Evidence map›Paper›PMID 40560823›Full record

ArticleThe Journal of physiology2026

An integrated platform for 2-D and 3-D optical and electrical mapping of arrhythmias in Langendorff-perfused rabbit hearts.

Jimena Siles, Vinícius Silva, Tainan Neves, Italo Sandoval, Angélica Quadros, Giovanni Weber, Óscar Barquero, Ilija Uzelac, João Salinet

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 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
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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

9 authors.

Jimena SilesHEartLab, Federal University of ABC, São Paulo, Brazil.ORCID https://orcid.org/0000-0001-7213-9149
Vinícius SilvaHEartLab, Federal University of ABC, São Paulo, Brazil.
Tainan NevesHEartLab, Federal University of ABC, São Paulo, Brazil.ORCID https://orcid.org/0000-0002-9331-6690
Italo SandovalHEartLab, Federal University of ABC, São Paulo, Brazil.
Angélica QuadrosHEartLab, Federal University of ABC, São Paulo, Brazil.ORCID https://orcid.org/0009-0004-2080-7351
Giovanni WeberHEartLab, Federal University of ABC, São Paulo, Brazil.
Óscar BarqueroRey Juan Carlos University, Fuenlabrada, Madrid, Spain.
Ilija UzelacVirginia Commonwealth University, School of Medicine, VA, USA.
João SalinetHEartLab, Federal University of ABC, São Paulo, Brazil.ORCID https://orcid.org/0000-0003-2906-9397

Funding

CNPq INCT INTERAS 406761/2022-1São Paulo Research Foundation (FAPESP) 2018/25606-2São Paulo Research Foundation (FAPESP) 2020/03601-9São Paulo Research Foundation (FAPESP) 2023/06306-6São Paulo Research Foundation (FAPESP) 2024/02521-2
6 · The paper itself

Abstract

Electrophysiological mapping is essential for understanding these mechanisms and guiding therapeutic treatments. However, approaches such as invasive electrical mapping, body surface mapping and electrocardiographic imaging face challenges, including low spatial resolution, far-field interference and signal processing limitations. By contrast, panoramic optical mapping, using fluorescent dyes, offers high spatial resolution and allows direct measurement of cellular action potential ex situ. Can the integration of panoramic optical mapping with electrical mapping overcome the limitations of the above-cited techniques and provide deeper insights into arrhythmic mechanisms? To investigate this, we developed an experimental setup that combines 3-D panoramic optical mapping with multi-electrode epicardial electrical mapping and non-invasive electrical mapping (torso-tank setup) for electrocardiographic imaging in Langendorff-perfused rabbit hearts. Our results confirm the feasibility of using simultaneous optical and electrical mapping under sinus rhythm, as well as in atrial and ventricular arrhythmias, using time, frequency and phase analyses. During sinus rhythm and ventricular tachycardia, wavefront propagation showed concordance between modalities, where diverges are observed for atrial arrhythmias. Dominant frequency analysis could recover the frequency of activation better than the inverse of cycle length, and outcomes from all mapping modalities agreed. Reconstructed electrograms presented a good similarity compared to electrograms. By correlating optical and electrical mapping, clinically relevant arrhythmia markers and targets for ablation, from invasive and non-invasive mapping can be better understood and localised. This platform could also serve as a test bed for studying drug effects, connecting changes from cellular action potential levels to whole-heart electrophysiology. KEY POINTS: Cardiac arrhythmias are still a significant challenge in electrophysiology, with advancements in experimental and clinical research improving our understanding of mechanisms and target for ablation. Current electrical mapping technology, both invasive and non-invasive, is used in science and by commercial systems to identify arrhythmic episodes and mechanisms, but has several limitations mimicking the true electrophysiology behaviour. Optical mapping uses fluorescent dyes to measure transmembrane action potentials with high spatial resolution. When combined with electrical mapping, it can enhance cardiac arrhythmia studies and mapping technologies. A novel 3-D platform that integrates panoramic and electrical mapping techniques (epicardium, non-invasive torso-tank and electrocardiographic imaging) is presented and validated in isolated rabbit hearts, highlighting that the mapping strategies do not always agree, helping to further improve commercial systems.

Indexed as

Arrhythmias, CardiacElectrophysiologic Techniques, CardiacHeartAction PotentialsAnimalsElectrocardiographyEpicardial MappingIsolated Heart PreparationMalePerfusionRabbitsVoltage-Sensitive Dye Imagingaccurate diagnosiscardiac mappingelectrical mappingelectrocardiographic imagingpanoramic optical mappingtorso‐tank setup

Identifiers

PMID40560823
PMCPMC13327769

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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.