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Middle ear muscle dysfunction as the cause of Meniere's disease

Bell, James Andrew

Description

The symptoms of Meniere’s disease form a distinct cluster: bouts of vertigo, fluctuating hearing loss, low-frequency tinnitus, and a feeling of pressure in the ear. Traditionally, these signature symptoms have pointed to some sort of pathology within the inner ear itself, but here the focus is shifted to the middle ear muscles. These muscles, the tensor tympani and the stapedius, have generally been seen as serving only a secondary protective role in hearing, but in this paper they are...[Show more]

dc.contributor.authorBell, James Andrew
dc.date.accessioned2017-10-26T01:09:14Z
dc.date.available2017-10-26T01:09:14Z
dc.identifier.issn2083-389X
dc.identifier.urihttp://hdl.handle.net/1885/132357
dc.description.abstractThe symptoms of Meniere’s disease form a distinct cluster: bouts of vertigo, fluctuating hearing loss, low-frequency tinnitus, and a feeling of pressure in the ear. Traditionally, these signature symptoms have pointed to some sort of pathology within the inner ear itself, but here the focus is shifted to the middle ear muscles. These muscles, the tensor tympani and the stapedius, have generally been seen as serving only a secondary protective role in hearing, but in this paper they are identified as vigilant gate-keepers – constantly monitoring acoustic input and dynamically adjusting hearing sensitivity so as to enhance external sounds and suppress internally generated ones. The case is made that this split-second adjustment is accomplished by regulation of inner ear pressure: when the middle ear muscles contract they push the stapes into the oval window and increase the pressure of fluids inside the otic capsule. In turn, hydraulic pressure squeezes hair cells, instantly adjusting their sensitivity. If the middle ear muscles should malfunction – such as from cramp, spasm, or dystonia – the resulting abnormal pressure will disrupt hair cells and produce Meniere’s symptoms. A wide-ranging review of Meniere’s disease and the middle ear muscles reinforces the link between the two. Since every striated muscle is prone to dystonia – an involuntary contraction involving derangement of its underlying control loop – middle ear muscle dystonia would lead to elevated pressure and abnormal hair cell function. The hypothesis is based on recognizing that the inner ear is a hydrostat – a cavity filled with fluid whose pressure is controlled by the middle ear muscles. Since the fluid is incompressible, even a slight contraction of the muscles can increase the pressure in the labyrinth to 3 kPa. The effect of such a pressure on the sensing cells within is crucial. Outer hair cells carry an internal turgor pressure of about 1 kPa, behaving physically like inflated balloons, and hence contraction of the middle ear muscles can instantly overcome internal cellular pressure, switch off ion channels, and reduce hearing sensitivity. This paper brings together supporting evidence and sets out major implications for Meniere’s disease, including possible treatments.
dc.format.mimetypeapplication/pdf
dc.publisherInstitute of Sensory Organs
dc.rights© Journal of Hearing Science
dc.rightsthe author confirmed it's an open access journal and he was a consulting editor of the journal.
dc.sourceJournal of Hearing Science
dc.source.urihttp://journalofhearingscience.websensa.com/media/attachments/2017/09/27/904674.pdf
dc.subjectauditory system
dc.subjectmiddle ear muscles
dc.subjectMeniere's disease
dc.subjectdystonia
dc.subjectintralabyrinthine pressure
dc.titleMiddle ear muscle dysfunction as the cause of Meniere's disease
dc.typeJournal article
local.description.notesthe author deposited 26/10/2017
local.identifier.citationvolume7
dcterms.dateAccepted2017-08
dc.date.issued2017-09
local.publisher.urlhttp://journalofhearingscience.websensa.com/
local.type.statusPublished Version
local.contributor.affiliationJohn Curtin School of Medical Research, Australian National University
local.bibliographicCitation.issue3
local.bibliographicCitation.startpage9
local.bibliographicCitation.lastpage25
local.identifier.doi10.17430/904674
dcterms.accessRightsOpen Access
dcterms.accessRightsOpen Access
CollectionsANU Research Publications

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