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Mesoscopic description of hippocampal replay and metastability in spiking neural networks with short-term plasticity

Bottom-up models of functionally relevant patterns of neural activity provide an explicit link between neuronal dynamics and computation. A prime example of functional activity patterns are propagating bursts of place-cell activities called hippocampal replay, which is critical for memory consolidat...

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Autores principales: Pietras, Bastian, Schmutz, Valentin, Schwalger, Tilo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9822116/
https://www.ncbi.nlm.nih.gov/pubmed/36548392
http://dx.doi.org/10.1371/journal.pcbi.1010809
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author Pietras, Bastian
Schmutz, Valentin
Schwalger, Tilo
author_facet Pietras, Bastian
Schmutz, Valentin
Schwalger, Tilo
author_sort Pietras, Bastian
collection PubMed
description Bottom-up models of functionally relevant patterns of neural activity provide an explicit link between neuronal dynamics and computation. A prime example of functional activity patterns are propagating bursts of place-cell activities called hippocampal replay, which is critical for memory consolidation. The sudden and repeated occurrences of these burst states during ongoing neural activity suggest metastable neural circuit dynamics. As metastability has been attributed to noise and/or slow fatigue mechanisms, we propose a concise mesoscopic model which accounts for both. Crucially, our model is bottom-up: it is analytically derived from the dynamics of finite-size networks of Linear-Nonlinear Poisson neurons with short-term synaptic depression. As such, noise is explicitly linked to stochastic spiking and network size, and fatigue is explicitly linked to synaptic dynamics. To derive the mesoscopic model, we first consider a homogeneous spiking neural network and follow the temporal coarse-graining approach of Gillespie to obtain a “chemical Langevin equation”, which can be naturally interpreted as a stochastic neural mass model. The Langevin equation is computationally inexpensive to simulate and enables a thorough study of metastable dynamics in classical setups (population spikes and Up-Down-states dynamics) by means of phase-plane analysis. An extension of the Langevin equation for small network sizes is also presented. The stochastic neural mass model constitutes the basic component of our mesoscopic model for replay. We show that the mesoscopic model faithfully captures the statistical structure of individual replayed trajectories in microscopic simulations and in previously reported experimental data. Moreover, compared to the deterministic Romani-Tsodyks model of place-cell dynamics, it exhibits a higher level of variability regarding order, direction and timing of replayed trajectories, which seems biologically more plausible and could be functionally desirable. This variability is the product of a new dynamical regime where metastability emerges from a complex interplay between finite-size fluctuations and local fatigue.
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spelling pubmed-98221162023-01-07 Mesoscopic description of hippocampal replay and metastability in spiking neural networks with short-term plasticity Pietras, Bastian Schmutz, Valentin Schwalger, Tilo PLoS Comput Biol Research Article Bottom-up models of functionally relevant patterns of neural activity provide an explicit link between neuronal dynamics and computation. A prime example of functional activity patterns are propagating bursts of place-cell activities called hippocampal replay, which is critical for memory consolidation. The sudden and repeated occurrences of these burst states during ongoing neural activity suggest metastable neural circuit dynamics. As metastability has been attributed to noise and/or slow fatigue mechanisms, we propose a concise mesoscopic model which accounts for both. Crucially, our model is bottom-up: it is analytically derived from the dynamics of finite-size networks of Linear-Nonlinear Poisson neurons with short-term synaptic depression. As such, noise is explicitly linked to stochastic spiking and network size, and fatigue is explicitly linked to synaptic dynamics. To derive the mesoscopic model, we first consider a homogeneous spiking neural network and follow the temporal coarse-graining approach of Gillespie to obtain a “chemical Langevin equation”, which can be naturally interpreted as a stochastic neural mass model. The Langevin equation is computationally inexpensive to simulate and enables a thorough study of metastable dynamics in classical setups (population spikes and Up-Down-states dynamics) by means of phase-plane analysis. An extension of the Langevin equation for small network sizes is also presented. The stochastic neural mass model constitutes the basic component of our mesoscopic model for replay. We show that the mesoscopic model faithfully captures the statistical structure of individual replayed trajectories in microscopic simulations and in previously reported experimental data. Moreover, compared to the deterministic Romani-Tsodyks model of place-cell dynamics, it exhibits a higher level of variability regarding order, direction and timing of replayed trajectories, which seems biologically more plausible and could be functionally desirable. This variability is the product of a new dynamical regime where metastability emerges from a complex interplay between finite-size fluctuations and local fatigue. Public Library of Science 2022-12-22 /pmc/articles/PMC9822116/ /pubmed/36548392 http://dx.doi.org/10.1371/journal.pcbi.1010809 Text en © 2022 Pietras et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://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
Pietras, Bastian
Schmutz, Valentin
Schwalger, Tilo
Mesoscopic description of hippocampal replay and metastability in spiking neural networks with short-term plasticity
title Mesoscopic description of hippocampal replay and metastability in spiking neural networks with short-term plasticity
title_full Mesoscopic description of hippocampal replay and metastability in spiking neural networks with short-term plasticity
title_fullStr Mesoscopic description of hippocampal replay and metastability in spiking neural networks with short-term plasticity
title_full_unstemmed Mesoscopic description of hippocampal replay and metastability in spiking neural networks with short-term plasticity
title_short Mesoscopic description of hippocampal replay and metastability in spiking neural networks with short-term plasticity
title_sort mesoscopic description of hippocampal replay and metastability in spiking neural networks with short-term plasticity
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9822116/
https://www.ncbi.nlm.nih.gov/pubmed/36548392
http://dx.doi.org/10.1371/journal.pcbi.1010809
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