Evidence map›Paper›PMID 42522932›Full record

ArticleThe Journal of physiology2026

Modelling the memory of unmyelinated axons: Integration of a data-driven approach with physiological memory concept.

Anna Maxion, Jenny Tigerholm, Barbara Namer, Ekaterina Kutafina

Abstract read
In one paragraph

Article in The Journal of physiology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Anna MaxionJoint Research Center for Computational Biomedicine, Medical Faculty, RWTH Aachen University, Aachen, Germany.ORCID https://orcid.org/0009-0001-7777-6478
Jenny TigerholmJoint Research Center for Computational Biomedicine, Medical Faculty, RWTH Aachen University, Aachen, Germany.
Barbara NamerCenter for interdisciplinary pain medicine, Department of Anesthesiology, Intensive Care, Emergency and Pain Medicine, University Hospital Würzburg, Center for Interdisciplinary Pain Medicine, Würzburg, Germany.ORCID https://orcid.org/0000-0001-7500-2842
Ekaterina KutafinaInstitute for Biomedical Informatics, Faculty of Medicine and University Hospital Cologne, University of Cologne, Cologne, Germany.ORCID https://orcid.org/0000-0002-3430-5123

Funding

German Research Council DFGNA9706-2German Research Council DFGNA9707-1German Research Council DFGNA9709-2
6 · The paper itself

Abstract

This study aims to present a simplified and resource-efficient computational model for predicting activity-dependent conduction velocity changes in unmyelinated axons, serving as a complementary tool to Hodgkin-Huxley models. Our approach is based on the concept of 'memory', where the speed of action potentials is modulated by prior activity. We utilized microneurography data from 95 mechano-insensitive C-fibres of healthy human participants, including both sexes, across various stimulation protocols to optimize model parameters. The model incorporates linear long-term and non-linear short-term memory components, effectively predicting propagation speed by convolving the history of recorded action potentials with the memory function. The proposed one-dimensional and two-dimensional memory functions yielded low mean squared errors in predicting the propagation speed of subsequent action potentials. This computational framework provides insights into dynamics of unmyelinated axons under varying conditions, enhancing our understanding of signal processing along the axon and its short-term memory capabilities. Additionally our model demonstrates rapid computation times suitable for real-time applications in electrophysiological experiments. This study introduces a novel model that simulates activity-dependent conduction velocity changes in unmyelinated axons, which is crucial for effective signal processing during conduction. Unlike Hodgkin-Huxley models that are computationally intensive and complex, our approach leverages fibre 'memory' to capture how prior activity influences conduction. With fewer parameters required to fit diverse datasets, including patient data, our highly efficient model enables faster simulations than Hodgkin-Huxley models and facilitates the analysis of spike train propagation over long distances, and it is therefore suitable for modelling peripheral axons that extend up to 1 m. KEY POINTS: Unmyelinated axons, which are present in the peripheral and central nervous system, exhibit conduction velocity changes influenced by previous fibre activity, creating a form of fibre 'memory'. This study presents a novel computational model that predicts conduction velocity changes in unmyelinated axons based on prior activity, providing a faster and more efficient addition to complex Hodgkin-Huxley models. The new model incorporates both linear long-term and non-linear short-term memory components, demonstrating rapid computation times suitable for real-time applications. The model effectively captures the dynamics of nerve fibres, enhancing our understanding of axonal signal processing. This work offers insights into how previous activity influences axonal behaviour, informing future research on neurological disorders associated with altered nerve function.

Indexed as

AxonsModels, NeurologicalNerve Fibers, UnmyelinatedAction PotentialsAdultComputer SimulationFemaleHumansMaleMemoryNeural Conductionactivity‐dependent slowingcomputational modelfibre memorysignal processingunmyelinated axons

Identifiers

PMID42522932
PMCPMC13532846

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.