Evidence map›Paper›PMID 9660893›Full record

ArticleThe Journal of physiology1998

Mutual occlusion of P2X ATP receptors and nicotinic receptors on sympathetic neurons of the guinea-pig.

T J Searl, R S Redman, E M Silinsky

Open access · greenAbstract read
In one paragraph

Article in The Journal of physiology, 1998. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
2.5field-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

25 citing papers in PubMed, 76 citations in OpenAlex.

  1. Extracellular ATP Neurotransmission and Nicotine Sex-Specifically Modulate Habenular Neuronal Activity in Adolescence.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2023
    Article
  2. P2X receptors.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2016
    Review
  3. Article
  4. Article
  5. Review
  6. Review
  7. Article
  8. Neuronal P2X2 receptors are mobile ATP sensors that explore the plasma membrane when activated.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2011
    Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Interaction of P2 purinergic receptors with cellular macromolecules.Naunyn-Schmiedeberg's archives of pharmacology · 2008
    Review
  14. Article
  15. Article
  16. Molecular properties of P2X receptors.Pflugers Archiv : European journal of physiology · 2006
    Review
  17. Article
  18. Article
  19. Article
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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

3 authors at 1 institution in 1 country.

T J SearlDepartment of Molecular Pharmacology, Northwestern University Medical School, 303 East Chicago Avenue, Chicago, IL 60611, USA.
R S Redman
E M Silinsky
Northwestern University · US

Funding

ADENOSINE DERIVATIVES AND TRANSMITTER RELEASER01NS012782 · NINDS · NORTHWESTERN UNIVERSITY · PI SILINSKY, EUGENE M · 1985 to 2003
$1.5M
NINDS NIH HHS NS12782NINDS NIH HHS R01 NS012782
6 · The paper itself

Abstract

1. The interaction of ion channels activated by nicotinic receptor agonists with ion channels gated by extracellular ATP (i.e. P2X receptors) was studied on sympathetic neurons acutely dissociated from coeliac ganglia of the guinea-pig. Patch clamp methods were used to measure the inward current generated through these non-selective cationic channels under voltage clamp. 2. At the whole cell level, the specific nicotinic receptor agonists nicotine (5-100 microM) or cytisine (50-75 microM) and the P2X receptor agonists ATP (0.1-7 microM) or alpha,beta-methylene ATP (6 microM) were examined separately and in the presence of the other receptor activator. When a nicotinic and P2X receptor agonist were applied together, mutually occlusive effects were generally observed. This occurred even with concentrations of agonists that in themselves generated little to no inward current. 3. The occlusive effects of nicotinic agonists on ATP-gated currents were blocked by the nicotinic receptor/ion channel blocker hexamethonium (150 microM). The occlusive effects of ATP analogues on inward currents generated by nicotinic agonists were blocked by the P2X receptor antagonist suramin (100 microM). 4. Mutual occlusion of the effects of nicotinic agonists and ATP analogues were also observed when currents through single channels were studied in excised (outside-out) patches. 5. The results suggest that nicotinic receptors and P2X ATP receptors do not act independently in these sympathetic neurons.

Indexed as

Adenosine TriphosphateAnimalsElectric StimulationElectrophysiologyGuinea PigsIn Vitro TechniquesMaleMembrane PotentialsNeuronsNicotineNicotinic AgonistsPatch-Clamp TechniquesPurinergic P2 Receptor AgonistsPurinergic P2 Receptor AntagonistsReceptors, NicotinicReceptors, Purinergic P2Adenosine TriphosphateNicotineNicotinic AgonistsPurinergic P2 Receptor AgonistsPurinergic P2 Receptor AntagonistsReceptors, NicotinicReceptors, Purinergic P2Receptors, Purinergic P2X

Identifiers

PMID9660893
PMCPMC2231072
OpenAlexW2033229260

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.