Inverse stochastic resonance in networks of spiking neurons.

PLoS Comput Biol

Department of Electromagnetism and Physics of Matter, and Institute Carlos I for Theoretical and Computational Physics, University of Granada, Granada, Spain.

Published: July 2017

AI Article Synopsis

  • Inverse Stochastic Resonance (ISR) shows that a neuron's average spiking rate can reach a minimum when noise is present, and this study explores ISR in scale-free networks.
  • The research employs Hodgkin-Huxley model neurons with channel noise and examines how network connections, like gap junctions and synapses, affect ISR.
  • Findings indicate that weak connectivity enhances ISR under certain conditions, especially highlighting that network structure plays a crucial role in the neuron's response to noise, which could inform experimental observations of ISR in real neuronal systems.

Article Abstract

Inverse Stochastic Resonance (ISR) is a phenomenon in which the average spiking rate of a neuron exhibits a minimum with respect to noise. ISR has been studied in individual neurons, but here, we investigate ISR in scale-free networks, where the average spiking rate is calculated over the neuronal population. We use Hodgkin-Huxley model neurons with channel noise (i.e., stochastic gating variable dynamics), and the network connectivity is implemented via electrical or chemical connections (i.e., gap junctions or excitatory/inhibitory synapses). We find that the emergence of ISR depends on the interplay between each neuron's intrinsic dynamical structure, channel noise, and network inputs, where the latter in turn depend on network structure parameters. We observe that with weak gap junction or excitatory synaptic coupling, network heterogeneity and sparseness tend to favor the emergence of ISR. With inhibitory coupling, ISR is quite robust. We also identify dynamical mechanisms that underlie various features of this ISR behavior. Our results suggest possible ways of experimentally observing ISR in actual neuronal systems.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5524418PMC
http://dx.doi.org/10.1371/journal.pcbi.1005646DOI Listing

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