Evidence map›Paper›PMID 18355969›Full record

ArticleNeuroscience2008

Otoconin-90 deletion leads to imbalance but normal hearing: a comparison with other otoconia mutants.

X Zhao, S M Jones, E N Yamoah, Y Wang Lundberg

Open access · greenAbstract readComparative Study
In one paragraph

Article in Neuroscience, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
1.3field-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

35 citing papers in PubMed, 56 citations in OpenAlex.

  1. Article
  2. NADPH Oxidase 3: Beyond the Inner Ear.Antioxidants (Basel, Switzerland) · 2024
    Review
  3. Demyelination and NaeNeuro · 2024
    Article
  4. Article
  5. Advances in otolith-related protein research.Frontiers in neuroscience · 2022
    Review
  6. Review
  7. Functional cooperation between two otoconial proteins Oc90 and Nox3.Journal of vestibular research : equilibrium & orientation · 2021
    Article
  8. Characterization of the transcriptomes ofAmerican journal of stem cells · 2020
    Article
  9. Article
  10. Article
  11. cVEMP correlated with imbalance in a mouse model of vestibular disorder.Environmental health and preventive medicine · 2019
    Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. Spatiotemporal differences in otoconial gene expression.Genesis (New York, N.Y. : 2000) · 2016
    Article
  17. Article
  18. Article
  19. Article
  20. 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.

X ZhaoGenetics Department, Boys Town National Research Hospital, 555 North 30th Street, Omaha, NE 68131, USA.
S M Jones
E N Yamoah
Y Wang Lundberg
East Carolina University · USUniversity of California, Davis · US

Funding

TRANSGENIC EXPRESSION ANALYSIS OF MIRNA-144P20RR018788 · NCRR · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI SMITH, SHELLEY D · 2003 to 2011
$16.5M
Potassium Homeostasis in the Inner EarR01DC007592 · NIDCD · UNIVERSITY OF NEVADA RENO · PI YAMOAH, EBENEZER N · 2005 to 2014
$4.5M
PROPERTIES AND FUNCTIONS OF CA CHANNELS IN HAIR CELLSR01DC003826 · NIDCD · UNIVERSITY OF NEVADA RENO · PI YAMOAH, EBENEZER N · 2000 to 2014
$4.4M
OTOCONIA DEVELOPMENT AND MAINTENANCER01DC008603 · NIDCD · FATHER FLANAGAN'S BOYS' HOME · PI LUNDBERG, YUNXIA WANG · 2007 to 2011
$1.7M
Genetic basis for gravity receptor dysfunction in miceR01DC006443 · NIDCD · EAST CAROLINA UNIVERSITY · PI JONES, SHERRI M · 2006 to 2010
$1.6M
FUNCTIONAL PROPERTIES OF CA PUMPS IN HAIR CELLR01DC004215 · NIDCD · UNIVERSITY OF CINCINNATI · PI YAMOAH, EBENEZER N. · 1999 to 2003
$1.0M
NCRR NIH HHS 1P20RR018788NCRR NIH HHS P20 RR018788NIDCD NIH HHS DC003826NIDCD NIH HHS DC006443NIDCD NIH HHS DC007592NIDCD NIH HHS DC008603NIDCD NIH HHS R01 DC003826NIDCD NIH HHS R01 DC004215NIDCD NIH HHS R01 DC006443NIDCD NIH HHS R01 DC007592NIDCD NIH HHS R01 DC008603
6 · The paper itself

Abstract

Our sense of gravitation and linear acceleration is mediated by stimulation of vestibular hair cells through displacement of otoconia in the utricle and saccule (the gravity receptor organ). We recently showed that otoconin-90 (Oc90) deletion led to formation of giant otoconia. In the present study, we determined the extent to which the giant otoconia affected balance and gravity receptor sensory input and compared the findings with other otoconia mutants. We employed a wide spectrum of balance behavioral tests, including reaching and air-righting reflexes, gait, swimming, beam-crossing, rotorod latencies, and a direct measure of gravity receptor input, vestibular evoked potentials (VsEPs). All tests on homozygous adult mutants consistently ranked the order of imbalance as (from worst to best) Nox3(het)<otopetrin 1(tlt)<Oc90 null<Oc90 wild type and C57Bl/6 mice using systematic statistical comparisons of the frequency of occurrence or the severity of abnormal functions. This order coincides with the degree of otoconia deficiencies and is consistent with VsEP measures. Notably, all mice (except Nox3(het)) showed remarkable learned adaptation to peripheral vestibular deficits by staying on the rotating rod significantly longer in each successive trial, and the rate and extent of such learned improvements ranked the same order as their initial balance ability. Despite the vestibular morbidity, Oc90 null mice had normal hearing, as measured by auditory brainstem responses (ABRs) and distortion products of otoacoustic emissions (DPOAEs). The study demonstrates that the remnant otoconia mass in Oc90 nulls does stimulate the gravity receptor organs, which was likely responsible for the improved balance performance relative to strains with absent otoconia. Furthermore, the combination of direct electrophysiological measures and a series of behavioral tests can be used to interpret the imbalance severity arising from altered inputs from the gravity receptor end organ.

Indexed as

Adaptation, PhysiologicalAnimalsCalcium-Binding ProteinsEvoked PotentialsExtracellular Matrix ProteinsMiceMice, Inbred C57BLMice, KnockoutMice, Mutant StrainsOtolithic MembranePostural BalanceVestibular DiseasesVestibule, LabyrinthCalcium-Binding ProteinsExtracellular Matrix ProteinsOc90 protein, mouse

Identifiers

PMID18355969
PMCPMC2567131
OpenAlexW2001885448

What OpenQuestion holds

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Registered trials

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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.