity that serves such a homeostatic function. This study proposed and analyzed a synaptic plasticity model incorporating random fluctuations and soft-bounded Hebbian plasticity at excitatory synapses, and found that the proposed model can prevent excessive changes in neuronal activity by scaling synaptic efficacy up and down. Soft-bounded Hebbian plasticity suppresses strong synapses, thereby scaling synapses down and preventing runaway excitation. Random fluctuations diffuse synaptic efficacy, thereby scaling synapses up and preventing neurons from falling silent. The proposed model acts as a form of homeostatic plasticity, regardless of neuronal activity monitoring. |
format | Online Article Text |
id | pubmed-4887490 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-48874902016-06-16 Homeostatic Plasticity Achieved by Incorporation of Random Fluctuations and Soft-Bounded Hebbian Plasticity in Excitatory Synapses Matsubara, Takashi Uehara, Kuniaki Front Neural Circuits Neuroscience Homeostatic plasticity is considered to maintain activity in neuronal circuits within a functional range. In the absence of homeostatic plasticity neuronal activity is prone to be destabilized because Hebbian plasticity mechanisms induce positive feedback change. Several studies on homeostatic plasticity assumed the existence of a process for monitoring neuronal activity on a time scale of hours and adjusting synaptic efficacy by scaling up and down. However, the underlying mechanism still remains unclear. Excitatory synaptic efficacy is associated with the size of the dendritic spine, and dendritic spine size fluctuates even after neuronal activity is silenced. These fluctuations could be a non-Hebbian form of synaptic plasticity that serves such a homeostatic function. This study proposed and analyzed a synaptic plasticity model incorporating random fluctuations and soft-bounded Hebbian plasticity at excitatory synapses, and found that the proposed model can prevent excessive changes in neuronal activity by scaling synaptic efficacy up and down. Soft-bounded Hebbian plasticity suppresses strong synapses, thereby scaling synapses down and preventing runaway excitation. Random fluctuations diffuse synaptic efficacy, thereby scaling synapses up and preventing neurons from falling silent. The proposed model acts as a form of homeostatic plasticity, regardless of neuronal activity monitoring. Frontiers Media S.A. 2016-06-01 /pmc/articles/PMC4887490/ /pubmed/27313513 http://dx.doi.org/10.3389/fncir.2016.00042 Text en Copyright © 2016 Matsubara and Uehara. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Neuroscience Matsubara, Takashi Uehara, Kuniaki Homeostatic Plasticity Achieved by Incorporation of Random Fluctuations and Soft-Bounded Hebbian Plasticity in Excitatory Synapses |
title | Homeostatic Plasticity Achieved by Incorporation of Random Fluctuations and Soft-Bounded Hebbian Plasticity in Excitatory Synapses |
title_full | Homeostatic Plasticity Achieved by Incorporation of Random Fluctuations and Soft-Bounded Hebbian Plasticity in Excitatory Synapses |
title_fullStr | Homeostatic Plasticity Achieved by Incorporation of Random Fluctuations and Soft-Bounded Hebbian Plasticity in Excitatory Synapses |
title_full_unstemmed | Homeostatic Plasticity Achieved by Incorporation of Random Fluctuations and Soft-Bounded Hebbian Plasticity in Excitatory Synapses |
title_short | Homeostatic Plasticity Achieved by Incorporation of Random Fluctuations and Soft-Bounded Hebbian Plasticity in Excitatory Synapses |
title_sort | homeostatic plasticity achieved by incorporation of random fluctuations and soft-bounded hebbian plasticity in excitatory synapses |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4887490/ https://www.ncbi.nlm.nih.gov/pubmed/27313513 http://dx.doi.org/10.3389/fncir.2016.00042 |
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