Evidence map›Paper›PMID 33244141›Full record

ArticleScientific reports2020

Ventral cochlear nucleus bushy cells encode hyperacusis in guinea pigs.

David T Martel, Susan E Shore

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.8field-weighted citation impact, top 25% 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

7 citing papers in PubMed, 15 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Too Blind to See the Elephant? Why Neuroscientists Ought to Be Interested in Tinnitus.Journal of the Association for Research in Otolaryngology : JARO · 2021
    Review
  7. 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

2 authors at 1 institution in 1 country.

David T MartelKresge Hearing Research Inst., Department of Otolaryngology, University of Michigan, 1100 W. Medical Center Drive, Ann Arbor, MI, 48109, USA.
Susan E ShoreKresge Hearing Research Inst., Department of Otolaryngology, University of Michigan, 1100 W. Medical Center Drive, Ann Arbor, MI, 48109, USA. sushore@umich.edu.
University of Michigan–Ann Arbor · US

Funding

Sensory Mechanisms and Disorders - Administrative SupplementT32DC000011 · NIDCD · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Michael Thomas Roberts · 1989 to 2026
$9.5M
Function of trigeminal pathways to the cochlear nucleusR01DC004825 · NIDCD · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI SHORE, SUSAN E · 2001 to 2016
$5.5M
Reversing Synchronized Brain Circuits with Targeted Auditory-Somatosensory Stimulation to Treat Phantom PerceptsRF1MH114244 · NIMH · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI SHORE, SUSAN E · 2017 to 2017
$2.4M
NIDCD NIH HHS R01-DC004825NIDCD NIH HHS T32 DC000011NIDCD NIH HHS T32-DC00011NIMH NIH HHS MH114244-01NIMH NIH HHS RF1 MH114244
6 · The paper itself

Abstract

Psychophysical studies characterize hyperacusis as increased loudness growth over a wide-frequency range, decreased tolerance to loud sounds and reduced behavioral reaction time latencies to high-intensity sounds. While commonly associated with hearing loss, hyperacusis can also occur without hearing loss, implicating the central nervous system in the generation of hyperacusis. Previous studies suggest that ventral cochlear nucleus bushy cells may be putative neural contributors to hyperacusis. Compared to other ventral cochlear nucleus output neurons, bushy cells show high firing rates as well as lower and less variable first-spike latencies at suprathreshold intensities. Following cochlear damage, bushy cells show increased spontaneous firing rates across a wide-frequency range, suggesting that they might also show increased sound-evoked responses and reduced latencies to higher-intensity sounds. However, no studies have examined bushy cells in relationship to hyperacusis. Herein, we test the hypothesis that bushy cells may contribute to the neural basis of hyperacusis by employing noise-overexposure and single-unit electrophysiology. We find that bushy cells exhibit hyperacusis-like neural firing patterns, which are comprised of enhanced sound-driven firing rates, reduced first-spike latencies and wideband increases in excitability.

Indexed as

AnimalsCochlear NerveCochlear NucleusEvoked Potentials, AuditoryFemaleGuinea PigsHyperacusisLoudness PerceptionNoiseTinnitus

Identifiers

PMID33244141
PMCPMC7693270
OpenAlexW3109075032

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.