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A memristive model of spatio-temporal excitability

Thomas SJ Burger, Amir Shahhosseini, Rodolphe Sepulchre

TL;DR

The paper addresses the challenge of modeling neuronal excitability across disparate scales by proposing a memristive framework that unifies temporal and spatial mechanisms. By retaining the Hodgkin–Huxley circuit structure and Amari's neural-field ideas while introducing memductances that depend on the history of the field, the authors present a single, cross-scale mechanism capable of capturing both cellular and population dynamics. They demonstrate temporal excitability via a fast-acting memductance with rapid positive feedback and slower negative feedback, and spatial excitability via short-range excitation with longer-range inhibition, all cast within a memristive, CNN-like operator framework. The resulting spatio-temporal model preserves biophysical interpretability, supports scalable simulations, and offers a pathway to extend excitability to more complex behaviors such as bursting, with potential implications for neuromorphic design and cross-scale neuroscience analysis.

Abstract

This paper introduces a model of excitability that unifies the mechanism of an important neuronal property both in time and in space. As a starting point, we revisit both a key model of temporal excitability, proposed by Hodgkin and Huxley, and a key model of spatial excitability, proposed by Amari. We then propose a novel model that captures the temporal and spatial properties of both models. Our aim is to regard neuronal excitability as a property across scales, and to explore the benefits of modeling excitability with one and the same mechanism, whether at the cellular or the population level.

A memristive model of spatio-temporal excitability

TL;DR

The paper addresses the challenge of modeling neuronal excitability across disparate scales by proposing a memristive framework that unifies temporal and spatial mechanisms. By retaining the Hodgkin–Huxley circuit structure and Amari's neural-field ideas while introducing memductances that depend on the history of the field, the authors present a single, cross-scale mechanism capable of capturing both cellular and population dynamics. They demonstrate temporal excitability via a fast-acting memductance with rapid positive feedback and slower negative feedback, and spatial excitability via short-range excitation with longer-range inhibition, all cast within a memristive, CNN-like operator framework. The resulting spatio-temporal model preserves biophysical interpretability, supports scalable simulations, and offers a pathway to extend excitability to more complex behaviors such as bursting, with potential implications for neuromorphic design and cross-scale neuroscience analysis.

Abstract

This paper introduces a model of excitability that unifies the mechanism of an important neuronal property both in time and in space. As a starting point, we revisit both a key model of temporal excitability, proposed by Hodgkin and Huxley, and a key model of spatial excitability, proposed by Amari. We then propose a novel model that captures the temporal and spatial properties of both models. Our aim is to regard neuronal excitability as a property across scales, and to explore the benefits of modeling excitability with one and the same mechanism, whether at the cellular or the population level.

Paper Structure

This paper contains 12 sections, 11 equations, 9 figures, 5 tables.

Figures (9)

  • Figure 1: Temporal excitability in the Hodgkin-Huxley model. A small difference in $i_\text{app}$ (bottom) can cause a large difference in the voltage response (top).
  • Figure 2: Block diagram of the mixed temporal monotone structure of the Hodgkin-Huxley model.
  • Figure 3: Sketch of $w(x)$ as used in Amari's model.
  • Figure 4: Spatial excitability in Amari's model. Left: the subthreshold steady-state voltage response $u^{ss}(x)$ (top) to Gaussian input current (bottom). Right: The superthreshold steady-state voltage response $u^{ss}(x)$ (top) to a Gaussian input current (bottom). The first applied pulse does not lead to spatial excitation, whereas the second applied pulse does,
  • Figure 5: Block diagram of the mixed spatial monotone structure of Amari's model. We require $\sigma_E < \sigma_I$ to ensure that the excitatory interactions given by $i_E$ operate on shorter length scales than the inhibitory interactions given by $i_I$.
  • ...and 4 more figures