Anatomy and Physiology of the Auditory System
•Download as PPT, PDF•
23 likes•12,877 views
An introductory lecture to the anatomy and physiology of the auditory system.
Recommended
More Related Content
What's hot
What's hot (20)
Viewers also liked
Viewers also liked (20)
Similar to Anatomy and Physiology of the Auditory System
Similar to Anatomy and Physiology of the Auditory System (20)
More from Csilla Egri
More from Csilla Egri (9)
Recently uploaded
Recently uploaded (20)
Anatomy and Physiology of the Auditory System
- 1. The Auditory System Csilla Egri, KIN 306 Spring 2012 The system that allows you to hear the most annoying sound in the world
- 2. Outline Anatomy of the ear Sensory transduction Cochlea Organ of Corti Frequency tuning Auditory pathways Localization of sound Auditory disorders 2
- 3. Anatomy of the Ear 3 B&B Figure 13-6
- 4. Anatomy of the Ear: External Ear4 folds of pinna provide cues about vertical location of sound gathers and focuses sound energy on tympanic membrane
- 5. Anatomy of the Ear: Middle Ear 5 amplifies vibrations of tympanic membrane to oval window matches low acoustic impedance of air to high acoustic impedance of fluid of the inner ear Eustachian tube
- 6. Anatomy of the Ear: Inner Ear 6 connected to the middle ear via two openings: oval window (entrance) & round window (exit) contains the cochlea a coiled tube separated into three fluid filled partitions location of the Organ of Corti, the sensory organ responsible for sound transduction perilymph endolymph B&L Figure 8-17Eustachian tube Cochlea – partially unravelled Helicotrema or apex Perilymph ≈ CSF What is the composition of CSF compared to plasma?
- 7. Sensory Transduction: Overview7 1. Ossicles amplify sound wave from tympanic membrane to oval window 2. Creates pressure wave in cochlear fluid 3. Deforms basilar membrane causes round window to bulge out 4. Motion of basilar membrane is transduced into action potentials by hair cells in organ of Corti located along the basilar membrane
- 8. Cochlea: cross-section8 Reissner’s membrane separates scala media from scala vestibuli Basilar membrane separates scala media from scala tympani Tectorial membrane attached along one edge of the wall to scala media Organ of Corti Located in scala media on top of basilar membrane B&B Figure 13-9
- 9. Cochlea: Organ of Corti 9 contains hair cells with sterocilia embedded into the tectorial membrane outer hair cells: stereocilia are arranged in V-like structure in three parallel rows inner hair cells: stereocilia are arranged linearly in single row 90% of afferents synapse on inner hair cells As basilar membrane moves up/down with pressure waves, stereocilia of hair cells bend against tectorial membrane
- 10. Sensory Transduction: Hair cells10 Stereocilia coupled by “tip links” Upward displacement of basilar membrane bends stereocilia towards kinocillium Opens mechanically gated non- selective cation channels = depolarization Excitatory neurotransmitter released = AP in afferent nerve fibre Not all afferent fibres fire AP in response to particular sound frequency B&B Figure 13-15 Endolymph High [K+ ] Perilymph Low [K+ ] +80mV -60mV 0mV
- 11. Frequency Tuning of Basilar Membrane11 Due to geometry of basilar membrane Base: narrower & stiffer Vibrates at higher frequencies Apex: wider & more flexible Vibrates at lower frequencies Maximal firing of afferent fibers depends on location along basilar membrane Frequency tuning: tonotopic mapping of frequency in the basilar membrane and organ of Corti
- 12. Auditory Pathways 12 Cochlear afferents synapse on cochlear nuclei in the medulla on the same side Most second order neurons cross over and synapse in the superior olivary nucleus Receives input from both ears (binaural) Medial and lateral superior olive (MSO and LSO) important in computing location of sound
- 13. Auditory Pathways 13 Ascend via the lateral meniscus tract on ipsilateral side to the inferior colliculus in the midbrain Fourth order neurons travel to the medial geniculate nucleus (MGN) in the thalamus Terminate in the primary auditory cortex in the temporal lobe Tonotopic organization maintained from cochlear nuclei to auditory cortex
- 14. Sound Localization 14 two strategies to localize the horizontal position of sound sources, depending on the frequency frequencies above 3 kHz use interaural intensity differences computed by neural circuitry in the lateral superior olive (LSO) and the medial nucleus of the trapezoid body (MNTB) frequencies below 3 kHz use interaural time differences computed by neural circuitry in the medial superior olive (MSO) B&B Figure 14-15
- 15. Interaural Intensity Differences: LSO and MNTB15 cochlear nucleus on same side as location of sound directly excites LSO LSO excites inhibitory interneurons in contralateral MNTB Contralateral LSO inhibited Excitation/inhibition arrangement sends maximal signal to auditory cortex on same side as sound
- 16. Interaural Time Differences: MSO16 MSO neurons are coincident detectors: respond only when excitatory signals arrive simultaneously Anatomical differences in connectivity allow each MSO neuron to be sensitive to sound source from particular location
- 17. Auditory Cortex 17 Primary auditory cortex corresponds to Broadmann’s area _____ and ______ Sends projections to auditory association area Discrimination of sound patterns Wernicke’s area: language comprehension Lesion to this area results in receptive aphasia Wernicke’s area
- 18. Auditory Disorders 18 Sensorineural hearing loss Dysfunctions of the inner ear, vestibulocochlear nerve or auditory cortex Most common cause is damage to hair cells. Two examples include: Noise induced hearing loss Caused by auditory trauma or long term exposure to loud sounds Leads to structural damage or complete degeneration and loss of hair cells Sensory presbycusis Age related hearing loss Hair cell damage caused by factors other than auditory trauma Often occurs in both ears WebCT readings: Sensorineural Hearing Loss
- 19. Objectives After this lecture you should be able to: Describe the structure and function of the outer, middle, and inner ear Relate the anatomical organization of the cochlea and associated structures to sensory transduction of sound Explain how damage to these structures can cause hearing loss Differentiate between the mechanisms for localization of horizontal sound above and below 3kHz Outline the neuronal pathway from the cochlea to the auditory cortex 19
- 20. 20 1. What is the first location in the auditory pathway that receives input from both ears? 2. What does tonotopic organization mean? 3. Endolymph closely resembles the ionic composition of intra or extracellular fluid of a typical neuron? Test your knowledge
Editor's Notes
- Readings Boron & Boulpaep: Chapter 13, pages 343 - 346, 347 - 352 Berne & Levy: Chapter 8, pages 133 - 143 Image from: http://www.hhmi.org/bulletin/sept2005/features/popups/ear.html
- The auditory system is one of the engineering masterpieces of the human body. At the heart of the system is an array of miniature acoustical detectors packed into a space no larger than a pea. These detectors can faithfully transduce vibrations as small as the diameter of an atom, and they can respond a thousand times faster than visual photoreceptors. Such rapid auditory responses to acoustical cues facilitate the initial orientation of the head and body to novel stimuli, especially those that are not initially within the field of view. Although humans are highly visual creatures, much human communication is mediated by the auditory system; indeed, loss of hearing can be more socially debilitating than blindness. From a cultural perspective, the auditory system is essential not only to language, but also to music, one of the most aesthetically sophisticated forms of human expression. For these and other reasons, audition represents a fascinating and especially important aspect of sensation, and more generally of brain function.
- Because of arcing shape of pinna, reflected path of sound coming from above is shorter than that of sounds from below, therefore two sets of sounds arrive at different intervals in the ear. The first stage of the transformation of sound waves into neural signals occurs at the external and middle ears, which collect sound waves and amplify their pressure, so that the sound energy in the air can be successfully transmitted to the fluid-filled cochlea of the inner ear. Tympanic membrane = ear drum Resonant frequency means that sound energy near this frequency is boosted or amplified, which allows us to hear sound best at this frequency. Most human speech sounds are distributed in the bandwidth around 3 kHz. Most vocal communication occurs in the low-kHz range because transmission of airborne sound is less efficient at higher frequencies, and the detection of lower frequencies is difficult for animals the size of humans. Convolutions of pinna shaped to transmit more high-frequency components from elevated source than source at ear level. This effect can be demonstrated by recording sounds from different elevations after they have passed through an artificial external ear; when the recorded sounds are played back via earphones, so that the whole series is at the same elevation relative to the listener, the recordings from higher elevations are perceived as coming from positions higher in space than the recordings from lower elevations.
- The term “impedance” in this context describes a medium's resistance to movement. eustachian tube connects middle ear to nasopharaynx facilitates equalization of pressure on opposite sides of tympanic membrane Normally, when sound travels from a low-impedance medium like air to a much higher-impedance medium like water, almost all (more than 99.9%) of the acoustical energy is reflected. The middle ear overcomes this problem and ensures transmission of the sound energy across the air-fluid boundary by boosting the pressure measured at the tympanic membrane almost 200-fold by the time it reaches the inner ear. Two mechanical processes occur within the middle ear to achieve this large pressure gain. The first and major boost is achieved by focusing the force impinging on the relatively large-diameter tympanic membrane on to the much smaller-diameter oval window, the site where the bones of the middle ear contact the inner ear. A second and related process relies on the mechanical advantage gained by the lever action of the three small interconnected middle ear bones, or ossicles (i.e., the malleus, incus, and stapes), which connect the tympanic membrane to the oval window.
- Less protein than plasma with similar electrolyte composition (but more Cl-, less Ca2+ and K+) oval window opens to scala vestibuli and connects to space adjacent to oval window; scala tympani connects to round window scala vestibuli and scala tympani are filled with perilymph; scala media is filled with endolymph the cochlear partition does not extend all the way to the apical end of the cochlea, such that scala vestibuli and scala tympani connect through opening near the apex called the helicotrema as a result of this structural arrangement, inward movement of the oval window displaces the fluid of the inner ear, which causes the round window to bulge out slightly and deforms the basilar membrane
- as pressure wave travels through scala vestibuli it pushes down on scala media and causes basilar membrane to bow into scala tympani bowing of basilar membrane creates shear force relative to tectorial membrane causing it to tilt and bending tips of embedded stereocilia
- scala media is separated from scala vestibuli by Reissner’s membrane and from the scala tympani by the basilar membrane tectorial membrane is attached along one edge to wall of scala media Other wall is called stria vascularis
- Rods of corti help provide a rigid scaffold for hair cells and surrounding support cells in the organ of corti 90% of afferents receive input from inner hair cells, thus these are the most important for transduction of sound. Function of outer hair cells is less clear. There are efferent connections as well, which synapse on outer hair cells, perhaps helping tune the sterecoilia and adjust sensitivity to sound.
- Mechanotransduction in the hair cell. A, The hair bundle on the apical side of the cell has one large kinocilium, which is a true cilium with a 9 + 2 arrangement of microtubules, as well as 50 - 150 stereocilia, which contain actin and are similar to microvilli. Endolymph, which has a very high [K+], bathes the apical surface. Perilymph, with a much lower [K+], bathes the basolateral surface. Each cell contacts an afferent and efferent axon. B, At rest, a small amount of K+ leaks into the cells, driven by the negative membrane potential and high apical [K+]. Mechanical deformation of the hair bundle towards the kinocilium increases the opening of non-selective cation channels at the tips of the stereocilia, allowing K+ influx, depolarizing the cell, activating voltage-sensitive Ca++ channels on the basal membrane, causing release of synaptic vesicles, and stimulating the postsynaptic membrane of the accompanying sensory neuron. C, Mechanical deformation of the hair bundle away from the kinocilium causes the non-selective cation channels to close, leading to hyperpolarization and reduced transmitter release. D, The graph shows the relative conductance of a hair cell on the y axis, and the displacement of the hair bundle on the x axis. A displacement of only 0.5 μm, roughly the diameter of a single stereocilium, nearly saturates the conductance change. (D, Data from Crawford AC, Fettiplace R: Auditory nerve responses to imposed displacements of the turtle basilar membrane. Hearing Res 12:199-208, 1983.)the ionic composition of the endolymph is high in K+ ( 145mM) and low in Na+ (2mM) Downward deflection of basilar membrane results in hyperpolarization
- Tonotopy in the auditory system begins at the cochlea, the small snail-like structure in the inner ear that sends information about sound to the brain. Different regions of the basilar membrane in the organ of Corti, the sound-sensitive portion of the cochlea, vibrate at different sinusoidal frequencies due to variations in thickness and width along the length of the membrane. Nerves that transmit information from different regions of the basilar membrane therefore encode frequency tonotopically. Frequency tuning within the inner ear is attributable in part to the geometry of the basilar membrane, which is wider and more flexible at the apical end and narrower and stiffer at the basal end. One feature of such a system is that regardless of where energy is supplied to it, movement always begins at the stiff end (i.e., the base), and then propagates to the more flexible end (i.e., the apex). Apical end is 100x more compliant than basal end. Because the basilar membrane vibrates maximally at different positions for different frequencies of sound, it acts like mechanical frequency analyzer. Traveling waves along the cochlea. A traveling wave is shown at a given instant along the cochlea, which has been uncoiled for clarity. The graphs profile the amplitude of the traveling wave along the basilar membrane for different frequencies and show that the position where the traveling wave reaches its maximum amplitude varies directly with the frequency of stimulation. Georg von Békésy, working at Harvard University, showed that a membrane that varies systematically in its width and flexibility vibrates maximally at different positions as a function of the stimulus frequency. Using tubular models and human cochleas taken from cadavers, he found that an acoustical stimulus initiates a traveling wave of the same frequency in the cochlea, which propagates from the base toward the apex of the basilar membrane, growing in amplitude and slowing in velocity until a point of maximum displacement is reached. This point of maximal displacement is determined by the sound frequency. The points responding to high frequencies are at the base of the basilar membrane, and the points responding to low frequencies are at the apex, giving rise to a topographical mapping of frequency called TONOTOPY. Complex sounds made up of many frequencies produce similarly complex pattern of vibration along basilar membrane.
- Tonotopic organization: The spatial layout of frequencies in the cochlea along the basilar membrane is repeated in other auditory areas in the brain. This is called tonotopic organization. The primary auditory pathway begins with the auditory receptors in the cochlea. These synapse on spiking neurons in the spiral ganglia, the axons of which form the auditory (8th cranial) nerve. These then lead to the cochlear nucleus, then to the superior olive, then to the inferior colliculus, then to the medial geniculate nucleus, and finally on to auditory cortex. Crossing of the Fibers. Significant number of nerve fibers cross the brain and make connections with neurons on the side opposite from the side of the ear in which they begin. This happens very early on in the auditory system. Inter-aural comparisons are an important source of information for the auditory system about where a sound came from (see spatial localization below). The tonotopic organization of the cochlea is maintained in the three parts of the cochlear nucleus, each of which contains different populations of cells with quite different properties. In addition, the patterns of termination of the auditory nerve axons differ in density and type; thus, there are several opportunities at this level for transformation of the information from the hair cells. One set of pathways from the cochlear nucleus bypasses the superior olive and terminates in the nuclei of the lateral lemniscus on the contralateral side of the brainstem. These particular pathways respond to sound arriving at one ear only and are thus referred to as monaural. Some cells in the lateral lemniscus nuclei signal the onset of sound, regardless of its intensity or frequency. Other cells in the lateral lemniscus nuclei process other temporal aspects of sound, such as duration. The precise role of these pathways in processing temporal features of sound is not yet known. As with the outputs of the superior olivary nuclei, the pathways from the nuclei of the lateral lemniscus converge at the midbrain. The superior olive receives binaural inputs and is important for sound localization (discussed on next slides).
- Space is not mapped on the auditory receptor surface; thus the perception of auditory space must somehow be synthesized by circuitry in the lower brainstem and midbrain. Neurons within this auditory space map in the colliculus respond best to sounds originating in a specific region of space and thus have both a preferred elevation and a preferred horizontal location, or azimuth. Although comparable maps of auditory space have not yet been found in mammals, humans have a clear perception of both the elevational and azimuthal components of a sound's location, suggesting that we have a similar auditory space map. (Information is based on experiments in the barn owl, an extraordinarily proficient animal at localizing sounds.) Many neurons in the inferior colliculus respond only to frequency-modulated sounds, while others respond only to sounds of specific durations. Such sounds are typical components of biologically relevant sounds, such as those made by predators, or intraspecific communication sounds, which in humans include speech. The inferior colliculus is evidently the first stage in a system, continued in the auditory thalamus and cortex, that analyzes sounds that have particular significance
- Human voice frequency ranges from about 60Hz to 7 kHz. 20 Hz to about 20,000 Hz rangge of hearing Interaural: ear to ear difference Intensity simply means the loudness of the sound, the ear facing the sound hears it louder than the opposite ear because the head casts a sound shadow. At the cochlea, intensity coded for by the amplitude of the sound wave As amplitude increases: basilar membrane vibrates more strongly, hair cells release NTs at higher rates Stronger vibration of basilar membrane activates hair cells even in surrounding areas High threshold hair cells activated as well Low frequency sounds need to be detected via a different mechanism because the wavelenght of the sound is longer than the size of the head. Longer sound waves are diffracted around the head and differences in interaural intensity no longer occur. The delay in which the sound reaches each ear is used to compute the location,
- The head acts as an acoustical obstacle because the wavelengths of the sounds are too short to bend around it. Excitatory axons project directly from the ipsilateral anteroventral cochlear nucleus to the LSO (as well as to the MSO). Note that the LSO also receives inhibitory input from the contralateral ear, via an inhibitory neuron in the MNTB. This excitatory/inhibitory interaction results in a net excitation of the LSO on the same side of the body as the sound source. For sounds arising directly lateral to the listener, firing rates will be highest in the LSO on that side; in this circumstance, the excitation via the ipsilateral anteroventral cochlear nucleus will be maximal, and inhibition from the contralateral MNTB minimal. In contrast, sounds arising closer to the listener's midline will elicit lower firing rates in the ipsilateral LSO because of increased inhibition arising from the contralateral MNTB. For sounds arising at the midline, or from the other side, the increased inhibition arising from the MNTB is powerful enough to completely silence LSO activity. Note that each LSO only encodes sounds arising in the ipsilateral hemifield; it therefore takes both LSOs to represent the full range of horizontal positions. Lateral superior olive neurons encode sound location through interaural intensity differences. LSO neurons receive direct excitation from the ipsilateral cochlear nucleus; input from the contralateral cochlear nucleus is relayed via inhibitory interneurons in the MNTB. This arrangement of excitation-inhibition makes LSO neurons fire most strongly in response to sounds arising directly lateral to the listener on the same side as the LSO, because excitation from the ipsilateral input will be great and inhibition from the contralateral input will be small. In contrast, sounds arising from in front of the listener, or from the opposite side, will silence the LSO output, because excitation from the ipsilateral input will be minimal, but inhibition driven by the contralateral input will be great. Note that LSOs are paired and bilaterally symmetrical; each LSO only encodes the location of sounds arising on the same side of the body as its location.
- MSO cells work as coincidence detectors, responding when both excitatory signals arrive at the same time. For a coincidence mechanism to be useful in localizing sound, different neurons must be maximally sensitive to different interaural time delays. The axons that project from the anteroventral cochlear nucleus evidently vary systematically in length to create delay lines. (Remember that the length of an axon multiplied by its conduction velocity equals the conduction time.) These anatomical differences compensate for sounds arriving at slightly different times at the two ears, so that the resultant neural impulses arrive at a particular MSO neuron simultaneously, making each cell especially sensitive to sound sources in a particular place. Diagram illustrating how the MSO computes the location of a sound by interaural time differences. A given MSO neuron responds most strongly when the two inputs arrive simultaneously, as occurs when the contralateral and ipsilateral inputs precisely compensate (via their different lengths) for differences in the time of arrival of a sound at the two ears. The systematic (and inverse) variation in the delay lengths of the two inputs creates a map of sound location: In this model, E would be most sensitive to sounds located to the left, and A to sounds from the right; C would respond best to sounds coming from directly in front of the listener.
- The human auditory cortex. Broadmanns area 41, 42 Tonotopic: Of or being a structural arrangement, as in the auditory pathway, such that different tone frequencies are transmitted separately along specific parts of the structure. Frequency, pitch, direction, other? (noise vs. sound?) (A) Diagram showing the brain in left lateral view, including the depths of the lateral sulcus, where part of the auditory cortex occupying the superior temporal gyrus normally lies hidden. The primary auditory cortex (A1) is shown in blue; the surrounding belt areas of the auditory cortex are in red. (B) The primary auditory cortex has a tonotopic organization, as shown in this blowup diagram of a segment of A1.
- Both can get progressivley worse (impair ability to hear lower frequencies) both impair abilities to hear high frequency sounds
- Tonotopic: Of or being a structural arrangement, as in the auditory pathway, such that different tone frequencies are transmitted separately along specific parts of the structure.