Evidence map›Paper›PMID 20972559›Full record

ArticleThe Journal of membrane biology2010

Pharmacological properties and physiological function of a P2X-like current in single proximal tubule cells isolated from frog kidney.

John P Davies, Louise Robson

Open access · hybridAbstract read
In one paragraph

Article in The Journal of membrane biology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.7field-weighted citation impact, top 29% 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

2 citing papers in PubMed, 3 citations in OpenAlex.

  1. Review
  2. 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

2 authors at 1 institution in 1 country.

John P DaviesDepartment of Biomedical Science, University of Sheffield, Sheffield S102TN, UK.
Louise Robson
University of Sheffield · GB

Funding

Wellcome Trust
6 · The paper itself

Abstract

Although previous studies have provided evidence for the expression of P2X receptors in renal proximal tubule, only one cell line study has provided functional evidence. The current study investigated the pharmacological properties and physiological role of native P2X-like currents in single frog proximal tubule cells using the whole-cell patch-clamp technique. Extracellular ATP activated a cation conductance (P2X(f)) that was also Ca²+-permeable. The agonist sequence for activation was ATP = αβ-MeATP > BzATP = 2-MeSATP, and P2X(f) was inhibited by suramin, PPADS and TNP-ATP. Activation of P2X(f) attenuated the rundown of a quinidine-sensitive K+ conductance, suggesting that P2X(f) plays a role in K+ channel regulation. In addition, ATP/ADP apyrase and inhibitors of P2X(f) inhibited regulatory volume decrease (RVD). These data are consistent with the presence of a P2X receptor that plays a role in the regulation of cell volume and K+ channels in frog renal proximal tubule cells.

Indexed as

Adenosine TriphosphateAnimalsCells, CulturedKidneyKidney Tubules, ProximalPatch-Clamp TechniquesPurinergic AgonistsPurinergic AntagonistsPyridoxal PhosphateRana temporariaReceptors, Purinergic P2XThionucleotides2',3'-O-(2,4,6-trinitro-cyclohexadienylidine)adenosine 5'-triphosphate2-methylthio-ATP3'-O-(4-benzoyl)benzoyladenosine 5'-triphosphateAdenosine TriphosphatePurinergic AgonistsPurinergic AntagonistsPyridoxal Phosphatepyridoxal phosphate-6-azophenyl-2',4'-disulfonic acidReceptors, Purinergic P2XThionucleotides

Identifiers

PMID20972559
PMCPMC2990016
OpenAlexW2036655426

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.