Evidence map›Paper›PMID 29222390›Full record

ArticleJournal of the American Heart Association2017

Sodium Channel Remodeling in Subcellular Microdomains of Murine Failing Cardiomyocytes.

Mathilde R Rivaud, Esperanza Agullo-Pascual, Xianming Lin, Alejandra Leo-Macias, Mingliang Zhang, Eli Rothenberg, Connie R Bezzina, Mario Delmar, Carol Ann Remme

Open access · goldAbstract read
In one paragraph

Article in Journal of the American Heart Association, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
2.7field-weighted citation impact, top 8% of its field
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

34 citing papers in PubMed, 45 citations in OpenAlex.

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  15. Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2023
    Review
  16. Article
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  18. Article
  19. Review
  20. Scanning Ion Conductance Microscopy.Chemical reviews · 2021
    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

9 authors at 4 institutions in 2 countries.

Mathilde R RivaudHeart Center, Department of Clinical and Experimental Cardiology, Academic Medical Center, University of Amsterdam, the Netherlands.
Esperanza Agullo-PascualDivision of Cardiology, New York University Medical Center, New York, NY.
Xianming LinDivision of Cardiology, New York University Medical Center, New York, NY.
Alejandra Leo-MaciasDivision of Cardiology, New York University Medical Center, New York, NY.
Mingliang ZhangDivision of Cardiology, New York University Medical Center, New York, NY.
Eli RothenbergDepartment of Biochemistry and Molecular Pharmacology, NYU-School of Medicine, New York, NY.
Connie R BezzinaHeart Center, Department of Clinical and Experimental Cardiology, Academic Medical Center, University of Amsterdam, the Netherlands.
Mario DelmarDivision of Cardiology, New York University Medical Center, New York, NY c.a.remme@amc.uva.nl mario.delmar@nyumc.org.
Carol Ann RemmeHeart Center, Department of Clinical and Experimental Cardiology, Academic Medical Center, University of Amsterdam, the Netherlands c.a.remme@amc.uva.nl mario.delmar@nyumc.org.
New York University · USColumbia University Irving Medical Center · USUniversity of Amsterdam · NLAcademic Medical Center · NL

Funding

PH REGULATION OF CONNEXIN43--INTERMEDIARY STEPSR01GM057691 · NIGMS · UPSTATE MEDICAL UNIVERSITY · PI DELMAR, MARIO · 1999 to 2016
$5.6M
Role of PKP2 in epicardial structure and functionR01HL136179 · NHLBI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI DELMAR, MARIO, MORLEY, GREGORY E · 2017 to 2020
$3.1M
Role of desmosomes in cardiac electrical functionR01HL134328 · NHLBI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI DELMAR, MARIO, MORLEY, GREGORY E · 2016 to 2019
$2.6M
NHLBI NIH HHS R01 HL134328NHLBI NIH HHS R01 HL136179NIGMS NIH HHS R01 GM057691
6 · The paper itself

Abstract

backgroundCardiac sodium channel (NaV1.5) dysfunction contributes to arrhythmogenesis during pathophysiological conditions. Nav1.5 localizes to distinct subcellular microdomains within the cardiomyocyte, where it associates with region-specific proteins, yielding complexes whose function is location specific. We herein investigated sodium channel remodeling within distinct cardiomyocyte microdomains during heart failure. METHODS AND

resultsMice were subjected to 6 weeks of transverse aortic constriction (TAC; n=32) to induce heart failure. Sham-operated on mice were used as controls (n=20). TAC led to reduced left ventricular ejection fraction, QRS prolongation, increased heart mass, and upregulation of prohypertrophic genes. Whole-cell sodium current (I

conclusionsHeart failure induces structural remodeling of the intercalated disc, LM, and microtubule network in cardiomyocytes. These adaptations are accompanied by alterations in Na

Indexed as

AnimalsDisease Models, AnimalHeart FailureMaleMiceMice, Inbred C57BLMyocytes, CardiacNAV1.5 Voltage-Gated Sodium ChannelPatch-Clamp TechniquesSubcellular FractionsNAV1.5 Voltage-Gated Sodium Channelheart failureimagingmicrodomainsmicroscopyNa+ currentpatch‐clampsodium channelssubcellular

Identifiers

PMID29222390
PMCPMC5779058
OpenAlexW2774485847

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

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.