OSCR

The all-or-none repolarization in cardiac ventricular myocytes: an <i>in silico</i> characterization of a relevant biomarker of ventricular action potential.

Code ↔ Paper

The paper beside its authors' code: matches between them have not been computed for this paper yet.

Paper

Loaded from Europe PMC by your browser, not stored by OSCR: doi.org · Europe PMC

The paper is loaded when this pane is shown.

The authors' code

MATLAB · 163 lines · 3.4 KB · CC-BY-4.0

  1. % close all
  2. clear
  3. % clc
  4. % clf
  5. global T1
  6. global Amp2
  7. global dur2
  8. global CC_VC
  9. addpath C:\mystuff\work_2026\mfiles_Eugenio_currents\funzioni_modelli\
  10. addpath C:\mystuff\work_2026\mfiles_Eugenio_currents\IC
  11. addpath C:\mystuff\work_2026\mfiles_Eugenio_currents\bioms\
  12. % addpath C:\mystuff\work_2026\mfiles_eugenio_currents\restitution
  13. VC=zeros(1,131);
  14. % Der_media=zeros(1,131);
  15. for kk=1:80
  16. kk
  17. for qw=1:131
  18. T1=5+(kk-1)*5;
  19. dur2=100;
  20. % Amp2=67; % 82(10)
  21. if qw==31
  22. VClamp=0.1;
  23. else
  24. VClamp=31-qw;
  25. end
  26. VC(qw)=VClamp;
  27. nbeats = 1;
  28. t = [0, T1/1000]; % s
  29. font_size = 24;
  30. lin_wid = 1;
  31. %load('TorORd_IC.mat')
  32. load('Y_2000_INa_0')
  33. % Y0 = TorORd_CL_2000_ICaL_0_0;
  34. Y0=Y_2000_INa_0;
  35. % Y0=Y_2000;
  36. fcn = @model_Torord;
  37. V_idx = 1;
  38. Cai_idx = 6;
  39. V_scale = 1; % mV
  40. flag_ode = 1;
  41. scale = 1e3;
  42. t = t*scale;
  43. %% Run simulation
  44. %options = odeset('MaxStep', scale*1e-3, 'OutputFcn',@odewbar); %
  45. options = odeset('MaxStep', scale*1e-3); %
  46. [t_last, Y_last] = ode15s(@(x,y) fcn(x, y, flag_ode), t, Y0, options);
  47. Y0 = Y_last(size(Y_last,1),:);
  48. t1 = t_last;
  49. Vm1 = Y_last(:, V_idx)*V_scale;
  50. tvc=[t1(end),t1(end)+1];
  51. CC_VC=2;
  52. Y0(1)=VClamp;
  53. %options = odeset('MaxStep', scale*1e-3, 'OutputFcn',@odewbar); %
  54. options = odeset('MaxStep', scale*1e-3); %
  55. [t_last, Y_last] = ode15s(@(x,y) fcn(x, y, flag_ode), tvc, Y0, options);
  56. Y0 = Y_last(size(Y_last,1),:);
  57. t2 = t_last;
  58. Vm2 = Y_last(:, V_idx)*V_scale;
  59. tcc=[t2(end),t2(end)+500];
  60. CC_VC=1;
  61. %options = odeset('MaxStep', scale*1e-3, 'OutputFcn',@odewbar); %
  62. options = odeset('MaxStep', scale*1e-3); %
  63. [t_last, Y_last] = ode15s(@(x,y) fcn(x, y, flag_ode), tcc, Y0, options);
  64. Y0 = Y_last(size(Y_last,1),:);
  65. t3 = t_last;
  66. Vm3 = Y_last(:, V_idx)*V_scale;
  67. Vm=[Vm1;Vm2;Vm3];
  68. t=[t1;t2;t3];
  69. % [a,b]=min(abs(t3-(T1+100))); % seleziono sono i 100 ms dopo VC
  70. % derivata=diff(Vm3(1:b))./diff(t3(1:b));
  71. % Der_media(qw)=mean(derivata);
  72. t_deflections=t3(1):0.1:t3(end);
  73. Vm_deflections=interp1(t3,Vm3,t_deflections);
  74. [a,b]=find(t_deflections==t3(1)+100);
  75. Vm_defl(:,qw)=Vm_deflections(1:b);
  76. t_defl=t_deflections(1:b);
  77. end
  78. %% Extract and plot state variables on last beat
  79. % subplot(2,1,1)
  80. % plot(t, Vm, 'Linewidth', 1);hold on
  81. % xlabel('t (ms)'), ylabel('V_m (mV)')
  82. % xline(T1+100,':')
  83. % axis([0 400 -100 50])
  84. iniz_window=0;
  85. fin_window=100;
  86. [b,iniz]=min(abs(t_defl-(t_defl(1)+iniz_window)));
  87. [a,fin]=min(abs(t_defl-(t_defl(1)+fin_window)));
  88. T=t_defl(iniz:fin);
  89. V=Vm_defl(iniz:fin,:);
  90. derivata=diff(V)./diff(T');
  91. media_der=mean(derivata);
  92. VC=Vm_defl(1,:);
  93. Res(:,kk)=media_der';%%%%%%%%%%%%%%%%%%%%%%%%%%
  94. % subplot(2,1,2)
  95. % plot(VC,media_der);hold on
  96. %
  97. % ylim([-1 1.2])
  98. end
  99. TT=(1:1:kk)*5;
  100. surf(TT,VC,Res)
  101. Xq = TT(1):0.1:TT(end); Yq = VC(end):0.1:VC(1);
  102. [Xq,Yq] = meshgrid(Xq,Yq);
  103. Zq = interp2(TT,VC,Res,Xq,Yq,'spline');
  104. figure
  105. mesh(Xq,Yq,Zq);hold on
  106. view(0,90)
  107. axis([0 400 -100 40 -1 1])
  108. % cd C:\mystuff\work_2026\mfiles_eugenio_currents\restitution
  109. cd C:\mystuff\work_2026\data4
  110. load wf_2000
  111. plot(wf_2000(:,1),wf_2000(:,2),'w','LineWidth',2)
  112. axis([0 400 -100 40])
  113. colorbar
  114. xlabel('time (ms)')
  115. ylabel('Vm (mV)')
  116. cd C:\mystuff\work_2026\3d_surfaces
  117. save Y_2000_INa_0
  118. % cd C:\mystuff\work_2026\mfiles_eugenio_currents\restitution\3d_surfaces
  119. % save restit_1500

Torord_SRR_CC_VC_ITER_e_misura.m, under CC-BY-4.0 · at the source

Overview

Authors: Massimiliano Zaniboni1
  1. Department of Chemistry, Life Sciences and Environmental Sustainability, University of Parma, Parma, Italy
Institutions: University of Parma (Italy)
Journal: Frontiers in physiology, volume 17, article 1827577
Dates: received 10 March 2026; accepted 27 April 2026; published online 30 June 2026
Type: Research article · Language: English
License: CC BY
Identifiers: DOI 10.3389/fphys.2026.1827577 · PMID 42454072 · PMCID PMC13364564 · OpenAlex W7166760158
Open access: gold, a free copy (OpenAlex)
Status: code verified
Categories: computational modeling (no new data) (modality), human (organism), clinical / translational (subfield)
Keywords: all-or-none repolarization, biomarker of cardiac repolarization, cardiac action potential form, cardiac action potential repolarization, discontinuous conduction of cardiac action potential, gradients of repolarization
Topic: Cardiac electrophysiology and arrhythmias (Cardiology and Cardiovascular Medicine, Medicine), according to OpenAlex
Citations: not cited yet (Europe PMC); 32 references in the paper

Abstract

All-or-none repolarization (AONR) consists in the fact that brief hyperpolarizing current injections delivered during the early phase of the cardiac action potential (AP) can reach membrane potential values where small changes in the current can either lead the post-injection membrane potential to recover the previous AP waveform or suddenly repolarize to the resting state. The phenomenon, long known from the early studies on squid axon and Purkinje fibers, has been studied over the years. Here, by means of an updated human ventricular AP model, the form of AONR is described in detail, showing how it is modified by the pacing rate and by the changes in the ion channels active during the early phase of AP. A novel representation of AONR is proposed that makes it easier to appreciate the features of this phenomenon and its relationship with the corresponding AP. It is shown, for example, how the threshold for AONR changes in different models of human ventricular AP. The phenomenon is revisited by which different propensity to generate AONR in endocardial and epicardial cells can lead to transmural repolarization gradients and arrhythmias. It is also shown that the form of AONR is mostly independent from the corresponding AP waveform, as two almost identical AP waveforms show completely different thresholds for AONR. The main message of this study is that the threshold for AONR is an easily accessible feature of the AP, rich in information concerning AP dynamics, which should be taken into consideration as a fundamental electrophysiological biomarker in the process of fine-tuning human ventricular AP models.

Reproduced under the paper's license (CC BY), from the paper cited above.

Repository

Its files are read in the Code ↔ Paper reader above.

Zenodo 19666107

License: CC-BY-4.0
State: the link answers, verified on 27 September 2026
Evidence: files inventoried
Languages: MATLAB (1)
Size: 1 file, 1 script
Software Heritage: not checked
Found in: the text, “Conclusions”
Not found: README, license file, CITATION.cff, environment file, tests, continuous integration, documentation
Availability: 1 check, the latest on 27 September 2026: the link answers (HTTP 200)
  • 27 September 2026: the link answers (HTTP 200)
1 file

Tracing map

Proposed by the machine: these links were found in the paper and verified at the source, without human review. The map will receive a Zenodo DOI once one of the paper's authors has validated it with their ORCID.

What the map holds:

  • 1 repository of the authors' code, each at its verified commit, with its license and how the link was found in the paper;
  • 1 script, each with its path and the digest of its content;
  • no match between paragraphs and code yet;
  • neither the text of the paper nor the code itself.

Its JSON (tracing-map.json) is deposited on Zenodo with its DOI once the map is validated.

Data

No dataset and no data link were found in the paper.

Data availability statement

The raw data supporting the conclusions of this article will be made available by the authors, without undue reservation.

Reproduced under the paper's license (CC BY), from the paper cited above.

Versions

The history of this record: each version stored by the harvester or made by a correction of its authors or of the maintainers of its code, and what changed in its facts. The texts of the paper (its abstract, its availability statements) are not part of it; versions that changed only those are not listed.

Version 1, 27 September 2026: the first record

Recorded: type, language, journal, volume, pages, dates, 1 author, 6 keywords, 32 references.

Cite

This paper

Zaniboni, M. (2026). The all-or-none repolarization in cardiac ventricular myocytes: an <i>in silico</i> characterization of a relevant biomarker of ventricular action potential. Frontiers in physiology, 17, 1827577. https://doi.org/10.3389/fphys.2026.1827577

BibTeX

@article{zaniboni2026all,
author = {Zaniboni, Massimiliano},
title = {{The all-or-none repolarization in cardiac ventricular myocytes: an \<i\>in silico\</i\> characterization of a relevant biomarker of ventricular action potential}},
journal = {Frontiers in physiology},
year = {2026},
month = jun,
volume = {17},
pages = {1827577},
publisher = {Frontiers Media SA},
issn = {1664-042X},
doi = {10.3389/fphys.2026.1827577},
url = {https://doi.org/10.3389/fphys.2026.1827577},
pmid = {42454072},
pmcid = {PMC13364564}
}

RIS

TY - JOUR
AU - Zaniboni, Massimiliano
TI - The all-or-none repolarization in cardiac ventricular myocytes: an <i>in silico</i> characterization of a relevant biomarker of ventricular action potential
T2 - Frontiers in physiology
J2 - Front Physiol
PY - 2026
DA - 2026/06/30
VL - 17
SP - 1827577
SN - 1664-042X
PB - Frontiers Media SA
DO - 10.3389/fphys.2026.1827577
UR - https://doi.org/10.3389/fphys.2026.1827577
LA - en
ER -

CSL-JSON

{
"id": "10.3389/fphys.2026.1827577",
"type": "article-journal",
"title": "The all-or-none repolarization in cardiac ventricular myocytes: an <i>in silico</i> characterization of a relevant biomarker of ventricular action potential",
"container-title": "Frontiers in physiology",
"author": [
{
"family": "Zaniboni",
"given": "Massimiliano"
}
],
"container-title-short": "Front Physiol",
"volume": "17",
"page": "1827577",
"DOI": "10.3389/fphys.2026.1827577",
"PMID": "42454072",
"PMCID": "PMC13364564",
"ISSN": "1664-042X",
"publisher": "Frontiers Media SA",
"URL": "https://doi.org/10.3389/fphys.2026.1827577",
"language": "en",
"issued": {
"date-parts": [
[
2026,
6,
30
]
]
}
}

The tracing map gets a citation of its own once an author has validated it and it has a DOI.

Similar papers

The papers with a page that share the most with this one: the tools found in their code, their categories, datasets, cited references and authors, the rarest counting most.

[1] doi:10.1371/journal.pcbi.1014555 [code]
Body surface potential driven personalisation of electrophysiological digital twins in hypertrophic cardiomyopathy.
Journal: PLoS computational biology
In common: 1 reference
[2] doi:10.1038/s41540-026-00730-2 [code]
Sometimes extracellular recordings fail for good reasons.
Journal: NPJ systems biology and applications
In common: 1 reference
[3] doi:10.1523/jneurosci.1540-25.2026 [code]
Dendritic Inhibition Terminates Plateau Potentials in CA1 Pyramidal Neurons.
Journal: The Journal of neuroscience : the official journal of the Society for Neuroscience
In common: 1 reference
[4] doi:10.1038/s43856-026-01695-3 [code]
Predict neuromuscular performance in human epidural electrical stimulation: phase 1 trial interim results.
Journal: Communications medicine
In common: computational modeling (no new data), clinical / translational
[5] doi:10.1371/journal.pcbi.1014752 [code]
Hierarchical feature binding in a spiking neural network model of the primate ventral visual pathway.
Journal: PLoS computational biology
In common: computational modeling (no new data)
[6] doi:10.1371/journal.pcbi.1014701 [code]
Computer models predict differential dendritic vulnerability with ischemia and spreading depression.
Journal: PLoS computational biology
In common: computational modeling (no new data)
[7] doi:10.1126/sciadv.aef2894 [code]
Human cortical networks trade communication efficiency for computational reliability.
Journal: Science advances
In common: computational modeling (no new data)
[8] doi:10.1371/journal.pcbi.1014730 [code]
A unified model of short- and long-term plasticity: Effects on network connectivity and information capacity.
Journal: PLoS computational biology
In common: computational modeling (no new data)
[9] doi:10.1021/acs.jcim.6c01299 [code]
Targeting BCL-2 through Deep Learning-Based Drug Repurposing: A Multimodal Approach Combining Diffusion-Based Generative Modeling, Neural Relational Inference, and In Vitro Validation.
Journal: Journal of chemical information and modeling
In common: computational modeling (no new data)
[10] doi:10.1073/pnas.2616911123 [code]
Cerebellar microcircuits enable robust evidence-based decisions through cortico-cerebellar coupling.
Journal: Proceedings of the National Academy of Sciences of the United States of America
In common: computational modeling (no new data)

Contribute

The authors of this paper can claim it, correct its record and validate its tracing map, and the maintainers of its code (its owner, or a public member of its organization) correct what it says of their repository; anyone signed in can ask for its removal. Every request goes to OSCR's own machine, which answers it; your account page follows them.

Sign in with ORCID to claim this paper as one of its authors, correct its record or validate its tracing map: when the paper's metadata lists your ORCID iD, you are recognized at once. Maintainers of its code: sign in with GitHub, then claim the repository on your account page.

Request its removal

To ask OSCR to remove this record, the copies of its authors' scripts or its tracing map, use the removal request page: signed in, you say who you are, what to remove and why, then review and confirm the request. Published rules decide every request (how).

Discussion, reproductions, activity

Discussion: questions and error reports about this paper and its code, from signed-in readers and its authors. It opens with sign-in.

Reproductions: reports from readers who ran the authors' code: what they reproduced, with which environment, commit and data. It opens with sign-in.

Activity: what happens around this paper: new versions of its record, its map's validation, discussions and reproductions. It opens with sign-in.