Evidence map›Paper›PMID 20407915›Full record

ArticleJournal of the Association for Research in Otolaryngology : JARO2010

K+ currents in isolated vestibular afferent calyx terminals.

Ritu Dhawan, Scott E Mann, Frances L Meredith, Katherine J Rennie

Open access · bronzeAbstract read
In one paragraph

Article in Journal of the Association for Research in Otolaryngology : JARO, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.0field-weighted citation impact, top 30% 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

17 citing papers in PubMed, 25 citations in OpenAlex.

  1. Article
  2. Expression of hyperpolarization-activated current (Journal of neurophysiology · 2023
    Article
  3. Dopaminergic Inhibition of NaFrontiers in neuroscience · 2021
    Article
  4. Persistent and resurgent NaJournal of neurophysiology · 2020
    Article
  5. KNeuroscience · 2020
    Article
  6. Regional and Developmental Differences in NaFrontiers in cellular neuroscience · 2018
    Article
  7. Article
  8. Article
  9. Accumulation of KThe Journal of physiology · 2017
    Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. 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

4 authors at 2 institutions in 1 country.

Ritu DhawanDepartment of Otolaryngology, University of Colorado Denver, Anschutz Medical Campus, 12700 E. 19th Avenue, Aurora, CO 80045, USA.
Scott E Mann
Frances L Meredith
Katherine J Rennie
University of Colorado Anschutz Medical Campus · USUniversity of Colorado Denver · US

Funding

NEUROSCIENCE TRAINING GRANTT32HD041697 · NICHD · UNIVERSITY OF COLORADO DENVER · PI RESTREPO, DIEGO · 2001 to 2015
$2.4M
Neurotransmission at the vestibular calyx synapseR01DC008297 · NIDCD · UNIVERSITY OF COLORADO DENVER · PI RENNIE, KATHERINE JANET · 2007 to 2009
$819k
Neurotransmission at the vestibular calyx synapseR55DC008297 · NIDCD · UNIVERSITY OF COLORADO DENVER · PI RENNIE, KATHERINE J. · 2007 to 2007
$100k
NICHD NIH HHS HD41697NICHD NIH HHS T32 HD041697NIDCD NIH HHS DC008297NIDCD NIH HHS R01 DC008297NIDCD NIH HHS R55 DC008297
6 · The paper itself

Abstract

Vestibular hair cells transduce mechanical displacements of their hair bundles into an electrical receptor potential which modulates transmitter release and subsequent action potential firing in afferent neurons. To probe ionic mechanisms underlying sensory coding in vestibular calyces, we used the whole-cell patch-clamp technique to record action potentials and K(+) currents from afferent calyx terminals isolated from the semicircular canals of Mongolian gerbils. Calyx terminals showed minimal current at the mean zero-current potential (-60 mV), but two types of outward K(+) currents were identified at potentials above -50 mV. The first current was a rapidly activating and inactivating K(+) current that was blocked by 4-aminopyridine (4-AP, 2.5 mM) and BDS-I (up to 250 nM). The time constant for activation of this current decreased with membrane depolarization to a minimum value of approximately 1 ms. The 4-AP-sensitive current showed steady-state inactivation with a half-inactivation of approximately -70 mV. A second, more slowly activating current (activation time constant was 8.5 +/- 0.7 ms at -8 mV) was sensitive to TEA (30 mM). The TEA-sensitive current also showed steady-state inactivation with a half-inactivation of -95.4 +/- 1.4 mV, following 500-ms duration conditioning pulses. A combination of 4-AP and TEA blocked approximately 90% of the total outward current. In current clamp, single Na(+)-dependent action potentials were evoked following hyperpolarization to potentials more negative than the resting potential. 4-AP application increased action potential width, whereas TEA both increased the width and greatly reduced repolarization of the action potential.

Indexed as

Action PotentialsAnimalsGerbillinaeHair Cells, AmpullaHair Cells, VestibularPatch-Clamp TechniquesPotassiumPotassium Channel BlockersSynapsesPotassiumPotassium Channel Blockers

Identifiers

PMID20407915
PMCPMC2914245
OpenAlexW2017689163

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.