4.6 Article

Computing the Local Field Potential (LFP) from Integrate-and-Fire Network Models

Journal

PLOS COMPUTATIONAL BIOLOGY
Volume 11, Issue 12, Pages -

Publisher

PUBLIC LIBRARY SCIENCE
DOI: 10.1371/journal.pcbi.1004584

Keywords

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Funding

  1. NEBIAS European project [EUFP7-ICT-611687]
  2. PRIN/HandBot Italian project [CUP: B81J12002680008, prot.: 20102YF2RY]
  3. European Commission [FP7-284553]
  4. Italian Ministry of Foreign Affairs and International Cooperation
  5. Directorate General for Country Promotion (Economy, Culture and Science)-Unit for Scientific and Technological Cooperation, via the Italy-Sweden bilateral research project on Brain network mechanisms for integration of natural tactile input patterns
  6. Danish Council for Independent Research
  7. FP7 Marie Curie Actions - COFUND [DFF - 1330-00226]
  8. EU [269921, 604102]
  9. Dynamical Systems Interdisciplinary Network, University of Copenhagen
  10. BMBF [01GQ1406]
  11. Autonomous Province of Trento
  12. Research Council of Norway (ISP-Physics)

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Leaky integrate-and-fire (LIF) network models are commonly used to study how the spiking dynamics of neural networks changes with stimuli, tasks or dynamic network states. However, neurophysiological studies in vivo often rather measure the mass activity of neuronal microcircuits with the local field potential (LFP). Given that LFPs are generated by spatially separated currents across the neuronal membrane, they cannot be computed directly from quantities defined in models of point-like LIF neurons. Here, we explore the best approximation for predicting the LFP based on standard output from point-neuron LIF networks. To search for this best LFP proxy, we compared LFP predictions from candidate proxies based on LIF network output (e.g, firing rates, membrane potentials, synaptic currents) with ground-truth LFP obtained when the LIF network synaptic input currents were injected into an analogous three-dimensional (3D) network model of multi-compartmental neurons with realistic morphology, spatial distributions of somata and synapses. We found that a specific fixed linear combination of the LIF synaptic currents provided an accurate LFP proxy, accounting for most of the variance of the LFP time course observed in the 3D network for all recording locations. This proxy performed well over a broad set of conditions, including substantial variations of the neuronal morphologies. Our results provide a simple formula for estimating the time course of the LFP from LIF network simulations in cases where a single pyramidal population dominates the LFP generation, and thereby facilitate quantitative comparison between computational models and experimental LFP recordings in vivo.

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