Evidence map›Paper›PMID 29948844›Full record

ArticleNeuroinformatics2019

PyPNS: Multiscale Simulation of a Peripheral Nerve in Python.

Carl H Lubba, Yann Le Guen, Sarah Jarvis, Nick S Jones, Simon C Cork, Amir Eftekhar, Simon R Schultz

Erratum issuedAbstract read
In one paragraph

Article in Neuroinformatics, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing 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

19 citing papers in PubMed.

  1. Review
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  8. Computational modeling of autonomic nerve stimulation: Vagus et al.Current opinion in biomedical engineering · 2024
    Article
  9. Article
  10. Article
  11. NRV: An open framework forbioRxiv : the preprint server for biology · 2024
    Article
  12. Article
  13. Review
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  17. Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors.

Carl H LubbaDepartment of Bioengineering, Imperial College London, South Kensington, London, SW7 2AZ, UK. c.lubba15@imperial.ac.uk.ORCID http://orcid.org/0000-0003-0230-4035
Yann Le GuenDepartment of Bioengineering, Imperial College London, South Kensington, London, SW7 2AZ, UK.
Sarah JarvisDepartment of Bioengineering, Imperial College London, South Kensington, London, SW7 2AZ, UK.
Nick S JonesDepartment of Mathematics, Imperial College London, South Kensington, London, SW7 2AZ, UK.
Simon C CorkDepartment of Medicine, Imperial College London, South Kensington, London, SW7 2AZ, UK.
Amir EftekharDepartment of Electrical and Electronic Engineering, Imperial College London, South Kensington, London, SW7 2AZ, UK.
Simon R SchultzDepartment of Bioengineering, Imperial College London, South Kensington, London, SW7 2AZ, UK. s.schultz@imperial.ac.uk.

Funding

Engineering and Physical Sciences Research Council EP/L016737/1Engineering and Physical Sciences Research Council EP/N014529/1
6 · The paper itself

Abstract

Bioelectronic Medicines that modulate the activity patterns on peripheral nerves have promise as a new way of treating diverse medical conditions from epilepsy to rheumatism. Progress in the field builds upon time consuming and expensive experiments in living organisms. To reduce experimentation load and allow for a faster, more detailed analysis of peripheral nerve stimulation and recording, computational models incorporating experimental insights will be of great help. We present a peripheral nerve simulator that combines biophysical axon models and numerically solved and idealised extracellular space models in one environment. We modelled the extracellular space as a three-dimensional resistive continuum governed by the electro-quasistatic approximation of the Maxwell equations. Potential distributions were precomputed in finite element models for different media (homogeneous, nerve in saline, nerve in cuff) and imported into our simulator. Axons, on the other hand, were modelled more abstractly as one-dimensional chains of compartments. Unmyelinated fibres were based on the Hodgkin-Huxley model; for myelinated fibres, we adapted the model proposed by McIntyre et al. in 2002 to smaller diameters. To obtain realistic axon shapes, an iterative algorithm positioned fibres along the nerve with a variable tortuosity fit to imaged trajectories. We validated our model with data from the stimulated rat vagus nerve. Simulation results predicted that tortuosity alters recorded signal shapes and increases stimulation thresholds. The model we developed can easily be adapted to different nerves, and may be of use for Bioelectronic Medicine research in the future.

Indexed as

AlgorithmsComputer SimulationModels, NeurologicalAnimalsAxonsMalePeripheral NervesRatsRats, WistarBioelectronic medicinesBiophysicsFinite element modelPeripheral nerveSimulation

Identifiers

PMID29948844
PMCPMC6394768

What OpenQuestion holds

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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.