The Complexity of Dynamics in Small Neural Circuits

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The Complexity of Dynamics in Small Neural Circuits. / Fasoli, Diego; Cattani, Anna; Panzeri, Stefano.

In: PLOS COMPUT BIOL, Vol. 12, No. 8, 05.08.2016, p. e1004992.

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@article{b29c309cf5604d8aa50e6018c8775ff7,
title = "The Complexity of Dynamics in Small Neural Circuits",
abstract = "Mean-field approximations are a powerful tool for studying large neural networks. However, they do not describe well the behavior of networks composed of a small number of neurons. In this case, major differences between the mean-field approximation and the real behavior of the network can arise. Yet, many interesting problems in neuroscience involve the study of mesoscopic networks composed of a few tens of neurons. Nonetheless, mathematical methods that correctly describe networks of small size are still rare, and this prevents us to make progress in understanding neural dynamics at these intermediate scales. Here we develop a novel systematic analysis of the dynamics of arbitrarily small networks composed of homogeneous populations of excitatory and inhibitory firing-rate neurons. We study the local bifurcations of their neural activity with an approach that is largely analytically tractable, and we numerically determine the global bifurcations. We find that for strong inhibition these networks give rise to very complex dynamics, caused by the formation of multiple branching solutions of the neural dynamics equations that emerge through spontaneous symmetry-breaking. This qualitative change of the neural dynamics is a finite-size effect of the network, that reveals qualitative and previously unexplored differences between mesoscopic cortical circuits and their mean-field approximation. The most important consequence of spontaneous symmetry-breaking is the ability of mesoscopic networks to regulate their degree of functional heterogeneity, which is thought to help reducing the detrimental effect of noise correlations on cortical information processing.",
keywords = "Action Potentials/physiology, Computational Biology, Models, Neurological, Nerve Net/physiology, Neurons/physiology",
author = "Diego Fasoli and Anna Cattani and Stefano Panzeri",
year = "2016",
month = aug,
day = "5",
doi = "10.1371/journal.pcbi.1004992",
language = "English",
volume = "12",
pages = "e1004992",
journal = "PLOS COMPUT BIOL",
issn = "1553-734X",
publisher = "Public Library of Science",
number = "8",

}

RIS

TY - JOUR

T1 - The Complexity of Dynamics in Small Neural Circuits

AU - Fasoli, Diego

AU - Cattani, Anna

AU - Panzeri, Stefano

PY - 2016/8/5

Y1 - 2016/8/5

N2 - Mean-field approximations are a powerful tool for studying large neural networks. However, they do not describe well the behavior of networks composed of a small number of neurons. In this case, major differences between the mean-field approximation and the real behavior of the network can arise. Yet, many interesting problems in neuroscience involve the study of mesoscopic networks composed of a few tens of neurons. Nonetheless, mathematical methods that correctly describe networks of small size are still rare, and this prevents us to make progress in understanding neural dynamics at these intermediate scales. Here we develop a novel systematic analysis of the dynamics of arbitrarily small networks composed of homogeneous populations of excitatory and inhibitory firing-rate neurons. We study the local bifurcations of their neural activity with an approach that is largely analytically tractable, and we numerically determine the global bifurcations. We find that for strong inhibition these networks give rise to very complex dynamics, caused by the formation of multiple branching solutions of the neural dynamics equations that emerge through spontaneous symmetry-breaking. This qualitative change of the neural dynamics is a finite-size effect of the network, that reveals qualitative and previously unexplored differences between mesoscopic cortical circuits and their mean-field approximation. The most important consequence of spontaneous symmetry-breaking is the ability of mesoscopic networks to regulate their degree of functional heterogeneity, which is thought to help reducing the detrimental effect of noise correlations on cortical information processing.

AB - Mean-field approximations are a powerful tool for studying large neural networks. However, they do not describe well the behavior of networks composed of a small number of neurons. In this case, major differences between the mean-field approximation and the real behavior of the network can arise. Yet, many interesting problems in neuroscience involve the study of mesoscopic networks composed of a few tens of neurons. Nonetheless, mathematical methods that correctly describe networks of small size are still rare, and this prevents us to make progress in understanding neural dynamics at these intermediate scales. Here we develop a novel systematic analysis of the dynamics of arbitrarily small networks composed of homogeneous populations of excitatory and inhibitory firing-rate neurons. We study the local bifurcations of their neural activity with an approach that is largely analytically tractable, and we numerically determine the global bifurcations. We find that for strong inhibition these networks give rise to very complex dynamics, caused by the formation of multiple branching solutions of the neural dynamics equations that emerge through spontaneous symmetry-breaking. This qualitative change of the neural dynamics is a finite-size effect of the network, that reveals qualitative and previously unexplored differences between mesoscopic cortical circuits and their mean-field approximation. The most important consequence of spontaneous symmetry-breaking is the ability of mesoscopic networks to regulate their degree of functional heterogeneity, which is thought to help reducing the detrimental effect of noise correlations on cortical information processing.

KW - Action Potentials/physiology

KW - Computational Biology

KW - Models, Neurological

KW - Nerve Net/physiology

KW - Neurons/physiology

U2 - 10.1371/journal.pcbi.1004992

DO - 10.1371/journal.pcbi.1004992

M3 - SCORING: Journal article

C2 - 27494737

VL - 12

SP - e1004992

JO - PLOS COMPUT BIOL

JF - PLOS COMPUT BIOL

SN - 1553-734X

IS - 8

ER -