10. Sound Conduction and Transduction Flashcards

1
Q

What is sound?

A
  • Transverse wave
  • Consist of compressed and rarefied air
  • Characterised based on frequency/pitch
  • Loudness depends on the amplitude of the wave
  • Measured in decibels based on a logarithmic scale
  • The large range in sound intensities makes measuring sound difficult to manage, which is why we measure sound LEVELS (decibels)
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2
Q

Components of the outer ear

A
  1. The pinna= wing allows for the elevation of sound
  2. External auditory meatus- a cone at the proximal part of the canal which focuses the noise and increases the pressure at the tympanic membrane
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3
Q

Components of the middle ear

A
  1. The ossicles are the smallest bones in the body (MALLEUS, INCUS, STAPES)
  2. Air filled tympanic cavity
  3. Tympanic membrane- vibrates due to air waves, ossicles improve signal
  4. Fluid filled cochlea

The middle ear extends from the cochlea to the tympanic membrane

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4
Q

How are the pressure of vibrations increased at the tympanic membrane

A

Increas in pressure of vibrations is achieved by TWO methods:

  1. Focusing vibrations from the large surface area of the membrane to the smaller surface area of oval window
  2. The incus has a flexible joint with the stapes, the ossicles use leverage to increase the force of the oval winow
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5
Q

Action of the ossicles

A

The ossicles convert the movement of the tympanic membrane to the movement of the foot plate

(Trying to induce a pressure wave in the fluid of the cochlear)

The three ossicles transmit the vibration of the tympanic membrane onto the cochlea, which is a snail-shaped organ filled with liquid. Their role is to match the impedance and reduce the loss in energy as the vibration goes from the air to the cochlea.

The impedance measures of reluctance of a system in receiving energy from a source. The frequency at which the impedance of the system is minimal is called the resonant frequency.

Malleus and Incus are relics of evolution (reptilian jaw). Their position can be adjusted by the tensor tympanic muscle and stapedius muscles to control the tension of the tympanic membrane.

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6
Q

Why cant the tympanic membrane translate directly to the cochlear fluid?

A

99% of the energy of the sound wave would just bounce of the interface due to impedence- measures the reluctance of a system in recieving energy from a source

The frequency at which the impedence of a system is minimal is called the resonant frequency

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7
Q

TWO muscles that control the movements of the ossicles:

A
  1. Tensor Tympani
  2. Stapedius

counteract and reduce the movement of the ossicles as part of the AUDITORY REFLEX

i.e work when hearing a loud noise and when talking/ chewing so you dont hear internally generated noises

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8
Q

Hyperacusis

A

Painful sensitivity to low intensity sounds- can occur in conditions that lead to flaccid paralysis of auditory reflex muscles

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9
Q

How is the cochlea connected to the ossicles

A

Through the stapes

The stapes and the footplate vibrate the OVAL WINDOW- part of the membrane of the cochlea

The round window below this is a ‘pressure release’ window (round window moves out as pressure is placed on fluid to equalise it)

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10
Q

THREE compartments to the inner ear

A
  1. Scala Vestibuli (perilymph fluid)
  2. Scala Tympani (perilymph fluid)
  3. Scala Media (contains endolymph fluid)

The helicotrema connects the scalas vestibuli and tympani

It allows fluid mixing

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11
Q

Basilar membrane

A

The end destination of the conducted sound waves - The basilar membrane is an elastic structureof heterogenous mechanical properties that vibrates at different positions along its length in response to different frequencies.

Different parts of the basilar membrane are sensitive to different frequencies - this property is used to generate a place code or tonotopic map

The basilar membrane breaks complex sounds down by distributing the energy of each component frequency along its length. We need therefore sensory receptors along the whole length of the basilar membrane in order to detect all frequencies: these receptors are the hair cells

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12
Q

Organ of Corti

A

The sense organ of the cohlea of the inner ear which converts sound signals into nerve impulses that are transmitted to the brain via the cochlear nerve

Lies above the basilar membrane and beneath the tectorial membrane

Consists of inner hair cells and outer hair cells- snese deflection in the basilar membrane

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13
Q

Inner Hair cells function

A
  • Found on their own
  • Send connections back to the brain (afferents)
  • They have stereocilia which move in response to the movement of endolymph
  • Inner hair cells do not make contact with the tectorial membrane
  • 95% of the afferent projections (sensory axons that carry signals from the cochlea towards the brain) project from inner hair cells.
  • Inner hair cells provide sensory transductions
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14
Q

Outer hair cells funtion

A
  • Found in groups of THREE
  • These are in contact with the tectorial membrane
  • recieve efferent connections
  • They are Electromotile- they expand and contract
  • By expanding or contracting they can amplify the amount of vibration
  • Damage to the hair cells results in SENSORINEURAL hearing loss
  • Also responsible for otoacoustic emissions- noises the ear makes itself (could be cause of tinnitus)
  • Most of the efferent projections (from the brain to cochlea) connect to outer hair cells.
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15
Q

Formation of the auditory nerve

A

Via grouping of the outer and inner hair cells- cell bodies are found in the spiral ganglion

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16
Q

Hair cells mode of action

A

Just as is needed for all action potential generation the endolymph (where stercocilia are) and perilymph (where base is) have different ion concentrations (seperated by teh stria vascularis):

  • Endolymph- high K+/ low Na+
  • Perilymph- high Na+/ low K+

Simplified:

Upwards movement of the basilar membrane displaces the sterecilia towards the centre of the cochlea: K+ channels OPEN and the hair cell depolarises

Downwards movement of the BM displaces the stereocilia the other way: K+ channels CLOSE and there is hyperpolarisation

17
Q

Central auditory pathway

A

Fibres of the Organ of Corti project out of the cochlea via the auditory VESTIBULOCOCHLEAR nerve (C8)

at this level the projection is ipsilateral (after this point everything is BILATERAL i.e if you have a central defecit the problem will be on both sides)

This pathway then goes to the superior olivary nucleus

ALL the ascending pathwyas converge on the inferior colliculus which is involved in reflex associations e.g turning towards a loud noise

lateral inhibition also occurs in this pathway

18
Q

Location and component parts of the AUDITORY CORTEX

A

The primary auditory cortex (A1) is in the temporal lobe

It has some tonotopic organisation- like in the motor homunculus

Secondary auditory cortex- responds to ound coming on and off and the duration of the sound

19
Q

Response to short sound bursts (localisation)

A

Can use interaural time delay- the time difference between the sound reaching one ear and reaching the other

20
Q

Continuous tone localisation

A

In this case there is no start or end to the sound

Localisation therefore occurs through interaural intensity difference

will have a reduced intensity on the other side

21
Q

Causes of sensorineural deafness

A

1. Sensory

  • Presbyacusis (normal ageing)
  • Exposure to loud noise
  • Meniere’s disease
  • Toxicity i.e some antibiotics

2. Neural

  • Acoustic neuroma
  • viral infection

3. Central (rare)

  • Demethylation in MS
  • injury to central auditory pathway (lesions)

Sensorineural Hearing Loss = when the cochlea or the cochlear nerve is damaged, the signal transmitted to the auditory cortex is reduced or lost resulting in a sensorineural hearing loss. This is typically seen in acoustic schwannoma (tumour of the cochlear nerve) or cerebellar tumours expanding and pressing on the cochlear nerve

Conductive Hearing Loss = when diseases of the middle ear destroy the ossicles or stiffen their joints, the amplification system is eliminated resulting in conductive hearing loss. A heavily waxy ear can also block sound waves from the ear drum + fluid accumulation in children, abnormal growth of bone etc.

22
Q

What are the main causes of hearing loss?

A
  • Loud traumatic sounds: military, industrial, clubs
  • 200 genetic conditions that cause hearing problems
  • Infections like meningitis or congenital ones such as rubella or syphilis
  • Drugs: used for severe heart infections and chemotherapy
  • Ageing
23
Q

Define conductive hearing loss

A

when the ear is not capable of transmitting the vibration of sound waves onto the cochlea. Cerumen, infections such as otitis, tumors can all affect transmission

  • In children, fluid accumulation in the inner ear is a common cause of conductive hearing loss (cold, Ménière’s disease).
  • A perforated tympanic membrane is a form of conductive hearing loss.
  • An abnormal growth of bone (otosclerosis) can obstruct the ear canal.
  • Barotrauma is a temporary form of conductive hearing loss. (Valsalva maneuver to reopen the Eustachian tubes)
24
Q

How do the hair cells work as sensory receptors in the inner ear?

A
  • The motion of the basilar membrane deflects the hair bundles of the hair cells, that act as sensors.
  • The bending of stereocilia towards the tallest stereocilium (we can use a glass probe) changes the internal voltage of the cell, ultimately producing an electric signal that travels towards the brain. This is called Mechano-transduction (MT).
  • Stereocilia are connected by filamentous linkages called tip links. They work as small springs stretched by stereocilia’s sliding
  • The opening of MT ion channels in response to an external stimulus, relaxes the tip link and, in turn, the whole hair bundle.
  • Imagine pulling on a door, free to open, with an elastic string attached to the handle. As you pull, the stiffness of the string would appear to droponce the door opens.
  • Unlike a door, a healthy hair bundle actively complies with the direction of the stimulus: the measured stiffness becomes negative!
  • The hair bundle has the capacity to do work. This points to the existence of an active processin hair cells.
25
Q

Explain the active process of hair cells.

A

The need for an active amplification: large portion of energy is lost in the viscous damping effects of the cochlear liquids. The sensitivity and the sharp frequency selectivity of the cochlea cannot be explained solely by passive mechanical

properties: basilar membrane (BM) impedance. 4 aspects of the active process:

26
Q

Explain how electromobility works.

A

When the efferent fibres are activated, frequency selectivity and sensitivity is enhanced. The origin of the cochlear amplification and otoacoustic emissions might be the OHCs. Their cell body shortens and elongates when their internal voltage is changed. This is called electromobility and can happen at a rate of 80 kHz. It is due to the reorientation of the protein prestin.

The spontaneous back and forth movement might be the cause of otoacoustic emissions and possibly of other aspects of the active process. Caveat: otoacoustic emissions in animals without OHCs.

27
Q

Explain the use of cochlear implants.

A

Hearing loss is primarily due to the loss of hair cells. These do not regenerate in mammals.One solution is to bypass the dead cells and stimulate the nerve fibres directly: detect sounds, break them down into their constituent frequencies and send the signal directly to the auditory nerve via antennas.

An elongated coil is inserted into the cochlea with pairs of electrodes corresponding to single frequencies.

28
Q

Explain the transmission from hair cells to the brain.

A
  • Hair cells (mostly inner hair cells) form synapses with sensory neurons in the cochlear ganglion (spiral ganglion)
  • Neurotransmitters are continuously released at rest, but the rate changes in response to a change of the presynaptic voltage (as a result of MT ion channel gating).
  • Each ganglion cell responds best to stimulations at a particular frequency.
  • The tonotopic (sound-location) map begins.
29
Q

Explain the transmission from the spiral ganglion to the cochlear nuclei.

A
  • The axons in the cochlear nerve transmit the information to the the cochlear nucleus nucleus.
  • Each axon is responsive to a single frequency.
    • Some low threshold and high rate spontaneous activity, some high threshold but less spontaneous activity.
  • The firing pattern of a cochlear nerve encodes the periodicity of the stimulus.
30
Q

Explain the volley theory.

A

A population of nerve fibres can produce a phaselocked (a response is phase-locked once it happens at the same point of the cycle, every cycle) collective response even at frequencies that single nerve fibres could not manage individually.

It allows to encode middle and middle-high frequencies.

31
Q

Describe the cochlear nucleus

A

Nerve fibres convey information to the cochlear nucleus of the brain stem where different kinds of neurons are arranged tonotopically (low frequencies ventrally, high frequencies dorsally)

Neuronal cells in the cochlear nucleus and superior olive are heterogenous (in morphology and electrical properties) and have specialised roles in auditory processing.

Each perform a different operation: building blocks for more complex tasks

T-Stellate Cells - They encode sound frequency and intensity of narrowband stimuli. Their tonotropic array represent sounds’ spectra

Bushy Cells- Bushy cells produce more sharply but less temporally precise versions of the cochlear nerve fibres. They provide the resolution required to encode the relative time of arrival of inputs to the two ears

32
Q

Describe the superior olivary complex.

A

The superior olivary complex compares the bilateral activity of the cochlear nuclei.

Medial Superior Olive

  • Here the interaural time difference is computed: sounds are first detected at the nearest ear before they reach the other one
  • Bushy cells carry information about the timing of inputs at every cycle. A map of interaural delay can be formed due to delay lines.

Lateral Superior Olive

  • The LSO detects differences in intensity between the two ears (>2 kHz in humans due to head size). Neurons are excited by sounds arising from the ear in the same side (ipsilaterally), while they are inhibited by opposite sounds (contralaterally)
  • Interaural level difference is computed to localise sounds in the horizontal plane.

The Superior Olivary Complex neurons send feedback to the Hair Cells:

  • Neurons from the medial superior olive - IHCs bilaterally.
  • Neurons from the lateral superior olive - OHCs ipsilaterally.

The feedback is used to balance the responses from the two ears, but also to reduce the sensitivity of the cochlea.

33
Q

Describe the inferior colliculus

A
  • Here responses from different frequencies merge. In the IC all ascending pathways converge.
  • In mammals: central nucleus , dorsal cortex and external cortex. Only central nucleus is tonotopically organised.
  • The more we ascend towards the cortex the more neurons become responsive to complex sounds.
  • In the IC many carry information about sound location. Precedence effect
34
Q

Describe the superior colliculus

A
  • Here auditory and visual maps merge. Neurons are tuned to respond to stimuli with specific sound directions.
  • The auditory map here created is fundamental for reflexes in orienting the head and eyes to acoustic stimuli.
35
Q

Describe the auditory cortex

A
  • In the auditory cortex, neurons respond to complex sounds
  • Primary Auditory Cortex
    • The primary auditory cortex is located in the superior bank of the temporal lobe
    • This is the central area of the Auditory Cortex and it is tonotopically mapped
    • Loudness, rate and frequency modulation also seem to be mapped.
  • Superior Auditory Cortex
    • In the visual system, the outputs of the primary visual cortex are segregated.
    • We can identify a “what” and a “where” stream in the auditory system
    • In the visual system, this is clearly defined.