Evidence map›Paper›PMID 11717350›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2001

P2X2 receptor mediates stimulation of parasensory cation absorption by cochlear outer sulcus cells and vestibular transitional cells.

J H Lee, T Chiba, D C Marcus

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2001. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
2.7field-weighted citation impact, top 11% 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

39 citing papers in PubMed, 89 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Progress in protecting vestibular hair cells.Archives of toxicology · 2021
    Review
  5. Article
  6. QTL Mapping of Endocochlear Potential Differences between C57BL/6J and BALB/cJ mice.Journal of the Association for Research in Otolaryngology : JARO · 2016
    Article
  7. Review
  8. Article
  9. Article
  10. Mechanisms of otoconia and otolith development.Developmental dynamics : an official publication of the American Association of Anatomists · 2015
    Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. Critical roles of transitional cells and Na/K-ATPase in the formation of vestibular endolymph.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2011
    Article
  17. Review
  18. Article
  19. The role of pendrin in the development of the murine inner ear.Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology · 2011
    Review
  20. 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

3 authors at 1 institution in 1 country.

J H LeeDepartment of Anatomy and Physiology, Kansas State University, Manhattan, Kansas 66506, USA.
T Chiba
D C Marcus
Kansas State University · US

Funding

COCHLEAR AND VESTIBULAR ION TRANSPORTR01DC000212 · NIDCD · KANSAS STATE UNIVERSITY · PI MARCUS, DANIEL C · 1988 to 2009
$3.1M
NIDCD NIH HHS 5R01-DC00212
6 · The paper itself

Abstract

Cochlear outer sulcus cells (OSC) and vestibular transitional cells (VTC) are part of the parasensory epithelium in the inner ear and are located in homologous positions between the sensory hair cells and the cation secretory epithelial cells in the cochlea and the vestibular labyrinth. OSC are known to sustain a reabsorptive transepithelial current and to contain an immunoreactivity for P2X(2) purinergic receptors. This study addresses whether OSC and VTC share functional similarities and extends this hypothesis to the question of whether both cell types contain functional P2X(2) receptors. The current density (I(sc)) was recorded with the vibrating probe technique and was found to be similar in VTC and OSC. Both gadolinium and flufenamic acid reduced I(sc) in VTC, as reported previously for OSC. I(sc) was stimulated by extracellular ATP but not by selective agonists of P2Y receptors. Purinergic receptor agonists increased I(sc) with a potency order of ATP > 2'- and 3'-O-(4-benzoyl-benzoyl)adenosine 5'-triphosphate alpha,beta-methyleneadenosine 5'-triphosphate in both OSC and VTC. In the presence of suramin (100 micrometer) or gadolinium (100 micrometer), the responses of ATP were inhibited significantly in both OSC and VTC. This pharmacological profile is consistent with that of the P2X(2) receptor. These results demonstrate that VTC participate in vestibular parasensory cation absorption and that both OSC and VTC regulate their parasensory cation flux via P2X(2) receptors, which would regulate the endolymphatic concentration of the current-carrying ion species in auditory and vestibular transduction.

Indexed as

Adenosine DiphosphateAdenosine TriphosphateAnimalsCationsCochleaDiffusion Chambers, CultureDose-Response Relationship, DrugFlufenamic AcidGadoliniumGerbillinaeHearingIn Vitro TechniquesIon ChannelsIon TransportMicroelectrodesPhysical StimulationAdenosine DiphosphateAdenosine TriphosphateCationsFlufenamic AcidGadoliniumIon ChannelsPurinergic P2 Receptor AgonistsPurinergic P2 Receptor AntagonistsReceptors, Purinergic P2Receptors, Purinergic P2X2SuraminUridine DiphosphateUridine Triphosphate

Identifiers

PMID11717350
PMCPMC6763907
OpenAlexW1863695291

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.