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Chapter 31 Sensory Function of the Nervous System Part I Structure of the Ear Auditory Canal: conducts sound to the eardrum Tympanic membrane (Eardrum): thin membrane ... – PowerPoint PPT presentation

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Title: Sensory%20Function%20of%20the%20Nervous%20System


1
Chapter 31
  • Sensory Function of the Nervous System

2
Contents
  • Sensory receptors and sensory organs
  • Pain
  • The visual system
  • The Auditory Systems

3
Section 1Sensory Receptor and Sensory Organ
4
Part 1 Sensory Receptors
  • specialized nerve cells that transduce energy
    into neural signals
  • mode specific
  • Law of Specific Nerve Energies(????????)
    sensory messages are carried on separate channels
    to different areas of the brain
  • detect a small range of energy levels
  • Eye 400-700 nM
  • Ear 20-20,000 Hz
  • Taste buds specific chemicals

5
Spectrum of the Electromagnetic Wave
6
Somatic Sensory Nerve Endings
7
Free Nerve Endings
  • dendrites interspersed among other cells/tissues
  • pain, temperature, touch

8
Encapsulated Nerve Endings
  • dendrites with special supporting structures
  • mechanoreceptors and proprioceptors

9
Classification of Receptors Location
  • Exteroceptors
  • Located on the body surface or specialized to
    detect external stimuli
  • Pressure, pain, temp, touch, etc.
  • Visceroceptor
  • within internal organs, detect internal stimuli
  • Blood pressure, pain, fullness.
  • Proprioceptors
  • Limb and body position and movement.
  • in the joints and muscles
  • in the vestibular structures and the semicircular
    canals of the inner ear.

10
Classification of Receptors Modalities
  • Mechanoceptive
  • Detects stimuli which mechanically deform the
    receptor
  • Pressure, vibration, touch, sound.
  • Thermoceptive
  • Detects changes in temperature
  • hot/cold
  • Nociceptive (pain)
  • Detects damage to the structures
  • Photoreceptors
  • Detect light vision,
  • retinal of the eye
  • Chemoceptive
  • Detect chemical stimuli
  • CO2 and O2 in the blood, glucose, smell, taste

11
Classification of Receptors Complexity
  • Simple receptors
  • Usually a single modified dendrite
  • General sense
  • Touch, pressure, pain, vibration, temperature
  • Complexity
  • High modified dendrites, organized into complex
    structures
  • ear, eye.
  • Special senses
  • Vision, hearing, smell, taste

12
Which receptor?
13
Sequence of Events in a Receptor
Basic Function
Stimulus
Amplification
14
Part 2 Properties of the Receptors
  • Adequate Stimulus
  • Transduction
  • Adaptation
  • Encoding

15
1. Adequate Stimulus
  • The type of stimulus the receptor is highly
    sensitive
  • Receptor specially designed for one kind of
    stimulus
  • The lowest threshold
  • Insensitive to other stimulation

16
2. Transduction
  • A process by which an environmental stimulus
    becomes encoded as a sequence of nerve impulses
    in an afferent nerve fiber
  • Transduce sensory energy into neural
    (bioelectrical) energy
  • Receptor potentials Changes in the transmembrane
    potential of a receptor caused by the stimulus.
  • Generator Potential A receptor potential that is
    strong enough (reaches threshold) to generate an
    action potential
  • The stronger the sitmulus (above threshold) the
    more APs are fired over a given time period
  • translated by the CNS as a strong sensation

17
Receptor Potential and Generator Potential
18
3. Adaptation
The sensory receptor adapt to any constant
stimulus after a period of time Phasic receptors
quickly adapt. Most exteroceptors Tonic
receptors adapt slowly or not at all. Most
visceroceptors
19
Phasic and Tonic Receptors
  • Phasic Receptor
  • alert us to changes in sensory stimuli
  • cease paying attention to constant stimuli
  • Tonic Receptor
  • useful in situations requiring maintained
    information about a stimulus.

20
4. Encoding
  • The quality of the stimulus is encoded in the
    frequency of the action potentials.

21
Stretch Receptors Weak stretch causes low
impulse frequency on neuron leaving
receptor. Strong stretch causes high impulse
frequency on neuron leaving receptor.
Frequency Code
Membrane potential
Time
22
Summary
  • The external internal environments are
    monitored by sensory receptors.
  • Each type of receptor is excited most effectively
    by only one modality of stimulus known as the
    adequate stimulus.
  • The stimulus is converted into an electrical
    potential.
  • Stimuli are detected as either static or dynamic
    events.
  • The intensity duration of the stimulus is
    frequency coded as bursts of action potentials in
    the primary afferent nerve.

23
Section 2. Pain
24
  • Pain is an unpleasant sensory and emotional
    experience associated with actual or potential
    tissue damage or described in terms of such
    damage
  • International Association for the Study
    of Pain

25
Why feel pain?
  • Gives conscious awareness of tissue damage
  • Protection
  • Remove body from danger
  • Promote healing by preventing further damage
  • Avoid noxious stimuli
  • Elicits behavioural and emotional responses

26
1. Nociceptors
  • special receptors that respond only to noxious
    stimuli and generate nerve impulses which the
    brain interprets as "pain".

27
Nociopectors
  • Adequate Stimulation
  • Temperature
  • Mechanical damage
  • Chemicals (released from damaged tissue)
  • Bradykinin, serotonin, histamine, K, acids,
    acetylcholine, proteolytic enzymes can excite the
    chemical type of pain.
  • Prostaglandins and substance P enhance the
    sensitivity of pain endings but do not directly
    excite them.

28
  • Hyperalgesia
  • ?The skin, joints, or muscles that have already
    been damaged are unusually sensitive.
  • A light touch to a damaged area may elicit
    excruciating pain
  • Primary hyperalgesia occurs within the area of
    damaged tissue
  • Secondary hyperalgesia occurs within the tissues
    surrounding a damaged area

29
2. Localization of Pain
  • Superficial somatic pain arises from skin areas
  • Deep somatic pain arises from muscle, joints,
    tendons (??) fascia (??)
  • Visceral Pain arises from receptors in visceral
    organs

30
3. Fast and Slow Pain
  • Most pain sensation is a combination of the two
    types of message.
  • sharp pain conducted by the A fibres
  • dull pain conveyed along C fibres

31
  • Fast pain (acute)
  • occurs rapidly after stimuli (.1 second)
  • sharp pain like needle puncture or cut
  • not felt in deeper tissues
  • larger A nerve fibers
  • Slow pain (chronic)
  • begins more slowly increases in intensity
  • in both superficial and deeper tissues
  • smaller C nerve fibers

32
  • Impulses transmitted to spinal cord by
  • Myelinated Ad nerves fast pain (80 m/s)
  • Unmyelinated C nerves slow pain (0.4 m/s)

33
  • Impulses ascend to somatosensory cortex via
  • Spinothalamic pathway (fast pain)
  • Reticular formation (slow pain)

34
4. Notable Features of Visceral pain
  • Caused by
  • distension of hollow organs
  • ischemia
  • inflammation
  • localized mechanical trauma may be painless
  • Poorly localized
  • may be referred
  • Often accompanied by strong autonomic and/or
    somatic reflexes

35
Afferent innervation of the viscera.
  • anatomical separation
  • nociceptive innervation in sympathetic nerves
  • non-nociceptive predominantly in vagus
  • Many visceral afferents are specialized
    nociceptors,
  • small (Ad and C) fibers involved.
  • Large numbers of silent/sleeping nociceptors,
    awakened by inflammation.
  • Nociceptor sensitization (hyperalgesia) well
    developed

36
Referred pain
  • Pain originating from organs perceived as coming
    from skin
  • Site of pain may be distant from organ

37
Convergence theory of Referred pain
  • both visceral and somatic afferents converge on
    the same interneurons in the pain pathways.
  • Excitation of the somatic afferent fibers is the
    more usual source of afferent discharge
  • the location of visceral receptor activation was
    referred to the somatic source.
  • The perception is incorrect.

The convergence of nociceptor input from the
viscera and the skin.
38
5. Pain Gate Theory
  • Melzack Wall (1965)
  • A gate, where pain impulses can be gated
  • The synaptic junctions between the peripheral
    nociceptor fiber and the dorsal horn cells in the
    spinal cord are the sites of considerable
    plasticity.
  • A gate can stop pain signals arriving at the
    spinal cord from being passed to the brain
  • Reduced pain sensation
  • Natural pain relief (analgesia)

39
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How does pain gate work?
  • The gate spinal cord interneurons that release
    opioids.
  • The gate can be activated by
  • Simultaneous activity in other sensory (touch)
    neurons
  • Descending nerve fibers from brain

41
Applications of pain gate
  • Stimulation of touch fibres for pain relief
  • TENS (transcutaneous electrical nerve
    stimulation)
  • Acupuncture
  • Massage
  • Release of natural opioids
  • Hypnosis
  • Natural childbirth techniques

42
6. Pain Relief
  • Aspirin and ibuprofen (???) block formation of
    prostaglandins that stimulate nociceptors
  • Novocain (????) blocks conduction of nerve
    impulses along pain fibers
  • Morphine lessen the perception of pain in the
    brain.

43
Section 3
  • The Visual System

44
Part 1. Structure of the Eyeball
45
Part2 Focusing on the Retina
  • The images of objects in the environment are
    focused on the retina.

46
1. Principle of Optics
  • Light rays are bent (refracted) when they pass
    from one medium into a medium of a different
    density.
  • Parallel light rays striking a biconvex lens are
    refracted to a point (principal focus) behind the
    lens.
  • The principle focus is on a line passing through
    the centers of a curvature of the lens, at the
    principal focal distance.

47
Light rays from an object that strike a lens more
than 20 ft (6 m) away are considered to be
parallel. The rays from an object closer than 20
ft are diverging and are brought to a focus
farther back than the principal focus. Biconcave
lenses cause light rays to diverge.
48
2. Emmertropia
  • The refractive system of the human eye
  • cornea, aqueous humor, crystalline lens, and
    vitreous humor.
  • When light coming from an object is brought to a
    focus, an image is formed.
  • Emmertropia
  • parallel rays of light are focused to an image on
    the retina.
  • normal human eye

49
3. Accommodation
  • Emmertropia ciliary muscle relax during seeing
    object farther than 6 m.
  • objects closer than 6 m are brought to a focus
    behind the retina,
  • the objects appear blurred.
  • Problem solved by accommodation
  • near objects are brought to a sharp focus on the
    retina

50
(1) Accommodation of lens
  • Increase bulging (refraction) of lens
  • Via contraction of ciliary muscle, relaxes the
    suspensory ligaments (parasympathetic fibers)

51
Focusing
Muscles relaxed Lens less spherical Focus far
Muscles working Lens more spherical Focus near
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Near Point
  • The power of accommodation is limited
  • The nearest distance of the eye at which an
    object can seen distinctly
  • the visual accommodation is at a maximum
  • Decline in the amplitude of accommodation in
    human with advancing age

56
Diopter???
57
(2) Pupillary reflex
  • Reduces the amount of light entering the eye
  • Restricts the light to the central part of the
    lens for more accurate vision
  • Increase the depth of focus (??)
  • Decrease the spherical aberration and chromatic
    aberration

58
(3) Convergence of eyeballs
  • Viewing near object causes both eyes to move
    inward
  • Move the images on the corresponding position on
    the retina of the two eyes

59
4. Error of Refraction
  • Caused by
  • shape of eye
  • power of lens

60
Farsightedness
  • less common
  • eye too short and/or lens too weak
  • light focuses behind retinal
  • correct with convex lens to add power

61
FARSIGHTEDNESS (HYPEROPIA)
UNCORRECTED
CORRECTED
62
Nearsightedness
  • more common
  • eye is too long and/or lens is too powerful
  • light focuses in front of retina
  • correct with concave lens to reduce power

63
NEARSIGHTEDNESS (MYOPIA)
UNCORRECTED
CORRECTED
64
  • Astigmatism
  • abnormal curvature of the cornea
  • Light from vertical and horizontal direction do
    not focuses in the same point

65
Oldsightedness (Presbyopia)
  • The crystalline lens tends to harden and the
    capsule itself becomes less elastic with age
  • The near point of distinct vision moves further
    and further away from the eye with age.
  • The far point is normal
  • May be compensated by placing a converging lens
    in front of the eye.

66
The loss in power of accommodation is most
significant and dramatic between the ages of 40
and 50
67
Part 3 Function of the Retina
68
I. Rod system and cone system
  • rod system
  • rods and subsequent bipolar cells and ganglion
    cells
  • cone system
  • cones and subsequent bipolar cells and ganglion
    cells.

69
Distribution of the cones and rods on the retina.
70
Rods
  • located mainly in periphery of retina
  • responsible for night vision
  • detail not detected
  • see black, white, and gray (no color)
  • several rods share 1 bipolar and 1 ganglion cell
  • rod vision lacks detail, but see in low light

71
Cones
  • located mainly in fovea
  • work best in bright light
  • enable us to see fine detail
  • responsible for color vision
  • each cone has its own bipolar and ganglion cell
  • this allows us to see detail but bright light is
    needed

72
Cones see detail but require bright light Rods
see in low light but lack detail
73
Evidence of Two Photoreceptor System
  • the nocturnal and diurnal animals
  • nocturnal animals have a preponderance of rods
  • diurnal animals have a preponderance of cones
  • visual pigment
  • one classes (rhodopsin) in the rods
  • three classes in the cones

74
II Transduction of Light Energy by Rod Cell
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1. Photochemical Reaction and Metabolism of
Rhodopsin
Rhodopsin the visual pigment (light-sensitive
pigment). combination of a protein part,
scotopsin (opsin) a carotenoid pigment, 11-cis
retinal Rhodopsin cis form of the retinal bind
with scotopsin.
11-cis retinal
77
Retinal Light Sensitive Pigment11-cis-Retinal
- All-trans-Retinal
Light
Dark
all-trans retinal (straight chain form)
11-cis retinal (bent shape form)
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Converting the All-trans Retinal into 11-cis
Retinal
  • Occurs under the dark environment
  • Requires metabolic energy
  • Catalyzed by the retinal isomerase.
  • Under the dim light, the 11-cis and 11-trans keep
    dynamic balance

Light
Dark
80
11-cis retinal opsin
all-trans retinal opsin
rhodopsin
isomerase
All-trans retinal
11-cis retinal
opsin
opsin
81
Vitamin A and Retinal (???)
  • All-trans retinol is one form of vitamin A
  • Vitamin A is present both
  • in the cytoplasm of the rods
  • in the pigment layer of the retina
  • Vitamin A is always available to form new retinal
    when needed.
  • Severe vitamin A deficiency - Night blindness.

82
2. Receptor Potential of Rods Hyperpolarization
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III Color Vision
85
Photochemistry of Color Vision by Cones
  • Three kinds of proteins on the photopigments
  • Sensitive to three kinds of light
  • Trichromatic Theory

86
Visible spectrum 380-760 nm (nm is a billionth
of a meter)
87
Trichromatic Theory of Color Vision
  • Occurs at the receptor level
  • Each cone is coated by one of 3 photopigments
  • Short-wave (blue)
  • Medium-wave (green)
  • Long-wave (red)
  • Ratio of activated cones color differentiation

88
Color Sensitivity of Different Cones
89
Primary Colors
  • Red, Green and Blue
  • can be mixed to produce any other color

90
Color Blindness
  • Sex-linked conditions Genes on X chromosome, so
    more common in men.
  • Protanopia, missing red photopigment
  • Deuteranopia, missing green photopigment
  • Non-sex-linked condition
  • Tritanopia, missing blue photopigment o
  • monochromats people who are totally colorblind,
    more severe

91
Color Vision Systems
Tritanopia deuteranopia protanopia
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IV Dark Adaptation and Light Adaptation
94
Range of luminance to which the human eye respond
Millilambert,???
95
Dark Adaptation
  • The decline in visual threshold in a dimly
    lighted environment
  • First phase
  • Neural adaptation
  • Second phase
  • chemical adaptation
  • depleted of rhodopsin in bright light
  • replenish their rhodopsin in dim light

96
Light Adaptation When one passes suddenly from a
dim to a brightly lighted environment, the light
seems intensely and even uncomfortably bright
until the eyes adapt to the increased
illumination and the visual threshold rises.
Mechanism?
97
Section IV The Auditory System
98
Part I Structure of the Ear
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  • 1. Outer Ear
  • Pinna (auricle) directs sound waves into the
    auditory canal
  • Auditory Canal conducts sound to the eardrum
  • Tympanic membrane (Eardrum) thin membrane that
    vibrates in response to sound, transfers sound
    energy to bones of the middle ear

101
  • 2. Middle Ear three tiny bones amplify sound
    and transfer sound energy to the inner ear
  • A Malleus
  • B Incus
  • C Stapes
  • Ossicles are smallest bones in the body
  • Act as a lever system
  • Footplate of stapes enters oval window of the
    cochlea

102
  • 3. InnerWhere Sound Energy is Transduced
  • Cochlea snail shaped fluid-filled structure
  • Oval window thin membrane, transfers vibrations
    from stapes to fluid of cochlea

103
  • Basilar membrane runs the length of the cochlea
  • Organ of Corti rests on basilar membrane,
    contains receptor cells
  • Round window absorbs energy and equalizes
    pressure in the cochlea

104
4. Pathway Transmitting Sound Wave from External
Environment to Inner Ear
Air Conduction
Sound wave
Sound wave
Auditory Canal
Auditory Canal
Air in tympanic cavity
Tympanic membrane
Bone Conduction
Ossicular chain
Round window
Sound wave
Oval window
Inner ear
Vibration of skull
105
Part 2. Properties of Sound
  • Sound travels in waves as does light
  • 1. Pitch determined by frequency, the number
    of cycles per second of a sound wave, measured in
    hertz (Hz)
  • 2. Loudness determined by amplitude (height)
    of the sound wave, measured in decibels (dB)
  • 3. Timbre determined by complexity and shape
    of the sound wave, gives each sound its unique
    quality

106
Loudness of Sound
  • 0 dB hearing threshold
  • 50 dB normal conversation
  • 90 dB danger zone
  • 120 dB Rock concert
  • 130 dB Pain threshold

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109
Part 3 Role of Middle Ear in Sound Transmission
110
Mechanisms Involved in Transformer Process
  • Size difference between Tympanic Membrane and
    Stapes Footplate
  • Lever action

111
First Component of Middle Ear Transformer Action
  • Size Difference
  • Tympanic membrane
  • .59 cm2
  • Stapes footplate
  • .032 cm2
  • Pressure formula
  • Pressure force/area
  • Impact on sound transmission

Pressure gain 0.59/0.032 18.4 (times)
112
Transformer Action of Middle EarLever Action
  • Fulcrum Effect pressure gain 1.3
    times

113
TRANSFORMER ACTION AMOUNT OF AMPLIFICATION
Pressure Gain Contribution from 18.4 TM
(Tympanic Membrane) to stapes footplate
1.3 Lever action 23.9 Total pressure
gain (18.6 x 1.3)
114
Part 4 Function of Organ of Corti
  • a structure rests atop the basilar membrane along
    its length
  • contains approx. 16,000 cochlear hair cells

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116
1. How to discriminate the frequency of the
sound? --- Traveling Wave Theory
117
Vibration of Basilar Membrane and the Traveling
Wave Theory
  • Sound wave entering at the oval window cause the
    basilar membrane to vibrate
  • different frequencies cause vibrations at
    different locations (places) along basilar
    membrane
  • higher frequencies at base, lower frequencies at
    top

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120
2. Electrical Potentials
  • DC vs. AC
  • Direct Current (DC) stimulus doesnt change
    with time, constant i.e. battery
  • Alternating Current (AC) always changing over
    time, looks like a sine wave

121
Cochlea
  • Perilymph-
  • similar in composition to extracellular fluid.
  • High in Na and low in K.
  • Endolymph-
  • found in the scala media.
  • Similar to intracellular fluid. High in K and
    low in Na

122
Two DC Potentials (EP)
  • Endocochlear Potential (EP)
  • 80 mV potential with respect to a neutral point
    on the body
  • due to the Stria Vascularis (????????)

123
80 mV
Reticular Lamina
-80 mV
Two DC Potentials (IP)
  • Intracellular Potential (IP) or organ of corti
    potential (resting potential)
  • Recorded -80 mV inside cells of organ of corti

124
Hair Cell in the Organ of Corti
When the basilar membrane moves, a shearing
action between the tectorial membrane and the
organ of Corti causes hair cells to bend
125
There are mechanical gates on each hair cell that
open when they are bent.
K comes into the hair cell and depolarizes the
hair cell.
126
Two AC Potentials
  • Cochlear Microphonic Potential
  • Reproduces frequency and waveform of a sinusoid
    perfectly
  • Generated from hair cell
  • Action Potential (AP)
  • Electrical activity from the VIII Nerve
  • Can be measured from anywhere in the cochlea or
    in the auditory nerve

127
Part 5 Deafness
  • Conduction deafness -
  • possible causes include perforated eardrum,
    inflammation, otosclerosis
  • Sensineural deafness - nerve damage
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