Evidence map›Paper›PMID 28038425›Full record

ArticleRedox biology2017

Knock out of the NADPH oxidase Nox4 has no impact on life span in mice.

Flavia Rezende, Christoph Schürmann, Susanne Schütz, Sabine Harenkamp, Eva Herrmann, Michael Seimetz, Norbert Weißmann, Katrin Schröder

Open access · goldAbstract read
In one paragraph

Article in Redox biology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing 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

15 citing papers in PubMed, 27 citations in OpenAlex.

  1. Trial
  2. Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. NOX Inhibitors: From Bench to Naxibs to Bedside.Handbook of experimental pharmacology · 2021
    Article
  8. Review
  9. NoxO1 Knockout Promotes Longevity in Mice.Antioxidants (Basel, Switzerland) · 2020
    Article
  10. Article
  11. Article
  12. Review
  13. Review
  14. Hypoxia enhances HRedox biology · 2018
    Article
  15. 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

8 authors at 2 institutions in 1 country.

Flavia RezendeInstitute for Cardiovascular Physiology, Goethe-University, Frankfurt, Germany.
Christoph SchürmannInstitute for Cardiovascular Physiology, Goethe-University, Frankfurt, Germany.
Susanne SchützInstitute for Cardiovascular Physiology, Goethe-University, Frankfurt, Germany.
Sabine HarenkampInstitute for Cardiovascular Physiology, Goethe-University, Frankfurt, Germany.
Eva HerrmannInstituts für Biostatistik und Mathematische Modellierung, Goethe-University, Frankfurt, Germany.
Michael SeimetzJustus-Liebig University, Giessen, German Center for Lung Research (DZL), Germany; Excellence Cluster Cardiovascular and Pulmonary System (ECCPS), Germany.
Norbert WeißmannJustus-Liebig University, Giessen, German Center for Lung Research (DZL), Germany; Excellence Cluster Cardiovascular and Pulmonary System (ECCPS), Germany.
Katrin SchröderInstitute for Cardiovascular Physiology, Goethe-University, Frankfurt, Germany; Excellence Cluster Cardiovascular and Pulmonary System (ECCPS), Germany; German Center for Cardiovascular Research (DZHK), Partner site RheinMain, Frankfurt, Germany. Electronic address: Schroeder@vrc.uni-frankfurt.de.
Goethe University Frankfurt · DEGerman Center for Lung Research · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The free radical theory of aging suggests reactive oxygen species as a main reason for accumulation of damage events eventually leading to aging. Nox4, a member of the family of NADPH oxidases constitutively produces ROS and therefore has the potential to be a main driver of aging. Herein we analyzed the life span of Nox4 deficient mice and found no difference when compared to their wildtype littermates. Accordingly neither Tert expression nor telomere length was different in cells isolated from those animals. In fact, Nox4 mRNA expression in lungs of wildtype mice dropped with age. We conclude that Nox4 has no influence on lifespan of healthy mice.

Indexed as

AnimalsEpithelial CellsFemaleGene ExpressionLongevityLungMaleMiceMice, Inbred C57BLMice, KnockoutNADPH Oxidase 4Primary Cell CultureTelomeraseTelomere HomeostasisNADPH Oxidase 4Nox4 protein, mouseTelomeraseTert protein, mouseAgingNox4

Identifiers

PMID28038425
PMCPMC5196091
OpenAlexW2561992980

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.