Evidence map›Paper›PMID 31417144›Full record

ArticleScientific reports2019

Novel method for action potential measurements from intact cardiac monolayers with multiwell microelectrode array technology.

Heather B Hayes, Anthony M Nicolini, Colin A Arrowood, Stacie A Chvatal, David W Wolfson, Hee Cheol Cho, Denise D Sullivan, Jérome Chal, Bernard Fermini, Mike Clements and 2 more

Abstract read
In one paragraph

Article in Scientific reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers.

0numbers the graph read from it
0cells of the map it votes in
47citing 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

47 citing papers in PubMed.

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  15. hiPSC-CM electrophysiology: impact of temporal changes and study parameters on experimental reproducibility.American journal of physiology. Heart and circulatory physiology · 2024
    Article
  16. Article
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  18. Review
  19. Anthracycline Toxicity: Light at the End of the Tunnel?Annual review of pharmacology and toxicology · 2024
    Review
  20. Review
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

12 authors.

Heather B HayesAxion Biosystems, Inc, Atlanta, GA, USA.
Anthony M NicoliniAxion Biosystems, Inc, Atlanta, GA, USA.
Colin A ArrowoodAxion Biosystems, Inc, Atlanta, GA, USA.
Stacie A ChvatalAxion Biosystems, Inc, Atlanta, GA, USA.
David W WolfsonEmory University, Atlanta, GA, USA.ORCID http://orcid.org/0000-0003-3850-3925
Hee Cheol ChoEmory University, Atlanta, GA, USA.
Denise D SullivanAxion Biosystems, Inc, Atlanta, GA, USA.
Jérome ChalCoyne Scientific, Atlanta, GA, USA.
Bernard FerminiCoyne Scientific, Atlanta, GA, USA.
Mike ClementsAxion Biosystems, Inc, Atlanta, GA, USA.
James D RossAxion Biosystems, Inc, Atlanta, GA, USA.
Daniel C MillardAxion Biosystems, Inc, Atlanta, GA, USA. dmillard@axion-biosystems.com.

Funding

Patterning myocardial specification of human pluripotent stem cellsR01HL143065 · NHLBI · JOHNS HOPKINS UNIVERSITY · PI CHO, HEE CHEOL · 2019 to 2022
$2.3M
Molecular determinants of the cardiac pacemaker automaticityR01HL111646 · NHLBI · EMORY UNIVERSITY · PI CHO, HEE CHEOL · 2012 to 2016
$2.0M
NHLBI NIH HHS R01 HL111646NHLBI NIH HHS R01 HL143065
6 · The paper itself

Abstract

The cardiac action potential (AP) is vital for understanding healthy and diseased cardiac biology and drug safety testing. However, techniques for high throughput cardiac AP measurements have been limited. Here, we introduce a novel technique for reliably increasing the coupling of cardiomyocyte syncytium to planar multiwell microelectrode arrays, resulting in a stable, label-free local extracellular action potential (LEAP). We characterized the reliability and stability of LEAP, its relationship to the field potential, and its efficacy for quantifying AP morphology of human induced pluripotent stem cell derived and primary rodent cardiomyocytes. Rise time, action potential duration, beat period, and triangulation were used to quantify compound responses and AP morphology changes induced by genetic modification. LEAP is the first high throughput, non-invasive, label-free, stable method to capture AP morphology from an intact cardiomyocyte syncytium. LEAP can accelerate our understanding of stem cell models, while improving the automation and accuracy of drug testing.

Indexed as

MicroelectrodesAction PotentialsAnimalsAnimals, NewbornElectroporationHeartHumansInduced Pluripotent Stem CellsIon ChannelsMyocytes, CardiacRatsSignal Processing, Computer-AssistedTime FactorsIon Channels

Identifiers

PMID31417144
PMCPMC6695445

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.