Evidence map›Paper›PMID 24853751›Full record

ArticleBiophysical journal2014

Voltage and calcium dynamics both underlie cellular alternans in cardiac myocytes.

Willemijn Groenendaal, Francis A Ortega, Trine Krogh-Madsen, David J Christini

Abstract read
In one paragraph

Article in Biophysical journal, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing 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

18 citing papers in PubMed.

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  15. From channels to systems: CaThe Journal of physiology · 2017
    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

4 authors.

Willemijn GroenendaalGreenberg Division of Cardiology, Weill Cornell Medical College, New York, New York.
Francis A OrtegaGreenberg Division of Cardiology, Weill Cornell Medical College, New York, New York; Department of Physiology and Biophysics, Weill Cornell Medical College, New York, New York.
Trine Krogh-MadsenGreenberg Division of Cardiology, Weill Cornell Medical College, New York, New York; Institute for Computational Biomedicine, Weill Cornell Medical College, New York, New York.
David J ChristiniGreenberg Division of Cardiology, Weill Cornell Medical College, New York, New York; Institute for Computational Biomedicine, Weill Cornell Medical College, New York, New York; Department of Physiology and Biophysics, Weill Cornell Medical College, New York, New York. Electronic address: dchristi@med.cornell.edu.

Funding

Real-time control system for biological experimentsR01EB016407 · NIBIB · WEILL MEDICAL COLL OF CORNELL UNIV · PI CHRISTINI, DAVID J. · 2013 to 2016
$2.7M
Mechanisms of Cardiac AlternansR01HL094620 · NHLBI · WEILL MEDICAL COLL OF CORNELL UNIV · PI CHRISTINI, DAVID J. · 2009 to 2013
$1.9M
NHLBI NIH HHS R01 HL094620NHLBI NIH HHS R01HL094620NIBIB NIH HHS R01 EB016407NIBIB NIH HHS R01EB016407
6 · The paper itself

Abstract

Cardiac alternans, a putative trigger event for cardiac reentry, is a beat-to-beat alternation in membrane potential and calcium transient. Alternans was originally attributed to instabilities in transmembrane ion channel dynamics (i.e., the voltage mechanism). As of this writing, the predominant view is that instabilities in subcellular calcium handling are the main underlying mechanism. That being said, because the voltage and calcium systems are bidirectionally coupled, theoretical studies have suggested that both mechanisms can contribute. To date, to our knowledge, no experimental evidence of such a dual role within the same cell has been reported. Here, a combined electrophysiological and calcium imaging approach was developed and used to illuminate the contributions of voltage and calcium dynamics to alternans. An experimentally feasible protocol, quantification of subcellular calcium alternans and restitution slope during cycle-length ramping alternans control, was designed and validated. This approach allows simultaneous illumination of the contributions of voltage and calcium-driven instability to total cellular instability as a function of cycle-length. Application of this protocol in in vitro guinea-pig left-ventricular myocytes demonstrated that both voltage- and calcium-driven instabilities underlie alternans, and that the relative contributions of the two systems change as a function of pacing rate.

Indexed as

Electrophysiological PhenomenaAnimalsCalciumGlucansGuinea PigsModels, BiologicalMolecular ImagingMyocytes, CardiacalternanCalciumGlucans

Identifiers

PMID24853751
PMCPMC4052344

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.