Evidence map›Paper›PMID 29288034›Full record

ArticleHeart rhythm2018

Structural and functional remodeling of the atrioventricular node with aging in rats: The role of hyperpolarization-activated cyclic nucleotide-gated and ryanodine 2 channels.

Yawer Saeed, Ian P Temple, Zoltan Borbas, Andrew Atkinson, Joseph Yanni, Michal Maczewski, Urszula Mackiewicz, Mariam Aly, Sunil Jit R J Logantha, Clifford J Garratt and 1 more

Open access · hybridAbstract read
In one paragraph

Article in Heart rhythm, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.6field-weighted citation impact, top 14% 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

16 citing papers in PubMed, 39 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Genetic background determines the severity of age-dependent cardiac structural abnormalities and arrhythmia susceptibility in Scn5a-1798insD mice.Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology · 2024
    Article
  5. The Senescent Heart-"Age Doth Wither Its Infinite Variety".International journal of molecular sciences · 2024
    Review
  6. The Dysfunction of CaInternational journal of molecular sciences · 2023
    Review
  7. Article
  8. Article
  9. CPVT and Complete Atrio-Ventricular Block: The Flipside of the Same Coin.Journal of cardiovascular development and disease · 2023
    Article
  10. Review: HCN Channels in the Heart.Current cardiology reviews · 2022
    Review
  11. RyR2 and Calcium Release in Heart Failure.Frontiers in physiology · 2021
    Review
  12. Cardiac and neuronal HCN channelopathies.Pflugers Archiv : European journal of physiology · 2020
    Review
  13. Review
  14. Review
  15. Article
  16. 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

11 authors at 2 institutions in 2 countries.

Yawer SaeedInstitute of Cardiovascular Sciences, University of Manchester, Manchester, United Kingdom; Manchester Heart Centre, Central Manchester University Hospitals NHS Trust, Manchester, United Kingdom.
Ian P TempleInstitute of Cardiovascular Sciences, University of Manchester, Manchester, United Kingdom.
Zoltan BorbasInstitute of Cardiovascular Sciences, University of Manchester, Manchester, United Kingdom; Manchester Heart Centre, Central Manchester University Hospitals NHS Trust, Manchester, United Kingdom.
Andrew AtkinsonInstitute of Cardiovascular Sciences, University of Manchester, Manchester, United Kingdom.
Joseph YanniInstitute of Cardiovascular Sciences, University of Manchester, Manchester, United Kingdom.
Michal MaczewskiDepartment of Clinical Physiology, Centre of Postgraduate Medical Education, Warsaw, Poland.
Urszula MackiewiczDepartment of Clinical Physiology, Centre of Postgraduate Medical Education, Warsaw, Poland.
Mariam AlyInstitute of Cardiovascular Sciences, University of Manchester, Manchester, United Kingdom.
Sunil Jit R J LoganthaInstitute of Cardiovascular Sciences, University of Manchester, Manchester, United Kingdom.
Clifford J GarrattInstitute of Cardiovascular Sciences, University of Manchester, Manchester, United Kingdom; Manchester Heart Centre, Central Manchester University Hospitals NHS Trust, Manchester, United Kingdom.
Halina DobrzynskiInstitute of Cardiovascular Sciences, University of Manchester, Manchester, United Kingdom. Electronic address: halina.dobrzynski@manchester.ac.uk.
University of Manchester · GBPostgraduate School of Molecular Medicine · PL

Funding

British Heart Foundation RG/11/18/29257British Heart Foundation RG/18/2/33392
6 · The paper itself

Abstract

backgroundAging is associated with an increased incidence of atrioventricular nodal (AVN) dysfunction.

objectiveThe aim of this study was to investigate the structural and functional remodeling in the atrioventricular junction (AVJ) with aging.

methodsElectrophysiology, histology, and immunohistochemistry experiments on male Wistar Hannover rats aged 3 months (n = 24) and 2 years (n = 15) were performed. Atrio-His (AH) interval, Wenkebach cycle length (WBCL), and AVN effective refractory period (AVNERP) were measured. Cesium (2 mM) was used to block hyperpolarization-activated cyclic nucleotide-gated (HCN) channels, while ryanodine (2 μM) was used to block ryanodine 2 (RyR2) channels. Protein expression from different regions of the AVJ was studied using immunofluorescence. The expression of connexins (connexin 43 and connexin 40), ion channels (Hyperpolarization-activated cyclic nucleotide-gated channel 4 (HCN4), voltage sensitive sodium channel (Na

resultsWithout drugs to block HCN and RyR2 channels, there was prolongation of the AH interval, WBCL, and AVNERP (P < .05) with aging. In young rats only, cesium prolonged the AH interval, WBCL, and AVNERP (P < .01). Ryanodine prolonged the AH interval and WBCL (P < .01) in both young and old rats. Immunofluorescence revealed that with aging, connexin 43, HCN4, Na

conclusionHeterogeneous ion channel expression changes were observed in the AVJ with aging. For the first time, we have shown that HCN and RyR2 play an important role in AVN dysfunction with aging.

Indexed as

AgingAnimalsAtrioventricular NodeHyperpolarization-Activated Cyclic Nucleotide-Gated ChannelsImmunohistochemistryMaleModels, AnimalPatch-Clamp TechniquesRatsRats, WistarRyanodineRyanodine Receptor Calcium Release ChannelHyperpolarization-Activated Cyclic Nucleotide-Gated ChannelsRyanodineRyanodine Receptor Calcium Release ChannelAgingAV nodeI(f)Ion channel expressionRyanodine

Identifiers

PMID29288034
PMCPMC5934612
OpenAlexW2776276258

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.