Contrasting the effects of adaptation and synaptic filtering on the timescales of dynamics in recurrent networks.

Neural activity in awake behaving animals exhibits a vast range of timescales that can be several fold larger than the membrane time constant of individual neurons. Two types of mechanisms have been proposed to explain this conundrum. One possibility is that large timescales are generated by a netwo...

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Main Authors: Manuel Beiran, Srdjan Ostojic
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2019-03-01
Series:PLoS Computational Biology
Online Access:https://doi.org/10.1371/journal.pcbi.1006893
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spelling doaj-83351897efda45b388228044cdbb3a632021-04-21T15:11:38ZengPublic Library of Science (PLoS)PLoS Computational Biology1553-734X1553-73582019-03-01153e100689310.1371/journal.pcbi.1006893Contrasting the effects of adaptation and synaptic filtering on the timescales of dynamics in recurrent networks.Manuel BeiranSrdjan OstojicNeural activity in awake behaving animals exhibits a vast range of timescales that can be several fold larger than the membrane time constant of individual neurons. Two types of mechanisms have been proposed to explain this conundrum. One possibility is that large timescales are generated by a network mechanism based on positive feedback, but this hypothesis requires fine-tuning of the strength or structure of the synaptic connections. A second possibility is that large timescales in the neural dynamics are inherited from large timescales of underlying biophysical processes, two prominent candidates being intrinsic adaptive ionic currents and synaptic transmission. How the timescales of adaptation or synaptic transmission influence the timescale of the network dynamics has however not been fully explored. To address this question, here we analyze large networks of randomly connected excitatory and inhibitory units with additional degrees of freedom that correspond to adaptation or synaptic filtering. We determine the fixed points of the systems, their stability to perturbations and the corresponding dynamical timescales. Furthermore, we apply dynamical mean field theory to study the temporal statistics of the activity in the fluctuating regime, and examine how the adaptation and synaptic timescales transfer from individual units to the whole population. Our overarching finding is that synaptic filtering and adaptation in single neurons have very different effects at the network level. Unexpectedly, the macroscopic network dynamics do not inherit the large timescale present in adaptive currents. In contrast, the timescales of network activity increase proportionally to the time constant of the synaptic filter. Altogether, our study demonstrates that the timescales of different biophysical processes have different effects on the network level, so that the slow processes within individual neurons do not necessarily induce slow activity in large recurrent neural networks.https://doi.org/10.1371/journal.pcbi.1006893
collection DOAJ
language English
format Article
sources DOAJ
author Manuel Beiran
Srdjan Ostojic
spellingShingle Manuel Beiran
Srdjan Ostojic
Contrasting the effects of adaptation and synaptic filtering on the timescales of dynamics in recurrent networks.
PLoS Computational Biology
author_facet Manuel Beiran
Srdjan Ostojic
author_sort Manuel Beiran
title Contrasting the effects of adaptation and synaptic filtering on the timescales of dynamics in recurrent networks.
title_short Contrasting the effects of adaptation and synaptic filtering on the timescales of dynamics in recurrent networks.
title_full Contrasting the effects of adaptation and synaptic filtering on the timescales of dynamics in recurrent networks.
title_fullStr Contrasting the effects of adaptation and synaptic filtering on the timescales of dynamics in recurrent networks.
title_full_unstemmed Contrasting the effects of adaptation and synaptic filtering on the timescales of dynamics in recurrent networks.
title_sort contrasting the effects of adaptation and synaptic filtering on the timescales of dynamics in recurrent networks.
publisher Public Library of Science (PLoS)
series PLoS Computational Biology
issn 1553-734X
1553-7358
publishDate 2019-03-01
description Neural activity in awake behaving animals exhibits a vast range of timescales that can be several fold larger than the membrane time constant of individual neurons. Two types of mechanisms have been proposed to explain this conundrum. One possibility is that large timescales are generated by a network mechanism based on positive feedback, but this hypothesis requires fine-tuning of the strength or structure of the synaptic connections. A second possibility is that large timescales in the neural dynamics are inherited from large timescales of underlying biophysical processes, two prominent candidates being intrinsic adaptive ionic currents and synaptic transmission. How the timescales of adaptation or synaptic transmission influence the timescale of the network dynamics has however not been fully explored. To address this question, here we analyze large networks of randomly connected excitatory and inhibitory units with additional degrees of freedom that correspond to adaptation or synaptic filtering. We determine the fixed points of the systems, their stability to perturbations and the corresponding dynamical timescales. Furthermore, we apply dynamical mean field theory to study the temporal statistics of the activity in the fluctuating regime, and examine how the adaptation and synaptic timescales transfer from individual units to the whole population. Our overarching finding is that synaptic filtering and adaptation in single neurons have very different effects at the network level. Unexpectedly, the macroscopic network dynamics do not inherit the large timescale present in adaptive currents. In contrast, the timescales of network activity increase proportionally to the time constant of the synaptic filter. Altogether, our study demonstrates that the timescales of different biophysical processes have different effects on the network level, so that the slow processes within individual neurons do not necessarily induce slow activity in large recurrent neural networks.
url https://doi.org/10.1371/journal.pcbi.1006893
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