3/6/2024 Physiology, Vestibular System - StatPearls - NCBI Bookshelf

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Physiology, Vestibular System

Authors

Jarett Casale1; Tivon Browne2; Ian V. Murray3; Gunjan Gupta4.

Affiliations
1 Campbell University School of Osteopathic Medicine
2 St George's University
3 Texas A&M University
4 IGMC

Last Update: May 1, 2023.

Introduction
The vestibular system is a complex set of structures and neural pathways that serves a wide variety of functions that
contribute to our sense of proprioception and equilibrium. These functions include the sensation of orientation and
acceleration of the head in any direction with associated compensation in eye movement and posture. These reflexes
are referred to as the vestibulo-ocular and vestibulospinal reflexes, respectively. The centrally located vestibular
system involves neural pathways in the brain that respond to afferent input from the peripheral vestibular system in
the inner ear and provide efferent signals that make these reflexes possible. Current data suggest that the vestibular
system also plays a role in consciousness, and dysfunctions of the system can cause cognitive deficits related to
spatial memory, learning, and navigation.[1][2][3]

Cellular Level
There are vast amounts of both afferent and efferent cellular connections involved in the vestibular system. Most of
the afferent nerve signals come from the peripheral vestibular system found in the inner ear within the petrous
temporal bone. The inner ear contains a bony labyrinth and a membranous labyrinth. The bony labyrinth is filled with
a fluid known as "perilymph" which is comparable to cerebrospinal fluid and drains into the subarachnoid space.
Suspended within the bony labyrinth is the membranous labyrinth that contains a fluid known as endolymph unique in
composition due to its high potassium ion concentration. Endolymph in the vestibular system is produced by the
Vestibular Dark Cells which are similar to the Stria vascularis of the cochlea. Endolymph within the membranous
labyrinth surrounds the sensory epithelium and interacts with hair cells within the vestibular apparatus providing the
high potassium gradient to facilitate depolarization of the hair cell and afferent nerve transmission. [4] The vestibular
apparatus comprises the utricle, saccule, and superior, posterior, and lateral semicircular ducts. The sensory
neuroepithelium in the utricle and saccule is the macula, and the sensory neuroepithelium in the semicircular ducts is
the crista ampullaris. Both neuroepithelial structures contain specialized mechanoreceptor cells called "hair cells."
Hair cells contain a vast number of cross-linked actin filaments called stereocilia that are connected at the tips by “tip
links.” The stereocilia contain cation channels at their apex and are organized in rows by length, with the tallest
stereocilium connected to an immobile kinocilium. The kinocilium, the only true cilium, is made of the characteristic
9 + 2 microtubule arrangement. [5][6] Hair cells are divided into Type 1 hair cells and Type 2 hair cells. Type 1 hair
cells have a high variability of resting discharge while Type 2 hair cells have a low variability of resting discharge.
Acceleration of endolymph results in the movement of stereocilia, leading to either depolarization or
hyperpolarization depending on the direction of the inertial drag. Movement towards the kinocilium causes the
interconnected tip links to pull open cation channels resulting in an influx of potassium ions and depolarization. The
depolarized hair cell releases glutamate to afferent nerve receptors and neurotransmission to the vestibular ganglion.
Movement in the opposite direction to the kinocilium causes stereocilia to converge resulting in tip links closing the
cation channels. Lack of potassium influx causes hyperpolarization of the hair cell and inhibition of glutamate release

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to the afferent nerve. [5][6][7] The vestibular ganglion, also known as Scarpa ganglion, contains thousands of bipolar
neurons that receive sensory input from hair cells within the macula and crista ampullaris. Afferent axons from the
vestibular ganglion join to become the vestibular nerve. The vestibular nerve then joins the cochlear nerve to become
cranial nerve VIII, the vestibulocochlear nerve. Afferent nerve signals carried by the vestibulocochlear nerve are then
interpreted by the central vestibular system within the brain. The central vestibular system unites the peripheral
signals from both ascending pathways to elicit eye, head, and body motor responses for control of balance and
orientation.[6]

Development
The development of the peripheral vestibular system begins with the formation of the otic placodes from surface
ectoderm in the third week. During the fourth week, the otic placodes become the otic pits when they become
surrounded by embryonic mesoderm. The otic pits then develop into the otic vesicles. The upper portion of the otic
vesicle becomes the vestibular apparatus. As the otic vesicle lengthens, a division occurs between the ventral saccular
portion and the dorsal utricular portion. The ventral saccular portion becomes the adult saccule and cochlear duct
while the dorsal utricular portion forms the utricle and semicircular canals. Ossification of the system begins at 19
weeks gestation and reaches adult size by 25 weeks except for the internal aperture of the vestibular aqueduct that
continues to develop until birth. Hair cells and otoconia develop at seven weeks with differentiation of Type 1 and
Type 2 hair cells occurring between 11 and 13 weeks.[8][9]

Function
The vestibular system functions to detect the position and movement of our head in space. This allows for the
coordination of eye movements, posture, and equilibrium. The vestibular apparatus found in the inner ear helps to
accomplish this task by sending afferent nerve signals from its individual components. The utricle and the saccule are
responsible for sensing linear acceleration, gravitational forces, and tilting of the head. The neuroepithelium found in
the utricle and saccule is the macula which provides neural feedback about horizontal motion from the utricle and
vertical motion from the saccule. Embedded within the otolithic membrane of the macula are small calcium carbonate
crystals known as otoliths that assist in hair cell response to the inertial drag of endolymph. Angular acceleration and
rotation of the head in various planes are sensed by the three semicircular ducts that are oriented at right angles to one
another. Each of the semicircular ducts contains a dilation near the opening to the utricle. This dilation is called the
ampulla which contains a neuroepithelial structure called the "crista ampullaris." The crista ampullaris is coated by a
gelatinous protein-polysaccharide substance known as the cupula which holds the hair cells in place. Unlike the
macula, the crista ampullaris does not contain otoliths. In addition to the functions associated with the peripheral
vestibular system, the central vestibular system allows for processing and interpretation of afferent signals and the
output of efferent signals. Efferent signals include the vestibulo-ocular reflex, which allows the eyes to remain fixed
on an object while the head is moving. This is accomplished by coordinating movement between both eyes involving
the parapontine reticular formation and output to various extraocular eye muscles involving the oculomotor and
abducens nerves. The vestibulospinal reflex maintains balance and posture through the coordination of spinal
musculature with head movement. Cognitive functions that involve the central vestibular system are based on
established neural pathways, although many pathways are still unknown. The known central vestibular connections
include the vestibulo-thalamo-cortical tract, dorsal tegmental nucleus to entorhinal cortex tract, and nucleus reticularis
pontis oralis to hippocampus tract. These tracts form a series of complex connections that play a functional role in
self-motion perception, spatial navigation, spatial memory, and object recognition memory.[3][2][6][1]

Mechanism
The mechanism involved with the function of the peripheral vestibular system involves the acceleration of endolymph
within the various structures of the vestibular apparatus. Head movement in various directions is responsible for this
acceleration that results in the stimulation of the stereocilia of hair cells. When the head stops accelerating, hair cells
return to their baseline position which allows them to respond to further changes in endolymph acceleration.
Depending on the direction of acceleration, the inertial drag of the endolymph will push the stereocilia either towards
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or away from the fixed kinocilium. Movement towards the kinocilium causes tip links to pull open cation channels
resulting in depolarization of the hair cell via potassium ion influx. Movement away from the kinocilium results in
closure of the cation channels and hyperpolarization and reduction in afferent firing rates. Depolarization results in the
opening of calcium channels. Calcium channel opening results in neurotransmitter release across the synaptic cleft,
leading to nerve transmission to the vestibular ganglion. Nerve signals pass through the 20,000 bipolar neurons in the
vestibular ganglion and leave along the vestibular nerve. The vestibular nerve joins the cochlear nerve and enters the
brainstem at the pontomedullary junction. The primary processor of vestibular signals is the vestibular nucleus
complex that extends from the rostral medulla to the caudal pons. Many signals are sent from the vestibular nucleus to
either the thalamus, cortex, or cerebellum that help to process and adjust efferent signals to postural or ocular muscles.
Of note, the hippocampus plays an important role in spatial memory, including the functions of navigation and
orientation.[6][1][7]

Related Testing
Many tests can help determine if the vestibular system is functioning properly. The oculocephalic reflex is a simple
test used to determine if the brainstem of a comatose patient is intact using the reflexes of the vestibular system. The
test involves rotating a patient’s head horizontally, which should activate the vestibular system on the ipsilateral side
of rotation. This results in the patient’s eyes slowly deviating to the side opposite of head movement if the brainstem
is intact. If the brainstem is not intact, the eyes will follow the movement of the head to the ipsilateral side.

Caloric testing is a test that uses differences in temperature to diagnose damage to the acoustic nerve. A small amount
of cold water or air is gently delivered into one of your ears. Your eyes should show an involuntary movement called
nystagmus. Then they should turn away from that ear and slowly back. If water is used, it is allowed to drain out of
the ear canal. Next, a small amount of warm water or air is gently delivered into the same ear. Again, your eyes
should show nystagmus. Then they should turn toward that ear and slowly back. [10]

More specific tests for components of vestibular function includes videonystagometry, the most common vestibular
function test. The test is divided into three parts including ocular motor, positional testing, and caloric testing. Other
diagnostic modalities include rotation tests and video head impulse testing (VHIT). Both of these tests use devices to
monitor eye movements when the head is rotated in various directions to test the integrity of the vestibulo-ocular
reflex.[3][11]

Clinical Significance
Dysfunction of the vestibular system can manifest symptomatically as vertigo, nausea, vomiting, visual disturbance,
hearing changes, and various cognitive deficits. The relationship of the vestibular system to cognition is not well
understood, but many patients with vestibular dysfunction exhibit impairment of spatial navigation, learning, memory,
and object recognition. The pathophysiology of vertigo can be defined as peripheral or central. Peripheral vertigo is
more common than central vertigo, and three of the most common etiologies include benign paroxysmal positional
vertigo, Meniere disease, and viral labyrinthitis.

Benign paroxysmal positional vertigo (BPPV) is the most common cause of peripheral vertigo and lasts for seconds to
minutes. Most cases are idiopathic but the pathophysiology is believed to be due to displaced otoconia in the posterior
semicircular canal that causes an inappropriate sensation of movement. BPPV is diagnosed based on a thorough
history and use of the Dix-Hallpike test with associated reproduction of vertigo symptoms and nystagmus. There are
many movement techniques used to treat BPPV; however, the Epley maneuver is often cited as being one of the most
effective. The technique involves rotating and tilting the head and body in various ways to reposition displaced
otoconia in the inner ear. For acute, severe exacerbations of BPPV, anti-vertigo medications are indicated to help with
symptom control.

Meniere disease is another cause of peripheral vertigo that can last for hours and also manifest with symptoms of
hearing loss and tinnitus. The pathophysiology of Meniere disease is the expansion of endolymph volume within the
membranous labyrinth. This volume expansion impacts both the vestibular apparatus and cochlea that are both filled

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with endolymph. Expansion of endolymph within the cochlear duct results in defects in hearing that differentiate it
from BPPV. Meniere disease is diagnosed based on clinical criteria, and currently, no curative treatments exist.
Symptoms are managed with anti-vertigo medications, low-salt diet, and surgical decompression of the
endolymphatic sac as a last option.

Viral labyrinthitis, also known as "vestibular neuritis," is another cause of peripheral vertigo that can be attributed to
inflammation of the vestibular nerve, secondary to a viral infection. Symptoms include a simultaneous loss of hearing
and balance function in the affected ear that can last from days to weeks. Treatment involves symptom control with
anti-vertigo medications, and symptoms will typically resolve in one to three weeks. In addition to the pathologies
listed, vestibular function in the elderly has been well studied as a contributing factor to dizziness and imbalance
leading to falls. This is due to the significant loss of both Type 1 and Type 2 hair cells that occurs most prominently
between the ages of 65 and 70.[3][12][7][13]

Salicylate (aspirin) can reversibly eliminate outer hair cell electromotility to induce hearing loss. Salicylate
competitively binds to the motor protein reversibly inhibiting electromotility. Other symptoms of aspirin toxicity
include nausea, vomiting, tinnitus, hyperpnea, and disorientation. Other common ototoxic agents include
aminoglycosides, furosemide, cisplatin, and quinines.[14]

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Disclosure: Jarett Casale declares no relevant financial relationships with ineligible companies.

Disclosure: Tivon Browne declares no relevant financial relationships with ineligible companies.

Disclosure: Ian Murray declares no relevant financial relationships with ineligible companies.

Disclosure: Gunjan Gupta declares no relevant financial relationships with ineligible companies.

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