Evidence map›Paper›PMID 14522840›Full record

ReviewBritish journal of pharmacology2003

Novel data point to a broader mechanism of action of oxidized ATP: the P2X7 receptor is not the only target.

Francesco Di Virgilio

Open access · bronzeAbstract readCommentReview
In one paragraph

Review in British journal of pharmacology, 2003. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
3.0field-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

28 citing papers in PubMed, 66 citations in OpenAlex.

  1. Review
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  6. Article
  7. Review
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  9. Article
  10. Review
  11. P2XFrontiers in cellular neuroscience · 2021
    Review
  12. Article
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  15. Article
  16. Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

1 author at 1 institution in 1 country.

Francesco Di VirgilioDepartment of Experimental and Diagnostic Medicine, University of Ferrara, Via Borsari 46, I-44100 Ferrara, Italy. fdv@unife.it
University of Ferrara · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Oxidized ATP (oATP) is a Schiff-base-forming reagent that has been used for some years as an antagonist at the P2X7 receptor (P2X7R). Preincubation of mononuclear phagocytes with this inhibitor leads to attenuation of several proinflammatory responses triggered by extracellular ATP as well as a few non-nucleotide agonists. Novel data show that oATP reduces NFkappaB activation and IL-8 release in cells lacking P2X7R, thus suggesting that some anti-inflammatory effects of oATP may not be due to blockade of the P2X7R. This effect of oATP resembles the action of other natural or synthetic Schiff-base-forming reagents with immunomodulatory activity.

Indexed as

Adenosine TriphosphateAnimalsHumansOxidation-ReductionPurinergic P2 Receptor AntagonistsReceptors, Purinergic P2Receptors, Purinergic P2X7Adenosine TriphosphateP2RX7 protein, humanPurinergic P2 Receptor AntagonistsReceptors, Purinergic P2Receptors, Purinergic P2X7

Identifiers

PMID14522840
PMCPMC1574057
OpenAlexW2012885754

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.