Evidence map›Paper›PMID 17664346›Full record

ArticleThe Journal of general physiology2007

Responses of rat P2X2 receptors to ultrashort pulses of ATP provide insights into ATP binding and channel gating.

Luciano Moffatt, Richard I Hume

Open access · greenAbstract read
In one paragraph

Article in The Journal of general physiology, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.7field-weighted citation impact, top 17% 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

18 citing papers in PubMed, 32 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. The Dynamic Behavior of the P2XBiophysical journal · 2016
    Article
  8. Article
  9. Review
  10. Exploring the ATP-binding site of P2X receptors.Frontiers in cellular neuroscience · 2013
    Review
  11. Review
  12. Article
  13. Review
  14. Article
  15. touché Is required for touch-evoked generator potentials within vertebrate sensory neurons.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2010
    Article
  16. Article
  17. Article
  18. 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 2 institutions in 2 countries.

Luciano MoffattDepartment of Molecular, Cellular, and Developmental Biology, University of Michigan, Ann Arbor, MI 48109, USA. lmoffatt@qi.fcen.uba.ar
Richard I Hume
University of Buenos Aires · ARUniversity of Michigan–Ann Arbor · US

Funding

STUDIES OF P2X ATP RECEPTORSR01NS039196 · NINDS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI HUME, RICHARD IRWIN · 2001 to 2009
$2.6M
NINDS NIH HHS NS 039196NINDS NIH HHS R01 NS039196
6 · The paper itself

Abstract

To gain insight into the way that P2X(2) receptors localized at synapses might function, we explored the properties of outside-out patches containing many of these channels as ATP was very rapidly applied and removed. Using a new method to calibrate the speed of exchange of solution over intact patches, we were able to reliably produce applications of ATP lasting <200 micros. For all concentrations of ATP, there was a delay of at least 80 micros between the time when ATP arrived at the receptor and the first detectable flow of inward current. In response to 200-micros pulses of ATP, the time constant of the rising phase of the current was approximately 600 micros. Thus, most channel openings occurred when no free ATP was present. The current deactivated with a time constant of approximately 60 ms. The amplitude of the peak response to a brief pulse of a saturating concentration of ATP was approximately 70% of that obtained during a long application of the same concentration of ATP. Thus, ATP leaves fully liganded channels without producing an opening at least 30% of the time. Extensive kinetic modeling revealed three different schemes that fit the data well, a sequential model and two allosteric models. To account for the delay in opening at saturating ATP, it was necessary to incorporate an intermediate closed state into all three schemes. These kinetic properties indicate that responses to ATP at synapses that use homomeric P2X(2) receptors would be expected to greatly outlast the duration of the synaptic ATP transient produced by a single presynaptic spike. Like NMDA receptors, P2X(2) receptors provide the potential for complex patterns of synaptic integration over a time scale of hundreds of milliseconds.

Indexed as

Adenosine TriphosphateAnimalsCell LineDose-Response Relationship, DrugElectrophysiologyHumansIon Channel GatingModels, BiologicalPatch-Clamp TechniquesProtein BindingRatsReceptors, Purinergic P2Receptors, Purinergic P2X2SynapsesTime FactorsAdenosine TriphosphateP2RX2 protein, humanP2rx2 protein, ratReceptors, Purinergic P2Receptors, Purinergic P2X2

Identifiers

PMID17664346
PMCPMC2151634
OpenAlexW2067256827

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.