# Mechanistic explanation of neuroplasticity using equivalent circuits

**Authors:** Martin N. P. Nilsson

PMC · DOI: 10.3389/fncom.2026.1716559 · Frontiers in Computational Neuroscience · 2026-02-13

## TL;DR

This paper explains how neurons process and store information using a detailed model that combines biology and electronics concepts.

## Contribution

The paper introduces a biologically accurate neuron model that integrates Hebbian and homeostatic plasticity with a simple learning rule.

## Key findings

- The model shows neurons function as adaptive filters with internal feedback.
- Simulations confirm the model's stability and ability to learn from zero synaptic weights.
- The model captures key biological neuron characteristics missed by other models.

## Abstract

This paper presents a comprehensive mechanistic model of a neuron with plasticity that explains how information input as time-varying signals is processed and stored. Additionally, the model addresses two long-standing, specific biological challenges: Integrating Hebbian and homeostatic plasticity, and identifying a concise synaptic learning rule.

A biologically accurate small-signal equivalent-circuit model is derived through a one-to-one mapping from established ion-channel properties. The often-overlooked dynamics of the synaptic cleft is essential in this process. Analysis of the model reveals a simple and succinct learning rule, indicating that the neuron functions as an internal-feedback adaptive filter, a common concept in signal processing.

Simulations confirm the model's functionality, stability, and convergence, demonstrating that even a single neuron without external feedback can act as a potent signal processor. The model replicates several key characteristics typical of biological neurons, which are seldom captured in other neuron models. It can encode time-varying functions, learn without risking instability, and bootstrap from a state where all synaptic weights are zero.

This paper explores the function of neurons with a focus on biological accuracy, not computational efficiency. Unlike neuromorphic models, it does not aim to design devices. The electronic circuit analogy aids understanding by leveraging decades of electronics expertise but is not intended for physical implementation. This interdisciplinary work spans a broad range of subjects within the realm of neurobiophysics, including neurobiology, electronics, and signal processing.

## Full-text entities

- **Genes:** Grin1 (glutamate receptor, ionotropic, NMDA1 (zeta 1)) [NCBI Gene 14810] {aka GluN1, GluRdelta1, GluRzeta1, M100174, NMD-R1, NMDAR1}, Rhd (Rh blood group, D antigen) [NCBI Gene 19746] {aka Rh, Rhced, Rhl1}, Ier2 (immediate early response 2) [NCBI Gene 15936] {aka Ch1, Pip92}, Car5a (carbonic anhydrase 5a, mitochondrial) [NCBI Gene 12352] {aka CAV, Ca5a, Car5}, Gabrg2 (gamma-aminobutyric acid type A receptor, subunit gamma 2) [NCBI Gene 14406] {aka GABAA-R, Gabrg-2, gamma2}, Gabrg1 (gamma-aminobutyric acid type A receptor subunit gamma 1) [NCBI Gene 14405] {aka GabaA, GabaA/BZ}
- **Diseases:** NMDARs (MESH:D060426), depression (MESH:D003866)
- **Chemicals:** chloride (MESH:D002712), noradrenaline (MESH:D009638), gamma-aminobutyric acid (MESH:D005680), NMDA (MESH:D016202), Glutamate (MESH:D018698), magnesium (MESH:D008274), Ca (MESH:D002118), potassium (MESH:D011188), Na+ (MESH:D012964), Ca2+ (-), Cl- (MESH:D002713)
- **Species:** Mus musculus (house mouse, species) [taxon 10090]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12946124/full.md

## Figures

12 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12946124/full.md

## References

87 references — full list in the complete paper: https://tomesphere.com/paper/PMC12946124/full.md

---
Source: https://tomesphere.com/paper/PMC12946124