Abstract

Air-conducted sound and bone-conduced vibration activate otolithic receptors and afferent neurons in both the utricular and saccular maculae, and trigger small electromyographic (EMG) responses [called vestibular-evoked myogenic potentials (VEMPs)] in various muscle groups throughout the body. The use of these VEMPs for clinical assessment of human otolithic function is built on the following logical steps: (1) that high-frequency sound and vibration at clinically effective stimulus levels activate otolithic receptors and afferents, rather than semicircular canal afferents, (2) that there is differential anatomical projection of otolith afferents to eye muscles and neck muscles, and (3) that isolated stimulation of the utricular macula induces short latency responses in eye muscles, and that isolated stimulation of the saccular macula induces short latency responses in neck motoneurons. Evidence supports these logical steps, and so VEMPs are increasingly being used for clinical assessment of otolith function, even differential evaluation of utricular and saccular function. The proposal, originally put forward by Curthoys in 2010, is now accepted: that the ocular vestibular-evoked myogenic potential reflects predominantly contralateral utricular function and the cervical vestibular-evoked myogenic potential reflects predominantly ipsilateral saccular function. So VEMPs can provide differential tests of utricular and saccular function, not because of stimulus selectivity for either of the two maculae, but by measuring responses which are predominantly determined by the differential neural projection of utricular as opposed to saccular neural information to various muscle groups. The major question which this review addresses is how the otolithic sensory system, with such a high density otoconial layer, can be activated by individual cycles of sound and vibration and show such tight locking of the timing of action potentials of single primary otolithic afferents to a particular phase angle of the stimulus cycle even at frequencies far above 1,000 Hz. The new explanation is that it is due to the otoliths acting as seismometers at high frequencies and accelerometers at low frequencies. VEMPs are an otolith-dominated response, but in a particular clinical condition, semicircular canal dehiscence, semicircular canal receptors are also activated by sound and vibration, and act to enhance the otolith-dominated VEMP responses.

Highlights

  • Before the 1990s, the usual way to probe the function of the otoliths was to measure responses, such as eye movements or perception, to maintained or low-frequency linear acceleration stimuli provided by sleds or centrifuges or tilting chairs [3,4,5,6,7,8]

  • The primary question is: are vestibular-evoked myogenic potential (VEMP) responses to sound (ACS) or bone-conducted vibration (BCV) really due to vestibular activation, since obviously sound and vibration stimulate cochlear receptors? That question was answered by showing the presence of VEMPs in patients without hearing but with vestibular function, and the absence of VEMPs in patients with hearing but without vestibular function after systemic gentamicin [11, 13, 17]

  • The major question is how sound and vibration activate otolithic receptors and afferents, and that is the main focus of this review—the physiological basis for using these myogenic potentials to index otolith function, and the rationale for using these tests to test utricular or saccular function differentially

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Summary

Introduction

Before the 1990s, the usual way to probe the function of the otoliths was to measure responses, such as eye movements or perception, to maintained or low-frequency linear acceleration stimuli provided by sleds or centrifuges or tilting chairs [3,4,5,6,7,8]. This neural evidence of otolithic activation by high frequencies is the foundation on which VEMPs to ACS and BCV are used to test otolith function.

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