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PMID: 18355969 Published · ppublish English Comparative Study Journal Article Research Support, N.I.H., Extramural

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

Neuroscience ·Vol. 153 ·No. 1 ·2008-04-22 ·Pages 289-99

Zhao X, Jones SM, Yamoah EN, Lundberg YW

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.

MeSH Terms
Adaptation, Physiological/genetics,physiology Animals Calcium-Binding Proteins Evoked Potentials/physiology Extracellular Matrix Proteins/genetics Mice Mice, Inbred C57BL Mice, Knockout Mice, Mutant Strains Otolithic Membrane/abnormalities,physiopathology,ultrastructure Postural Balance/physiology Vestibular Diseases/genetics,pathology,physiopathology Vestibule, Labyrinth/abnormalities,physiopathology,ultrastructure
Chemicals
Calcium-Binding Proteins Extracellular Matrix Proteins Oc90 protein, mouse
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Zhao X
Genetics Department, Boys Town National Research Hospital, 555 North 30th Street, Omaha, NE 68131, USA.
Jones S M
Yamoah E N
Lundberg Y Wang
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Article Info
Journal
Neuroscience
Abbr.
Neuroscience
ISSN
0306-4522
Published
2008-04-22
Epub
2008-00-10
Pages
289-99
Language
English
Region
United States
NLM ID
7605074
PMCID
PMC2567131
Subset
IM
Grants
NIDCD NIH HHS · R01 DC003826 · United States
NIDCD NIH HHS · R01 DC006443 · United States
NIDCD NIH HHS · R01 DC006443-03 · United States
NCRR NIH HHS · P20 RR018788-030004 · United States
NCRR NIH HHS · 1P20RR018788 · United States
NIDCD NIH HHS · DC008603 · United States
NIDCD NIH HHS · DC003826 · United States
NIDCD NIH HHS · DC007592 · United States
NIDCD NIH HHS · R01 DC007592 · United States
NIDCD NIH HHS · DC006443 · United States
NIDCD NIH HHS · R01 DC008603 · United States
NCRR NIH HHS · P20 RR018788 · United States
NIDCD NIH HHS · R01 DC008603-01A1 · United States
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