Evidence map›Paper›PMID 26230326›Full record

ArticlePloS one2015

The Effects of Xanthine Oxidoreductase Inhibitors on Oxidative Stress Markers following Global Brain Ischemia Reperfusion Injury in C57BL/6 Mice.

Masahiro Yamaguchi, Ken Okamoto, Teruo Kusano, Yoko Matsuda, Go Suzuki, Akira Fuse, Hiroyuki Yokota

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.9field-weighted citation impact, top 10% 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

14 citing papers in PubMed, 37 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Xanthine oxidase mediates chronic stress-induced cerebrovascular dysfunction and cognitive impairment.Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism · 2023
    Article
  6. Article
  7. Xanthine Oxidoreductase Inhibitors.Handbook of experimental pharmacology · 2021
    Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Review
  14. Xanthine oxidase inhibitors and sepsis.International journal of immunopathology and pharmacology
    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

7 authors at 2 institutions in 1 country.

Masahiro YamaguchiNippon Medical School, Emergency and Critical Care Medicine, Tokyo, Japan.
Ken OkamotoNippon Medical School, Biochemistry and Molecular Biology, Tokyo, Japan.
Teruo KusanoNippon Medical School, Biochemistry and Molecular Biology, Tokyo, Japan.
Yoko MatsudaTokyo Metropolitan Geriatric Hospital and Institute of Gerontology, Department of Pathology, Tokyo, Japan.
Go SuzukiNippon Medical School, Emergency and Critical Care Medicine, Tokyo, Japan.
Akira FuseNippon Medical School, Emergency and Critical Care Medicine, Tokyo, Japan.
Hiroyuki YokotaNippon Medical School, Emergency and Critical Care Medicine, Tokyo, Japan.
Nippon Medical School · JPTokyo Metropolitan Geriatric Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We demonstrated that 3-nitrotyrosine and 4-hydroxy-2-nonenal levels in mouse brain were elevated from 1 h until 8 h after global brain ischemia for 14 min induced with the 3-vessel occlusion model; this result indicates that ischemia reperfusion injury generated oxidative stress. Reactive oxygen species production was observed not only in the hippocampal region, but also in the cortical region. We further evaluated the neuroprotective effect of xanthine oxidoreductase inhibitors in the mouse 3-vessel occlusion model by analyzing changes in the expression of genes regulated by the transcription factor nuclear factor-kappa B (including pro-inflammatory cytokines interleukin-1β (IL-1β) and tumor necrosis factor-α (TNF-α), matrix metalloproteinase-9 and intercellular adhesion molecules-1). Administration of allopurinol resulted in a statistically significant decrease in IL-1β and TNF-α mRNA expression, whereas febuxostat had no significant effect on expression of these genes; nevertheless, both inhibitors effectively reduced serum uric acid concentration. It is suggested that the neuroprotective effect of allopurinol is derived not from inhibition of reactive oxygen species production by xanthine oxidoreductase, but rather from a direct free-radical-scavenging effect.

Indexed as

AldehydesAllopurinolAnimalsBiomarkersBrainBrain IschemiaDisease Models, AnimalInterleukin-1betaMaleMatrix Metalloproteinase 9MiceMice, Inbred C57BLNeuroprotective AgentsNF-kappa BOxidative StressReactive Oxygen Species3-nitrotyrosine4-hydroxy-2-nonenalAldehydesAllopurinolBiomarkersInterleukin-1betaMatrix Metalloproteinase 9Neuroprotective AgentsNF-kappa BReactive Oxygen SpeciesRNA, MessengerTumor Necrosis Factor-alphaTyrosineUric AcidXanthine Dehydrogenase

Identifiers

PMID26230326
PMCPMC4521791
OpenAlexW960013482

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.