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Similarities and Differences Between Vestibular and Cochlear Systems – A Review of Clinical and Physiological Evidence

The evoked response to repeated brief stimuli, such as clicks or short tone bursts, is used for clinical evaluation of the function of both the auditory and vestibular systems. One auditory response is a neural potential — the Auditory Brainstem Response (ABR) — recorded by surface electrodes on the...

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Autores principales: Curthoys, Ian S., Grant, John Wally, Pastras, Christopher J., Fröhlich, Laura, Brown, Daniel J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8397526/
https://www.ncbi.nlm.nih.gov/pubmed/34456671
http://dx.doi.org/10.3389/fnins.2021.695179
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author Curthoys, Ian S.
Grant, John Wally
Pastras, Christopher J.
Fröhlich, Laura
Brown, Daniel J.
author_facet Curthoys, Ian S.
Grant, John Wally
Pastras, Christopher J.
Fröhlich, Laura
Brown, Daniel J.
author_sort Curthoys, Ian S.
collection PubMed
description The evoked response to repeated brief stimuli, such as clicks or short tone bursts, is used for clinical evaluation of the function of both the auditory and vestibular systems. One auditory response is a neural potential — the Auditory Brainstem Response (ABR) — recorded by surface electrodes on the head. The clinical analogue for testing the otolithic response to abrupt sounds and vibration is the myogenic potential recorded from tensed muscles — the vestibular evoked myogenic potential (VEMP). VEMPs have provided clinicians with a long sought-after tool — a simple, clinically realistic indicator of the function of each of the 4 otolithic sensory regions. We review the basic neural evidence for VEMPs and discuss the similarities and differences between otolithic and cochlear receptors and afferents. VEMPs are probably initiated by sound or vibration selectively activating afferent neurons with irregular resting discharge originating from the unique type I receptors at a specialized region of the otolithic maculae (the striola). We review how changes in VEMP responses indicate the functional state of peripheral vestibular function and the likely transduction mechanisms allowing otolithic receptors and afferents to trigger such very short latency responses. In section “ELECTROPHYSIOLOGY” we show how cochlear and vestibular receptors and afferents have many similar electrophysiological characteristics [e.g., both generate microphonics, summating potentials, and compound action potentials (the vestibular evoked potential, VsEP)]. Recent electrophysiological evidence shows that the hydrodynamic changes in the labyrinth caused by increased fluid volume (endolymphatic hydrops), change the responses of utricular receptors and afferents in a way which mimics the changes in vestibular function attributed to endolymphatic hydrops in human patients. In section “MECHANICS OF OTOLITHS IN VEMPS TESTING” we show how the major VEMP results (latency and frequency response) follow from modeling the physical characteristics of the macula (dimensions, stiffness etc.). In particular, the structure and mechanical operation of the utricular macula explains the very fast response of the type I receptors and irregular afferents which is the very basis of VEMPs and these structural changes of the macula in Menière’s Disease (MD) predict the upward shift of VEMP tuning in these patients.
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spelling pubmed-83975262021-08-28 Similarities and Differences Between Vestibular and Cochlear Systems – A Review of Clinical and Physiological Evidence Curthoys, Ian S. Grant, John Wally Pastras, Christopher J. Fröhlich, Laura Brown, Daniel J. Front Neurosci Neuroscience The evoked response to repeated brief stimuli, such as clicks or short tone bursts, is used for clinical evaluation of the function of both the auditory and vestibular systems. One auditory response is a neural potential — the Auditory Brainstem Response (ABR) — recorded by surface electrodes on the head. The clinical analogue for testing the otolithic response to abrupt sounds and vibration is the myogenic potential recorded from tensed muscles — the vestibular evoked myogenic potential (VEMP). VEMPs have provided clinicians with a long sought-after tool — a simple, clinically realistic indicator of the function of each of the 4 otolithic sensory regions. We review the basic neural evidence for VEMPs and discuss the similarities and differences between otolithic and cochlear receptors and afferents. VEMPs are probably initiated by sound or vibration selectively activating afferent neurons with irregular resting discharge originating from the unique type I receptors at a specialized region of the otolithic maculae (the striola). We review how changes in VEMP responses indicate the functional state of peripheral vestibular function and the likely transduction mechanisms allowing otolithic receptors and afferents to trigger such very short latency responses. In section “ELECTROPHYSIOLOGY” we show how cochlear and vestibular receptors and afferents have many similar electrophysiological characteristics [e.g., both generate microphonics, summating potentials, and compound action potentials (the vestibular evoked potential, VsEP)]. Recent electrophysiological evidence shows that the hydrodynamic changes in the labyrinth caused by increased fluid volume (endolymphatic hydrops), change the responses of utricular receptors and afferents in a way which mimics the changes in vestibular function attributed to endolymphatic hydrops in human patients. In section “MECHANICS OF OTOLITHS IN VEMPS TESTING” we show how the major VEMP results (latency and frequency response) follow from modeling the physical characteristics of the macula (dimensions, stiffness etc.). In particular, the structure and mechanical operation of the utricular macula explains the very fast response of the type I receptors and irregular afferents which is the very basis of VEMPs and these structural changes of the macula in Menière’s Disease (MD) predict the upward shift of VEMP tuning in these patients. Frontiers Media S.A. 2021-08-12 /pmc/articles/PMC8397526/ /pubmed/34456671 http://dx.doi.org/10.3389/fnins.2021.695179 Text en Copyright © 2021 Curthoys, Grant, Pastras, Fröhlich and Brown. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Curthoys, Ian S.
Grant, John Wally
Pastras, Christopher J.
Fröhlich, Laura
Brown, Daniel J.
Similarities and Differences Between Vestibular and Cochlear Systems – A Review of Clinical and Physiological Evidence
title Similarities and Differences Between Vestibular and Cochlear Systems – A Review of Clinical and Physiological Evidence
title_full Similarities and Differences Between Vestibular and Cochlear Systems – A Review of Clinical and Physiological Evidence
title_fullStr Similarities and Differences Between Vestibular and Cochlear Systems – A Review of Clinical and Physiological Evidence
title_full_unstemmed Similarities and Differences Between Vestibular and Cochlear Systems – A Review of Clinical and Physiological Evidence
title_short Similarities and Differences Between Vestibular and Cochlear Systems – A Review of Clinical and Physiological Evidence
title_sort similarities and differences between vestibular and cochlear systems – a review of clinical and physiological evidence
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8397526/
https://www.ncbi.nlm.nih.gov/pubmed/34456671
http://dx.doi.org/10.3389/fnins.2021.695179
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