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Theory of optimal balance predicts and explains the amplitude and decay time of synaptic inhibition
Synaptic inhibition counterbalances excitation, but it is not known what constitutes optimal inhibition. We previously proposed that perfect balance is achieved when the peak of an excitatory postsynaptic potential (EPSP) is exactly at spike threshold, so that the slightest variation in excitation d...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5353699/ https://www.ncbi.nlm.nih.gov/pubmed/28281523 http://dx.doi.org/10.1038/ncomms14566 |
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author | Kim, Jaekyung K. Fiorillo, Christopher D. |
author_facet | Kim, Jaekyung K. Fiorillo, Christopher D. |
author_sort | Kim, Jaekyung K. |
collection | PubMed |
description | Synaptic inhibition counterbalances excitation, but it is not known what constitutes optimal inhibition. We previously proposed that perfect balance is achieved when the peak of an excitatory postsynaptic potential (EPSP) is exactly at spike threshold, so that the slightest variation in excitation determines whether a spike is generated. Using simulations, we show that the optimal inhibitory postsynaptic conductance (IPSG) increases in amplitude and decay rate as synaptic excitation increases from 1 to 800 Hz. As further proposed by theory, we show that optimal IPSG parameters can be learned through anti-Hebbian rules. Finally, we compare our theoretical optima to published experimental data from 21 types of neurons, in which rates of synaptic excitation and IPSG decay times vary by factors of about 100 (5–600 Hz) and 50 (1–50 ms), respectively. From an infinite range of possible decay times, theory predicted experimental decay times within less than a factor of 2. Across a distinct set of 15 types of neuron recorded in vivo, theory predicted the amplitude of synaptic inhibition within a factor of 1.7. Thus, the theory can explain biophysical quantities from first principles. |
format | Online Article Text |
id | pubmed-5353699 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-53536992017-04-05 Theory of optimal balance predicts and explains the amplitude and decay time of synaptic inhibition Kim, Jaekyung K. Fiorillo, Christopher D. Nat Commun Article Synaptic inhibition counterbalances excitation, but it is not known what constitutes optimal inhibition. We previously proposed that perfect balance is achieved when the peak of an excitatory postsynaptic potential (EPSP) is exactly at spike threshold, so that the slightest variation in excitation determines whether a spike is generated. Using simulations, we show that the optimal inhibitory postsynaptic conductance (IPSG) increases in amplitude and decay rate as synaptic excitation increases from 1 to 800 Hz. As further proposed by theory, we show that optimal IPSG parameters can be learned through anti-Hebbian rules. Finally, we compare our theoretical optima to published experimental data from 21 types of neurons, in which rates of synaptic excitation and IPSG decay times vary by factors of about 100 (5–600 Hz) and 50 (1–50 ms), respectively. From an infinite range of possible decay times, theory predicted experimental decay times within less than a factor of 2. Across a distinct set of 15 types of neuron recorded in vivo, theory predicted the amplitude of synaptic inhibition within a factor of 1.7. Thus, the theory can explain biophysical quantities from first principles. Nature Publishing Group 2017-03-10 /pmc/articles/PMC5353699/ /pubmed/28281523 http://dx.doi.org/10.1038/ncomms14566 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Kim, Jaekyung K. Fiorillo, Christopher D. Theory of optimal balance predicts and explains the amplitude and decay time of synaptic inhibition |
title | Theory of optimal balance predicts and explains the amplitude and decay time of synaptic inhibition |
title_full | Theory of optimal balance predicts and explains the amplitude and decay time of synaptic inhibition |
title_fullStr | Theory of optimal balance predicts and explains the amplitude and decay time of synaptic inhibition |
title_full_unstemmed | Theory of optimal balance predicts and explains the amplitude and decay time of synaptic inhibition |
title_short | Theory of optimal balance predicts and explains the amplitude and decay time of synaptic inhibition |
title_sort | theory of optimal balance predicts and explains the amplitude and decay time of synaptic inhibition |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5353699/ https://www.ncbi.nlm.nih.gov/pubmed/28281523 http://dx.doi.org/10.1038/ncomms14566 |
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