Evidence map›Paper›PMID 18174213›Full record

ArticleThe Journal of physiology2008

Biophysical properties of CaV1.3 calcium channels in gerbil inner hair cells.

Stuart L Johnson, Walter Marcotti

Open access · greenAbstract read
In one paragraph

Article in The Journal of physiology, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed
2.5field-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

44 citing papers in PubMed, 78 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Synaptic Contributions to Cochlear Outer Hair Cell CaThe Journal of neuroscience : the official journal of the Society for Neuroscience · 2021
    Article
  5. Review
  6. Current Response in CaFrontiers in neuroscience · 2021
    Article
  7. RBP2 stabilizes slow Cav1.3 CaPflugers Archiv : European journal of physiology · 2020
    Article
  8. Hair Cell Afferent Synapses: Function and Dysfunction.Cold Spring Harbor perspectives in medicine · 2019
    Review
  9. How to Build a Fast and Highly Sensitive Sound Detector That Remains Robust to Temperature Shifts.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2019
    Article
  10. Article
  11. Clustered CaCell reports · 2018
    Article
  12. Article
  13. Review
  14. The Coupling between CaThe Journal of neuroscience : the official journal of the Society for Neuroscience · 2017
    Article
  15. Article
  16. Article
  17. EF-hand protein Ca2+ buffers regulate Ca2+ influx and exocytosis in sensory hair cells.Proceedings of the National Academy of Sciences of the United States of America · 2015
    Article
  18. Article
  19. Review
  20. ATP hydrolysis is critically required for function of CaV1.3 channels in cochlear inner hair cells via fueling Ca2+ clearance.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2014
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

2 authors at 1 institution in 1 country.

Stuart L JohnsonDepartment of Biomedical Science, University of Sheffield, Sheffield S10 2TN, UK.
Walter Marcotti
University of Sheffield · GB

Funding

Wellcome Trust 077333
6 · The paper itself

Abstract

The Ca(2+) current (I(Ca)) in prehearing and adult inner hair cells (IHCs), the primary sensory receptors of the mammalian cochlea, is mainly carried by L-type (Ca(V)1.3) Ca(2+) channels. I(Ca) in immature and adult IHCs triggers the release of neurotransmitter onto auditory afferent fibres in response to spontaneous action potentials (APs) or graded receptor potentials, respectively. We have investigated whether the biophysical properties of I(Ca) vary between low- and high-frequency IHCs during cochlear development and whether its inactivation influences cellular responses. I(Ca) was recorded from gerbil IHCs maintained near physiological recording conditions. The size of I(Ca) in adult IHCs was about a third of that in immature cells with no apparent difference along the cochlea at both stages. The activation kinetics of I(Ca) were significantly faster in high-frequency IHCs, with that of adult cells being more rapid than immature cells. The degree of I(Ca) inactivation was similar along the immature cochlea but larger in high- than low-frequency adult IHCs. This inactivation was greatly reduced with barium but not affected by changing the intracellular buffer (BAPTA instead of EGTA). Immature basal IHCs showed faster recovery of I(Ca) from inactivation than apical cells allowing them to support a higher AP frequency. I(Ca) in adult IHCs was more resistant to progressive inactivation following repeated voltage stimulation than that of immature cells. This suggests that adult IHCs are likely to be suited for sustaining rapid and repeated release of synaptic vesicles, which is essential for sound encoding.

Indexed as

BiophysicsAcoustic StimulationAction PotentialsAnimalsBiophysical PhenomenaCalciumCalcium Channels, L-TypeCochleaGerbillinaeHair Cells, Auditory, InnerMembrane PotentialsPatch-Clamp TechniquesCalciumCalcium Channels, L-Type

Identifiers

PMID18174213
PMCPMC2268984
OpenAlexW1750536826

What OpenQuestion holds

Textmetadata
LicenceTDM
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.