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Resonance with subthreshold oscillatory drive organizes activity and optimizes learning in neural networks

Network oscillations across and within brain areas are critical for learning and performance of memory tasks. While a large amount of work has focused on the generation of neural oscillations, their effect on neuronal populations’ spiking activity and information encoding is less known. Here, we use...

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Autores principales: Roach, James P., Pidde, Aleksandra, Katz, Eitan, Wu, Jiaxing, Ognjanovski, Nicolette, Aton, Sara J., Zochowski, Michal R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: National Academy of Sciences 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5879670/
https://www.ncbi.nlm.nih.gov/pubmed/29545273
http://dx.doi.org/10.1073/pnas.1716933115
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author Roach, James P.
Pidde, Aleksandra
Katz, Eitan
Wu, Jiaxing
Ognjanovski, Nicolette
Aton, Sara J.
Zochowski, Michal R.
author_facet Roach, James P.
Pidde, Aleksandra
Katz, Eitan
Wu, Jiaxing
Ognjanovski, Nicolette
Aton, Sara J.
Zochowski, Michal R.
author_sort Roach, James P.
collection PubMed
description Network oscillations across and within brain areas are critical for learning and performance of memory tasks. While a large amount of work has focused on the generation of neural oscillations, their effect on neuronal populations’ spiking activity and information encoding is less known. Here, we use computational modeling to demonstrate that a shift in resonance responses can interact with oscillating input to ensure that networks of neurons properly encode new information represented in external inputs to the weights of recurrent synaptic connections. Using a neuronal network model, we find that due to an input current-dependent shift in their resonance response, individual neurons in a network will arrange their phases of firing to represent varying strengths of their respective inputs. As networks encode information, neurons fire more synchronously, and this effect limits the extent to which further “learning” (in the form of changes in synaptic strength) can occur. We also demonstrate that sequential patterns of neuronal firing can be accurately stored in the network; these sequences are later reproduced without external input (in the context of subthreshold oscillations) in both the forward and reverse directions (as has been observed following learning in vivo). To test whether a similar mechanism could act in vivo, we show that periodic stimulation of hippocampal neurons coordinates network activity and functional connectivity in a frequency-dependent manner. We conclude that resonance with subthreshold oscillations provides a plausible network-level mechanism to accurately encode and retrieve information without overstrengthening connections between neurons.
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spelling pubmed-58796702018-04-03 Resonance with subthreshold oscillatory drive organizes activity and optimizes learning in neural networks Roach, James P. Pidde, Aleksandra Katz, Eitan Wu, Jiaxing Ognjanovski, Nicolette Aton, Sara J. Zochowski, Michal R. Proc Natl Acad Sci U S A PNAS Plus Network oscillations across and within brain areas are critical for learning and performance of memory tasks. While a large amount of work has focused on the generation of neural oscillations, their effect on neuronal populations’ spiking activity and information encoding is less known. Here, we use computational modeling to demonstrate that a shift in resonance responses can interact with oscillating input to ensure that networks of neurons properly encode new information represented in external inputs to the weights of recurrent synaptic connections. Using a neuronal network model, we find that due to an input current-dependent shift in their resonance response, individual neurons in a network will arrange their phases of firing to represent varying strengths of their respective inputs. As networks encode information, neurons fire more synchronously, and this effect limits the extent to which further “learning” (in the form of changes in synaptic strength) can occur. We also demonstrate that sequential patterns of neuronal firing can be accurately stored in the network; these sequences are later reproduced without external input (in the context of subthreshold oscillations) in both the forward and reverse directions (as has been observed following learning in vivo). To test whether a similar mechanism could act in vivo, we show that periodic stimulation of hippocampal neurons coordinates network activity and functional connectivity in a frequency-dependent manner. We conclude that resonance with subthreshold oscillations provides a plausible network-level mechanism to accurately encode and retrieve information without overstrengthening connections between neurons. National Academy of Sciences 2018-03-27 2018-03-15 /pmc/articles/PMC5879670/ /pubmed/29545273 http://dx.doi.org/10.1073/pnas.1716933115 Text en Copyright © 2018 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by-nc-nd/4.0/ This open access article is distributed under Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle PNAS Plus
Roach, James P.
Pidde, Aleksandra
Katz, Eitan
Wu, Jiaxing
Ognjanovski, Nicolette
Aton, Sara J.
Zochowski, Michal R.
Resonance with subthreshold oscillatory drive organizes activity and optimizes learning in neural networks
title Resonance with subthreshold oscillatory drive organizes activity and optimizes learning in neural networks
title_full Resonance with subthreshold oscillatory drive organizes activity and optimizes learning in neural networks
title_fullStr Resonance with subthreshold oscillatory drive organizes activity and optimizes learning in neural networks
title_full_unstemmed Resonance with subthreshold oscillatory drive organizes activity and optimizes learning in neural networks
title_short Resonance with subthreshold oscillatory drive organizes activity and optimizes learning in neural networks
title_sort resonance with subthreshold oscillatory drive organizes activity and optimizes learning in neural networks
topic PNAS Plus
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5879670/
https://www.ncbi.nlm.nih.gov/pubmed/29545273
http://dx.doi.org/10.1073/pnas.1716933115
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