Evidence map›Paper›PMID 17286959›Full record

ArticleBiochemical and biophysical research communications2007

Expression of skeletal muscle Na(V)1.4 Na channel isoform in canine cardiac Purkinje myocytes.

Yongxia Qu, Eddy Karnabi, Mohamed Chahine, Mario Vassalle, Mohamed Boutjdir

Open access · greenAbstract read
In one paragraph

Article in Biochemical and biophysical research communications, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
0.7field-weighted citation impact, top 31% 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

12 citing papers in PubMed, 14 citations in OpenAlex.

  1. C-Terminus of CaCells · 2026
    Article
  2. Reduced NaAmerican journal of physiology. Heart and circulatory physiology · 2020
    Article
  3. Review
  4. Article
  5. Voltage-gated sodium channels in the mammalian heart.Global cardiology science & practice · 2014
    Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Silencing of Cav1.2 gene in neonatal cardiomyocytes by lentiviral delivered shRNA.Biochemical and biophysical research communications · 2009
    Article
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

5 authors at 3 institutions in 2 countries.

Yongxia QuVA New York Harbor Healthcare System, Brooklyn, NY 11209, USA.
Eddy Karnabi
Mohamed Chahine
Mario Vassalle
Mohamed Boutjdir
SUNY Downstate Health Sciences University · USNew York University · USUniversité Laval · CA

Funding

Role of Ca channels in congenital heart blockR01HL077494 · NHLBI · NARROWS INSTITUTE FOR BIOMEDICAL RES INC · PI BOUTJDIR, MOHAMED · 2004 to 2007
$1.2M
NHLBI NIH HHS R01 HL-077494NHLBI NIH HHS R01 HL077494NHLBI NIH HHS R01 HL077494-01NHLBI NIH HHS R01 HL077494-02NHLBI NIH HHS R01 HL077494-03
6 · The paper itself

Abstract

BACKGROUND AND

aimThe action potential plateau of Purkinje fibers is particularly sensitive to tetrodotoxin (TTX) and this could be due to a TXX-sensitive Na(+) current. The expression of TTX-sensitive neuronal Na(V)1.1 and Na(V)1.2 isoforms has been reported in canine Purkinje myocytes. Our aim was to investigate by means of biochemical and functional techniques whether the TTX-sensitive skeletal Na(V)1.4 isoform is also expressed in canine cardiac Purkinje myocytes. METHODS AND

resultsUsing Na(V)1.4 specific primers, a PCR product corresponding to Na(V)1.4 was amplified from canine Purkinje fibers RNA and confirmed by sequencing and megablast of the gene bank. Confocal indirect immunostaining using anti-Na(V)1.4 antibody demonstrates distinct sarcolemmal staining pattern compared to that of the cardiac isoform Na(V)1.5. Expression of Na(V)1.4 in tsA201 cells yielded a TTX-sensitive Na(+) current with an IC(50) of 10nM.

conclusionsThese results demonstrate the expression of the TTX-sensitive Na(V)1.4 channel in canine cardiac Purkinje myocytes. This novel finding suggests a role of Na(V)1.4 channel in Purkinje myocytes and thus has important clinical implications for the mechanisms and management of ventricular arrhythmias originating in the Purkinje network.

Indexed as

Action PotentialsAnimalsBase SequenceDNA PrimersDogsGene Expression RegulationHeartMuscle CellsMuscle ProteinsMuscle, SkeletalPurkinje FibersRecombinant ProteinsReverse Transcriptase Polymerase Chain ReactionRNA, MessengerSodium ChannelsTetrodotoxinDNA PrimersMuscle ProteinsRecombinant ProteinsRNA, MessengerSodium ChannelsTetrodotoxin

Identifiers

PMID17286959
PMCPMC1849952
OpenAlexW2125220201

What OpenQuestion holds

Textmetadata
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.