Evidence map›Paper›PMID 17021181›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2006

M-like K+ currents in type I hair cells and calyx afferent endings of the developing rat utricle.

Karen M Hurley, Sophie Gaboyard, Meng Zhong, Steven D Price, Julian R A Wooltorton, Anna Lysakowski, Ruth Anne Eatock

Open access · bronzeAbstract readComparative Study
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 72 papers.

0numbers the graph read from it
0cells of the map it votes in
72citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

72 citing papers in PubMed, 116 citations in OpenAlex.

  1. Article
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  8. The potassium channel subunit KbioRxiv : the preprint server for biology · 2024
    Article
  9. Article
  10. Article
  11. Article
  12. Expression of hyperpolarization-activated current (Journal of neurophysiology · 2023
    Article
  13. Article
  14. Nonquantal transmission at the vestibular hair cell-calyx synapse: KProceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  15. Article
  16. Article
  17. Article
  18. Current Response in CaFrontiers in neuroscience · 2021
    Article
  19. Article
  20. Dopaminergic Inhibition of NaFrontiers in neuroscience · 2021
    Article

12 more citing papers are in PubMed but not listed here.

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

7 authors at 3 institutions in 1 country.

Karen M HurleyThe Bobby R. Alford Department of Otorhinolaryngology, Head and Neck Surgery, Baylor College of Medicine, Houston, Texas 77030, USA.
Sophie Gaboyard
Meng Zhong
Steven D Price
Julian R A Wooltorton
Anna Lysakowski
Ruth Anne Eatock
University of Illinois Chicago · USBaylor College of Medicine · USHarvard University Press · US

Funding

Stimulus processing in mammalian vestibular organsR01DC002290 · NIDCD · MASSACHUSETTS EYE AND EAR INFIRMARY · PI EATOCK, RUTH ANNE · 1994 to 2012
$5.4M
NIDCD NIH HHS DC002290NIDCD NIH HHS R01 DC002290
6 · The paper itself

Abstract

Type I vestibular hair cells have large K+ currents that, like neuronal M currents, activate negative to resting potential and are modulatable. In rodents, these currents are acquired postnatally. In perforated-patch recordings from rat utricular hair cells, immature hair cells [younger than postnatal day 7 (P7)] had a steady-state K+ conductance (g(-30)) with a half-activation voltage (V1/2) of -30 mV. The size and activation range did not change in maturing type II cells, but, by P16, type I cells had added a K conductance that was on average fourfold larger and activated much more negatively. This conductance may comprise two components: g(-60) (V1/2 of -60 mV) and g(-80) (V1/2 of -80 mV). g(-80) washed out during ruptured patch recordings and was blocked by a protein kinase inhibitor. M currents can include contributions from KCNQ and ether-a-go-go-related (erg) channels. KCNQ and erg channel blockers both affected the K+ currents of type I cells, with KCNQ blockers being more potent at younger than P7 and erg blockers more potent at older than P16. Single-cell reverse transcription-PCR and immunocytochemistry showed expression of KCNQ and erg subunits. We propose that KCNQ channels contribute to g(-30) and g(-60) and erg subunits contribute to g(-80). Type I hair cells are contacted by calyceal afferent endings. Recordings from dissociated calyces and afferent endings revealed large K+ conductances, including a KCNQ conductance. Calyx endings were strongly labeled by KCNQ4 and erg1 antisera. Thus, both hair cells and calyx endings have large M-like K+ conductances with the potential to control the gain of transmission.

Indexed as

AnimalsAnimals, NewbornHair Cells, VestibularIn Vitro TechniquesKCNQ Potassium ChannelsNerve EndingsNeurons, AfferentPotassium Channel BlockersPotassium ChannelsRatsRats, Long-EvansSaccule and UtricleKCNQ Potassium ChannelsPotassium Channel BlockersPotassium Channels

Identifiers

PMID17021181
PMCPMC6674627
OpenAlexW2062319567

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.