This powerpoint elaborates the mechanism of balance & anatomy of vestibular apparutus. It also depicts the anatomy & physiology of haircells in detail. I also explained the vestibular function tests used for diagnosis of various vestibular disorders.
2. Introduction
The main function of the mammalian vestibular system
is to
Provide general orientation of the body with respect to gravity
Enable balanced locomotion and body position
Readjust autonomic functions after body reorientation
Ensure gaze stabilization.
4. Physiology of equilibrium
Balance of body during static or dynamic positions is
maintained by 4 organs:
1. Vestibular apparatus
2. Eye
3. Posterior column of spinal cord
4. Cerebellum
8. Motion Decomposition
Every motion in space can be broken
down into
3 Rotational
degrees of freedom – 1. Yaw
(SCC) 2. Pitch
3. Roll
3 Translational
degrees of freedom – 1. Left–Right
(U & S) 2. Up–Down
3. For–Aft
9. Physiology of head movement
HEAD MOVEMENT SEMICIRCULAR CANAL
STIMULATED
YAW LATERAL
PITCH POSTERIOR + SUPERIOR
ROLL SUPERIOR + POSTERIOR
10. Cristae
Location – Ampullated ends of 3
SCC.
Elevated sensory area containing
sensory hair cells
Tips of cilia are embedded in a
gelatinous mass composed of
polysaccharide called – CUPULA
Cupula functions as a water tight
partition & displacement occurs in
one direction at a time as a swing
door.
11. Macula
Located in utricle – floor (horizontal)
& saccule – posterior wall (vertical)
The hair cells are embedded in a gelatinous
layer impregnated with crystals of CaCO3
called OTOLITH MEMBRANE.
A filamentous network connects the lower
surface of otolithic membrane with sensory
epithelium called SUBCUPULAR
MESHWORK .
A virtual curved line called STRIOLA
divides utricular hair cells into medial &
lateral groups
& sacuular hair cells into ventral & dorsal
groups with opposite orientation
12. Vestibular Sensory Cells
Vestibular sensory epithelium consists of 2 types
of hair cells –
TYPE 1 – Flask shaped sorrounded by cup shaped
thick myelinated single afferent nerve terminal
TYPE 2 – Cylindrical with multiple thin afferent
nerve terminals at its base
The apex of hair cells is bathed in endolymph
and is sorrounded by nonsensory supporting
cells & dark cells.
13. Hair Cells
Hair cell consists of a hair bundle
at the apical end.
Each HAIR BUNDLE consists
of 1 large knobed
KINOCILLIUM & 20 - 300
STEREOCILLIA
14. Stereocillia
Have a cytoskeleton made up of actin
filament crosslinked by fibrin
Arranged in a HEXAGONAL
configuration
With shortest steriocillia at one end &
tallest at other end like a staircase.
The ion channel involved in
mechanoelectrical transduction are
located in steriocillia.
Connected to each other by fibrillary
strands called TIP LINKS
The upper end of each tip link is anchored
to the stereocilium at a point called
INSERTIONAL PLATE or PLAQUE.
Tension in the tip link controls the
opening or closing of the ion channels.
15. Kinocillium
It is a true cillium consisting of an axoneme (9+2).
Only function of kinocillium is - transmission of stimulus forces
to stereocillia.
Displacement of stereocillia towards kinocillium causes
depolarization.
18. Gating Compliance
An intrinsic property of direct mechano-
electrical transduction that enhances hair
cell sensitivity.
Hair bundle displacement in the positive
direction opens transduction channels.
Channel opening decreases the stiffness of
the hair bundle
This in turn promotes further movement
in a positive direction resulting in a
positive feedback mechanism
19. Adaptation
It prevents saturation of mechano-transductor response from large
sustained stimuli > 25ms.
It also allows a cell to detect small stimuli in the presence of an
enormous background input.
2 distinct models of adaptation –
Active Motor Model
Calcium Dependent Closure Model
20. Active Motor Model Myosin 1b
Hair bundle deflection towards kinocilium
increases tension in tip links with opening of
transduction channels
DEPOLARIZATION
Motor cannot resist the increased tension
& slips down the stereocillium
Tip link tension reduced & channels closed
HYPERPOLARIZATION
Stereocillia returns to resting stage
21. Calcium Dependent Closure Model
Opening of
transduction
channel
Calcium enters &
binds to channel
protein
Closure of channel
22. Vestibulo-Ocular Reflex
• It is a reflex eye movement due to stimulation of cristae of SCC during head
rotation
• It helps in Gaze Stabilization by producing eye movements in the direction
opposite to head movement, thus preserving the image on the fovea.
• Movement of head to left left horizontal canal stimulated & right
horizontal canal inhibited
• To keep eyes fixed on a stationary point, both eyes move to right side by
stimulating right lateral rectus & left medial rectus muscles.
23. Principle Of VOR Generation (PUSH- PULL)
HEAD ROTATION TO LEFT
STIMULATES LEFT HORZ. CANAL
SIGNAL GOES TO MVN
AXONS DECUSSATE TO
CONTRALATERAL ABDUCENS
NUCLEUS
RT. LATR. RECTUS CONTRACTION
INTERNEURONS FROM RT. ABDUCENS
NUCLEUS AGAIN CROSSES TO LEFT BY
MLF & PROJECTS TO LEFT
OCCULOMOTOR NUCLEUS
LEFT MEDIAL RECTUS
CONTRACTION
HYPERPOLARIZATION OF
RIGHT SCC
RELAXATION OF LEFT
LATERAL RECTUS & RIGHT
MEDIAL RECTUS
PUSH
PULL
Right
24. Vestibulospinal reflex
Effector organs - Extensor muscles of neck, trunk, arms and
limbs.
The driving input here is mainly Gravity detected by the otolith
system.
These reflexes are mediated through projections of the vestibular
nuclei on to the Medial and Lateral Vestibulospinal tract.
Similar to the VOR, the same push–pull mechanisms are used for
controlling the balance between extensor and flexor muscles.
25. Cervicoocular reflex
When the head is fixed but the body is rotated, nystagmus may
be observed.
This reflex is based on the stimulation of neck receptors.
In humans, this reflex is very unreliable and unpredictable
Only in subjects with congenital peripheral vestibular loss, does
this alternative strategy for gaze stabilization become helpful.
26. Central Projections Of Vestibular System
In the brain stem there are 4 vestibular nuclei
Superior
Lateral
Medial
Descending
From there several projections are found to
Occulomotor Nuclei
Lateral & Medial Vestibulospinal Tract
Parapontine Reticular Formation
Vestibulocerebellum- Floculus, Nodulus
Nucleus Tractus Solitarius
Cingulate Gyrus
28. Vestibular Function Tests
Assessment of vestibular function can be divided
into 2 groups –
1. CLINICAL TESTS
2. LABORATORY TESTS
29. Clinical Tests Of Vestibular Function
1. Clinical examination of eye movements
2. Fistula Test
3. Romberg Test
4. Gait
5. Tests Of Cerebellar Dysfunction
30. Clinical Examination of Eye Movements
The oculomotor examination should include:
Nystagmus
Convergence;
Smooth pursuit;
Saccades;
Vestibulo-ocular reflexes;
Positional manoeuvres.
31. Nystagmus
It is defined as involuntary rhythmic oscillatory movement of
eyes.
Described under headings –
1. Plane – Horizontal, Vertical, Torsional
2. Waveform – Saw tooth / Jerk – Contains a fast &
slow phase
Pendular- Quasisinusoidal
No fast or slow phase
3. Direction – Indicated by direction of fast component
4. Intensity – ALEXANDERS LAW
1st degree – Nystagmus present when looks in
direction of fast component.
2nd degree - Nystagmus present when looks
straight ahead.
3rd degree – Nystagmus present when looks in
direction of slow component.
32. Types of Nystagmus
DIFFERENCE
Peripheral Central
Latency 2-20 s No latency
Duration < 1 min > 1 min
Direction Direction fixed Direction changing
Fatiguability Fatiguable Non fatiguable
Symptoms Severe Vertigo None
Suppressed by Visual fixation None
Enhanced by Darkness or by using
Frenzel’s glasses
None
Vestibular nystagmus is of 2 types
Peripheral - Due to lesions of Labyrinth or VIIIth Nerve.
Central – Due to lesions of Vestibular Nuclei, Brain stem, Cerebellum.
33. Central Nystagmus
Type of Nystagmus Cause Remarks
Pendular Nystagmus Multiple Sclerosis Can be disconjugate – vertical
in one eye & horizontal in other
eye.
Purely Torsional Syringomyelia
Vertical Downbeat Arnold Chiari Malformation
Vertical Upbeat Pontomedullary juncn. lesions
Congenital Nystagmus Jerk Nystagmus with slow
phase velocity exponentially
increasing.
Seasaw Nystagmus Mid-brain lesions One eye goes up other goes
down
Dissociated Nystagmus Internuclear Opthalmoplegia Only abducting eye shows
nystagmus
Periodic Alternating
Nystagmus
Lesions in Nodulus of
Cerebellum
Changes direction every 2
minutes
Perverted Nystagmus Multiple Sclerosis Nystagmus occuring in a a
plane other than that of
vestibular stimulation.
34. Vestibulo-Occular Reflex
VOR stabilizes gaze in space during head movements
By generating slow phase eye movements of an equal velocity but in
opposite direction to head movement.
Clinical Tests for VOR are –
1. Doll’s Head Manoeuvre
2. Dynamic Visual Acuity
3. Head Impulse Test
35. Doll’s Head Manoeuvre
Examiner oscillates the patients head from side
to side at a frequency of approx. 0.5-1Hz.
Maintain fixation
(Normal VOR)
Interrupted Eye movements with catch up
saccades towards fixation target
(Abnormal VOR)
Post Meningitis / Ototoxicity
Patient sits in front of examiner &
fixates a part of examiners face(nose)
36. Dynamic Visual Acuity
Patient reads a visual acuity chart
6/6
Standing behind the patient
Examiner oscillates the patient’s head
at approx. 1Hz. While a new visual
acuity is taken
Gross reduction of VOR
Deterioration of Two linesNo change in Visual Acuity
NORMAL
37. Head Impulse Test
Patient seats in front of Examiner
& fixate a target across the room
Head is turned briskly by 15 degree
across midline by the examiner
Fixation maintained
NORMAL
Acute Vestibular Neuronitis
Eyes moves with head &
refixate with catch up saccades.
38. Positional Manoeuvre (Hallpike)
Patient sits on a couch & looks straight ahead
at one point on the examiner’s face
Examiner holds the patient head & turns it 450 to right
Patient placed in supine position with head
hangs 300 below horizontal
Patient eyes are observed for nystagmus for minimum 20 sec
Nystagmus appearing after a latent period of 2-20 s
Last for < 1 min & is always in one direction
On subsequent repetitions nystagmus disappears
(Fatiguable)
Nystagmus appearing immediately,
changing direction & non fatiguable
BPPV
CENTRAL
LESIONS
39. Fistula test
Intermittent pressure on tragus induces nystagmus by pressure changes in
EAC which is transmitted to labyrinth.
Results - Negative Normal
Positive Erosion of Horz. SCC
Fenestration Operation
Post-Stapedectomy Fistula
Rupture of round window
False Negative Cholesteatoma covering the
fistula
Dead Labyrinth
False Positive Hypermobile stapes
(Congenital Syphilis)
Stapes connected to Utricular
macula by fibrous bands
(Meniere’s disease)
40. Romberg’s Test
Sways to the side of lesion
(Peripheral Lesion)
Shows instability
(Central Lesion)
No sway or instability
Sharpened Romberg’s Test
Pt. stands with one heel in
front of toes & arms folded
across the chest
Patient stands with feet
together & arms by the side
with eyes open then closed
41. Unterberger’s Test
Turns towards the
Hypoactive side
(Peripheral Lesion)
Shows instability
(Central Lesion)
Patient asked to walk on the spot with eyes
closed & keeping the arm & index fingers
pointing towards examiners index fingers
42. Gait
Sways to the side of lesion
(Peripheral Lesion)
Shows instability
(Central Lesion)
Paradoxical Improvement with
fast walking
Acute Vestibular Neuronitis
Patient is asked to walk along a straight line
to a fixed point, first with eyes open then
closed
43. Tests of Cerebellar Dysfunction
DISEASE OF SIGNS
CEREBELLAR HEMISPHERE Asynergia
Dysmetria
Adiadochokinesia
Rebound Phenomenon
MIDLINE OF CEREBELLUM Wide base Gait
Falling in any direction
Inability to make sudden turns while walking
Truncal ataxia
44. Laboratory Tests of Vestibular Function
Caloric Test
Modified Kobrak Test
Fitzgerald-Hallpike Test
Cold Air Caloric Test
Electronystagmography
Optokinetic Test
Rotation Test
Galvanic Test
Posturography
45. Caloric Test
Principle- Changes in temperature in Extn. Auditory canal induces
convection currents in endolymph of Lateral SCC causing vertigo &
nystagmus
Advantage – Only test available to test each labyrinth separately.
Disadvantage – Anatomic abnormality of Extn. Or Middle ear interfere with
results
Types – 3 types
1. Modified Kobrak Test
2. Fitzgerald-Hallpike Test
3. Cold Air Caloric Test
46. Modified Kobrak Test
Patient is seated with head tilted 600 backwards
(Horz. Canal in vertical position)
Ear irrigated with ice water for 60 sec
Start with 5ml NO RESPONSE
Nystagmus beating towards opposite ear 10 ml
NORMAL
20 ml
40 ml
DEAD
LABYRINTH
47. Fitzgerald- Hallpike Test
Patient lies supine with head tilted 300 forward
(Horz. Canal in vertical position)
Procedure follows order
LEFT COLD>>RIGHT COLD>>LEFTWARM>>RIGHT WARM
Gap of 5 minutes
Cold water induces nystagmus to opposite side
& warm water to same side of irrigation
Time taken from the start of irrigation to end of
nystagmus recorded in a chart called
CALORIGRAM
Irrigation for 4 min with
water at 200C
Ear is irrigated for 40 sec alternately with water at 300C &
440 C
NO RESPONSE
NO RESPONSE
DEAD LABYRINTH
48. Cold Air Caloric Test
It is done when there is Tympanic membrane
perforation.
Test is done with Dundas – Grant tube which
is a coiled copper tube wrapped in cloth.
Air in the tube is cooled by pouring ethyl
chloride & blown into ear
This is only a rough qualitative test.
49. Interpretations of Caloric Test
There are 3 main abnormalities of caloric response-
1. Bilateral Absence of Caloric Response
2. Unilateral Canal Paresis
3. Directional Preponderance
50. Bilateral Absence of Caloric Nystagmus
Occurs in –
Post- Meningitis
Ototoxic drugs
Meniere’s Disease
Head Trauma
Idiopathic
51. Unilateral Canal Paresis
It indicates a reduced or absent response from one ear.
Causes are –
Acoustic neuroma
Post labyrinthectomy
Vestibular nerve section
Can be expressed as percentage as
Response from Left ear =
L30 + L44 × 100
L30 + L44 + R30 + R44
52. Directional Preponderance
It indicates that the Duration of nystagmus to one side is 25-30%
more than other side irrespective of whether it is elicited from
right or left labyrinth.
DP occurs towards the side of central lesion &
away from the side of peripheral lesion
Right beating nystagmus =
L30 + R44
L30 + L44 + R30 + R44
× 100
53. Electro/Video nystagmography
It is a method of detecting & recording of
nystagmus.
It depends on the presence of
corneoretinal potentials recorded by
surface electrodes placed around orbit.
Advantage –
1. Detect fine nystagmus not visible to
naked eye
2. To keep a permanent record
3. To detect nystagmus in dark.
Disadvantage –
1. Cannot record torsional eye
movement
2. Other biological potentials can be
picked up as artifact (EEG)
54. Optokinetic test
Patient is asked to follow a series of
vertical stripes on a rotating drum.
Normally it produces nystagmus with
slow component in the direction of
moving stripes & fast component in
opposite direction.
Abnormality indicates central lesion.
55. Rotational Tests
Patient is seated in a Barany’s revolving
chair with head tilted 300 forward
rotated 10 turns in 20 s.
The chair is stopped abruptly &
nystagmus is observed towards the side
of rotation.
2 types of rotation-
Velocity Step/ Impulsive Rotation
Sinusoidal Rotation
Normally nystagmus lasts for 25-40s.
Advantage – Test can be performed in
cases of congenital abnormalities where
SCC failed to develop
Disadvantage- Both the labyrinths are
simutaneously stimulated.
56. Galvanic Test
Only test which differentiates an end organ lesion
from that of vestibular nerve.
Patient stands with his feet together eyes closed &
arms outstretched & then a current of 1mA is passed
to one ear.
Normally patient sways towards the side of anodal
current. (Intact vestibular nerve)
57. Posturography
It is a method to evaluate vestibular function by
measuring postural stability.
2 main types
Static Posturography- Fixed platform
Computerized Dynamic Posturography – Movable
platform