Evidence map›Paper›PMID 9824710›Full record

ArticleThe Journal of physiology1998

Non-additive interaction between nicotinic cholinergic and P2X purine receptors in guinea-pig enteric neurons in culture.

X Zhou, J J Galligan

Open access · bronzeAbstract 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 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
1.9field-weighted citation impact, top 13% 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

36 citing papers in PubMed, 109 citations in OpenAlex.

  1. Article
  2. Review
  3. P2X receptors.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2016
    Review
  4. Article
  5. Review
  6. Review
  7. Review
  8. Article
  9. 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
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Interaction of P2 purinergic receptors with cellular macromolecules.Naunyn-Schmiedeberg's archives of pharmacology · 2008
    Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

2 authors at 1 institution in 1 country.

X ZhouDepartment of Pharmacology and Toxicology and the Neuroscience Program, Michigan State University, East Lansing, MI,, USA. zhoux@pilot.msu.edu
J J Galligan
Michigan State University · US

Funding

MECHANISMS OF SLOW SYNAPTIC EXCITATION IN ENTERIC NERVESK04NS001738 · NINDS · MICHIGAN STATE UNIVERSITY · PI GALLIGAN, JAMES J. · 1994 to 1998
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MECHANISMS OF SLOW SYNAPTIC EXCITATION IN ENTERIC NERVESR01NS033289 · NINDS · MICHIGAN STATE UNIVERSITY · PI GALLIGAN, JAMES J. · 1995 to 1999
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NINDS NIH HHS NS01738NINDS NIH HHS NS33289
6 · The paper itself

Abstract

1. Acetylcholine (ACh)-activated currents and their interaction with ATP-activated currents were studied in primary cultures of myenteric neurons from guinea-pig small intestine using patch clamp techniques. Peak currents caused by co-application of ACh (1 mM) and ATP (300 microM) were 78 +/- 2 % of the sum of currents activated by each agonist alone (P < 0.05, n = 29). Reversal potentials measured during co-application of ACh and ATP did not differ from those measured during application of ACh or ATP alone. Addition of BAPTA (10 mM) to the pipette solution or replacement of extracellular Ca2+ with Na+ did not prevent occlusion. 2. Responses caused by co-application of 5-HT (300 microM), acting at 5-HT3 receptors, and ACh (3 mM) or ATP (1 mM) were additive (94 +/- 3 or 96 +/- 4 %, respectively, of the sum of currents activated by 5-HT and ACh or ATP alone; P > 0.05). Currents caused by GABA (1 mM), acting at GABAA receptors, and ACh (3 mM) or ATP (1 mM) were also additive (105 +/- 4 or 100 +/- 3 %, respectively, of the sum of currents activated by GABA and ACh or GABA and ATP applied separately; P > 0. 05). 3. Single channel currents caused by ACh and ATP in the same outside-out patches were less than additive (85 +/- 10 % of the predicted sum, P < 0.05). 4. P2X receptors and nicotinic cholinergic receptors (nAChRs) are linked in a mutually inhibitory manner in guinea-pig myenteric neurons. The functional interaction does not involve ligand binding sites, Ca2+-dependent mechanisms, a change in the driving force for Na+ or cytoplasmic signalling mechanisms.

Indexed as

AcetylcholineAdenosine TriphosphateAnimalsCationsCells, CulturedElectric StimulationElectrophysiologyGuinea PigsIntestinal MucosaIon Channel GatingIon ChannelsKineticsMembrane PotentialsNeuronsNicotinic AgonistsNicotinic AntagonistsAcetylcholineAdenosine TriphosphateCationsIon ChannelsNicotinic AgonistsNicotinic AntagonistsPurinergic P2 Receptor AgonistsPurinergic P2 Receptor AntagonistsReceptors, NicotinicReceptors, Purinergic P2Receptors, Serotonin

Identifiers

PMID9824710
PMCPMC2231316
OpenAlexW2114926262

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.