Evidence map›Paper›PMID 26989455›Full record

ArticleOxidative medicine and cellular longevity2016

Age-Dependent Demethylation of Sod2 Promoter in the Mouse Femoral Artery.

Albert Nguyen, François Leblond, Maya Mamarbachi, Steve Geoffroy, Eric Thorin

Open access · hybridAbstract read
In one paragraph

Article in Oxidative medicine and cellular longevity, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

11 citing papers in PubMed, 14 citations in OpenAlex.

  1. Microvascular Health as a Key Determinant of Organismal Aging.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Review
  2. Article
  3. Review
  4. DNA Methylation Aberrant in Atherosclerosis.Frontiers in pharmacology · 2022
    Review
  5. Targeting Epigenetic Mechanisms in Vascular Aging.Frontiers in cardiovascular medicine · 2021
    Review
  6. Article
  7. Review
  8. Extracellular Spermine Activates DNA Methyltransferase 3A and 3B.International journal of molecular sciences · 2019
    Article
  9. Review
  10. Mechanisms of Vascular Aging.Circulation research · 2018
    Review
  11. 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 2 institutions in 1 country.

Albert NguyenDepartment of Pharmacology, Faculty of Medicine, Université de Montréal, Montreal, QC, Canada H3T 1J4; Research Centre, Montreal Heart Institute, 5000 Belanger Street, Montreal, QC, Canada H1T 1C8.
François LeblondDepartment of Pharmacology, Faculty of Medicine, Université de Montréal, Montreal, QC, Canada H3T 1J4; Research Centre, Montreal Heart Institute, 5000 Belanger Street, Montreal, QC, Canada H1T 1C8; Novartis Pharmaceuticals Canada Inc., Dorval, QC, Canada H9S 1A9.
Maya MamarbachiResearch Centre, Montreal Heart Institute, 5000 Belanger Street, Montreal, QC, Canada H1T 1C8.
Steve GeoffroyResearch Centre, Montreal Heart Institute, 5000 Belanger Street, Montreal, QC, Canada H1T 1C8.
Eric ThorinResearch Centre, Montreal Heart Institute, 5000 Belanger Street, Montreal, QC, Canada H1T 1C8; Department of Surgery, Faculty of Medicine, Université de Montréal, Montreal, QC, Canada H3T 1J4.
Montreal Heart Institute · CAUniversité de Montréal · CA

Funding

Canadian Institutes of Health Research MOP 14496
6 · The paper itself

Abstract

We studied the age-dependent regulation of the expression of the antioxidant enzyme manganese superoxide dismutase (MnSOD encoded by Sod2) through promoter methylation. C57Bl/6 mice were either (i) sedentary (SED), (ii) treated with the antioxidant catechin (CAT), or (iii) voluntarily exercised (EX) from weaning (1-month old; mo) to 9 mo. Then, all mice aged sedentarily and were untreated until 12 mo. Sod2 promoter methylation was similar in all groups in 9 mo but decreased (p < 0.05) in 12 mo SED mice only, which was associated with an increased (p < 0.05) transcriptional activity in vitro. At all ages, femoral artery endothelial function was maintained; this was due to an increased (p < 0.05) contribution of eNOS-derived NO in 12 mo SED mice only. CAT and EX prevented these changes in age-related endothelial function. Thus, a ROS-dependent epigenetic positive regulation of Sod2 gene expression likely represents a defense mechanism prolonging eNOS function in aging mouse femoral arteries.

Indexed as

DNA MethylationPromoter Regions, GeneticTranscription, GeneticAgingAnimalsCatechinFemoral ArteryMiceNitric OxideNitric Oxide Synthase Type IIIPhysical Conditioning, AnimalSuperoxide DismutaseSuperoxide Dismutase 2CatechinNitric OxideNitric Oxide Synthase Type IIINos3 protein, mouseSuperoxide DismutaseSuperoxide Dismutase 2

Identifiers

PMID26989455
PMCPMC4771915
OpenAlexW2273979249

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.