Evidence map›Paper›PMID 24200924›Full record

ArticleNeuroscience2014

Heterogeneous intrinsic excitability of murine spiral ganglion neurons is determined by Kv1 and HCN channels.

Q Liu, E Lee, R L Davis

Abstract read
In one paragraph

Article in Neuroscience, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
3.4field-weighted citation impact, top 7% 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

34 citing papers in PubMed, 47 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Modulation of potassium conductances optimizes fidelity of auditory information.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  5. Low-voltage Activating KExperimental neurobiology · 2022
    Article
  6. Article
  7. Article
  8. Article
  9. Dynamic Heterogeneity Shapes Patterns of Spiral Ganglion Activity.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2021
    Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. CaBP1 regulates CaMolecular and cellular neurosciences · 2018
    Article
  20. Review
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.

Q LiuDepartment of Cell Biology and Neuroscience, Rutgers University, Piscataway, NJ 08854, USA.
E LeeRutgers University, New Jersey Medical School, Newark, NJ 07746, USA.
R L DavisDepartment of Cell Biology and Neuroscience, Rutgers University, Piscataway, NJ 08854, USA. Electronic address: rldavis@rci.rutgers.edu.
Rutgers, The State University of New Jersey · US

Funding

ION CHANNEL DIVERSITY IN PRIMARY AUDITORY NEURONSR01DC001856 · NIDCD · RUTGERS THE ST UNIV OF NJ NEW BRUNSWICK · PI DAVIS, ROBIN L. · 1998 to 2019
$5.9M
NIDCD NIH HHS R01 DC001856NIDCD NIH HHS R01 DC01856
6 · The paper itself

Abstract

The spiral ganglion conveys afferent auditory information predominantly through a single class of type I neurons that receive signals from inner hair cell sensory receptors. These auditory primary afferents, like in other systems (Puopolo and Belluzzi, 1998; Gascon and Moqrich, 2010; Leao et al., 2012) possess a marked diversity in their electrophysiological features (Taberner and Liberman, 2005). Consistent with these observations, when the auditory primary afferents were assessed in neuronal explants separated from their peripheral and central targets it was found that individual neurons were markedly heterogeneous in their endogenous electrophysiological features. One aspect of this heterogeneity, obvious throughout the ganglion, was their wide range of excitability as assessed by voltage threshold measurements (Liu and Davis, 2007). Thus, while neurons in the base differed significantly from apical and middle neurons in their voltage thresholds, each region showed distinctly wide ranges of values. To determine whether the resting membrane potentials (RMPs) of these neurons correlate with the threshold distribution and to identify the ion channel regulatory elements underlying heterogeneous neuronal excitability in the ganglion, patch-clamp recordings were made from postnatal day (P5-8) murine spiral ganglion neurons in vitro. We found that RMP mirrored the tonotopic threshold distribution, and contributed an additional level of heterogeneity in each cochlear location. Pharmacological experiments further indicated that threshold and RMP was coupled through the Kv1 current, which had a dual impact on both electrophysiological parameters. Whereas, hyperpolarization-activated cationic channels decoupled these two processes by primarily affecting RMP without altering threshold level. Thus, beyond mechanical and synaptic specializations, ion channel regulation of intrinsic membrane properties imbues spiral ganglion neurons with different excitability levels, a feature that contributes to primary auditory afferent diversity.

Indexed as

4-AminopyridineAnimalsAnimals, NewbornBiophysical PhenomenaBiophysicsCadmium ChlorideElapid VenomsElectric StimulationHyperpolarization-Activated Cyclic Nucleotide-Gated ChannelsMembrane PotentialsMiceMice, Inbred C57BLNeuronsNeurotoxinsPatch-Clamp TechniquesPotassium Channel Blockers4-AminopyridineCadmium ChloridedendrotoxinElapid VenomsHyperpolarization-Activated Cyclic Nucleotide-Gated ChannelsNeurotoxinsPotassium Channel BlockersShaker Superfamily of Potassium ChannelsTetrodotoxin4-(2-hydroxyethyl)piperazine-1-ethanesulfonic acid4-aminopyridine4-APanalysis of varianceANOVAauditorycadmium chlorideCdCl(2)cesium chlorideCsCldays in vitrodendrotoxinDIVDTXEGTAEPSPethylene glycol tetraacetic acidexcitatory postsynaptic potentialHCNHEPEShyperpolarization-activated cationic channelhyperpolarization-activated cationic currentI(h)IHCinner hair cellintrinsic excitabilityK(v)1PBSphosphate-buffered salineresting membrane potentialRMPSAslowly accommodatingspiral ganglion neuronspontaneous discharge rateSRTEAtetraethylammoniumtetrodotoxinTTXvoltage thresholdV(θ)

Identifiers

PMID24200924
PMCPMC3897933
OpenAlexW2020426036

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.