Evidence map›Paper›PMID 30366010›Full record

ArticleNeuroscience letters2019

Characterization of the antagonist actions of 5-BDBD at the rat P2X4 receptor.

Claudio Coddou, Rodrigo Sandoval, María José Hevia, Stanko S Stojilkovic

Abstract read
In one paragraph

Article in Neuroscience letters, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

24 citing papers in PubMed, 43 citations in OpenAlex.

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  8. Modulation of P2XPhysiological reports · 2022
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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

4 authors at 2 institutions in 2 countries.

Claudio CoddouDepartmento de Ciencias Biomédicas, Facultad de Medicina, Universidad Católica del Norte, Coquimbo, Chile; Section on Cellular Signaling, TheEunice Kennedy ShiverNational Institute of Health and Human Development, National Institutes of Health, Bethesda, MD 20892, United States. Electronic address: ccoddou@ucn.cl.
Rodrigo SandovalDepartmento de Ciencias Biomédicas, Facultad de Medicina, Universidad Católica del Norte, Coquimbo, Chile.
María José HeviaDepartmento de Ciencias Biomédicas, Facultad de Medicina, Universidad Católica del Norte, Coquimbo, Chile.
Stanko S StojilkovicSection on Cellular Signaling, TheEunice Kennedy ShiverNational Institute of Health and Human Development, National Institutes of Health, Bethesda, MD 20892, United States.
Universidad Católica del Norte · CLNational Institutes of Health · US

Funding

Intracellular Signaling In Endocrine CellsZIAHD000195 · NICHD · EUNICE KENNEDY SHRIVER NATIONAL INSTITUTE OF CHILD HEALTH & HUMAN DEVELOPMENT · PI STOJILKOVIC, STANKO S. · 2009 to 2025
$18.8M
Intramural NIH HHS Z99 HD999999Intramural NIH HHS ZIA HD000195
6 · The paper itself

Abstract

P2X receptors (P2XRs) are a family of ATP-gated ionic channels that are expressed in numerous excitable and non-excitable cells. Despite the great advance on the structure and function of these receptors in the last decades, there is still lack of specific and potent antagonists for P2XRs subtypes, especially for the P2X4R. Here, we studied in detail the effect of the P2X4R antagonist 5-(3-bromophenyl)-1,3-dihydro-2H-benzofuro[3,2-e]-1,4-diazepin-2-one (5-BDBD) on ATP-induced currents mediated by the rat P2X4R and compared its specificity among another rat P2XRs. We found that 5-BDBD is a potent P2X4R antagonist, with an IC

Indexed as

Adenosine TriphosphateAnimalsBenzodiazepinonesCells, CulturedDose-Response Relationship, DrugHippocampusHumansLong-Term PotentiationMalePurinergic P2X Receptor AntagonistsRatsReceptors, Purinergic P2X5-(3-bromophenyl)-1,3-dihydro-2H-benzofuro(3,2-e)-1,4-diazepin-2-oneAdenosine TriphosphateBenzodiazepinonesPurinergic P2X Receptor AntagonistsReceptors, Purinergic P2X5-BDBDLong-term potentiationP2X4 receptorPurinergic signaling

Identifiers

PMID30366010
PMCPMC6320288
OpenAlexW2897079566

What OpenQuestion holds

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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.