Title: Sensory%20Function%20of%20the%20Nervous%20System
1Chapter 31
- Sensory Function of the Nervous System
2Contents
- Sensory receptors and sensory organs
- Pain
- The visual system
- The Auditory Systems
3Section 1Sensory Receptor and Sensory Organ
4Part 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
5Spectrum of the Electromagnetic Wave
6Somatic Sensory Nerve Endings
7Free Nerve Endings
- dendrites interspersed among other cells/tissues
- pain, temperature, touch
8Encapsulated Nerve Endings
- dendrites with special supporting structures
- mechanoreceptors and proprioceptors
9Classification 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.
10Classification 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
11Classification 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
12Which receptor?
13Sequence of Events in a Receptor
Basic Function
Stimulus
Amplification
14Part 2 Properties of the Receptors
- Adequate Stimulus
- Transduction
- Adaptation
- Encoding
151. 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
162. 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
17Receptor Potential and Generator Potential
183. 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
19Phasic 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.
204. Encoding
- The quality of the stimulus is encoded in the
frequency of the action potentials.
21Stretch 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
22Summary
- 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.
23Section 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
25Why 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
261. Nociceptors
- special receptors that respond only to noxious
stimuli and generate nerve impulses which the
brain interprets as "pain".
27Nociopectors
- 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
292. 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
303. 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)
344. 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
35Afferent 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
36Referred pain
- Pain originating from organs perceived as coming
from skin - Site of pain may be distant from organ
37Convergence 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.
385. 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(No Transcript)
40How 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
41Applications 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
426. 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.
43Section 3
44Part 1. Structure of the Eyeball
45Part2 Focusing on the Retina
- The images of objects in the environment are
focused on the retina.
461. 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.
47Light 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.
482. 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
493. 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)
51Focusing
Muscles relaxed Lens less spherical Focus far
Muscles working Lens more spherical Focus near
52(No Transcript)
53(No Transcript)
54(No Transcript)
55Near 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
56Diopter???
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
594. Error of Refraction
- Caused by
- shape of eye
- power of lens
60Farsightedness
- less common
- eye too short and/or lens too weak
- light focuses behind retinal
- correct with convex lens to add power
61FARSIGHTEDNESS (HYPEROPIA)
UNCORRECTED
CORRECTED
62Nearsightedness
- 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
63NEARSIGHTEDNESS (MYOPIA)
UNCORRECTED
CORRECTED
64- Astigmatism
- abnormal curvature of the cornea
- Light from vertical and horizontal direction do
not focuses in the same point
65Oldsightedness (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.
66The loss in power of accommodation is most
significant and dramatic between the ages of 40
and 50
67Part 3 Function of the Retina
68I. 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.
69Distribution of the cones and rods on the retina.
70Rods
- 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
71Cones
- 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
72Cones see detail but require bright light Rods
see in low light but lack detail
73Evidence 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
74II Transduction of Light Energy by Rod Cell
75(No Transcript)
761. 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
77Retinal Light Sensitive Pigment11-cis-Retinal
- All-trans-Retinal
Light
Dark
all-trans retinal (straight chain form)
11-cis retinal (bent shape form)
78(No Transcript)
79Converting 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
8011-cis retinal opsin
all-trans retinal opsin
rhodopsin
isomerase
All-trans retinal
11-cis retinal
opsin
opsin
81Vitamin 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.
822. Receptor Potential of Rods Hyperpolarization
83(No Transcript)
84 III Color Vision
85Photochemistry of Color Vision by Cones
- Three kinds of proteins on the photopigments
- Sensitive to three kinds of light
- Trichromatic Theory
86Visible spectrum 380-760 nm (nm is a billionth
of a meter)
87Trichromatic 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
88Color Sensitivity of Different Cones
89Primary Colors
- Red, Green and Blue
- can be mixed to produce any other color
90Color 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
91Color Vision Systems
Tritanopia deuteranopia protanopia
92(No Transcript)
93IV Dark Adaptation and Light Adaptation
94Range of luminance to which the human eye respond
Millilambert,???
95Dark 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
96Light 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?
97Section IV The Auditory System
98Part I Structure of the Ear
99(No Transcript)
100- 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
1044. 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
105Part 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
106Loudness of Sound
- 0 dB hearing threshold
- 50 dB normal conversation
- 90 dB danger zone
- 120 dB Rock concert
- 130 dB Pain threshold
107(No Transcript)
108(No Transcript)
109Part 3 Role of Middle Ear in Sound Transmission
110Mechanisms Involved in Transformer Process
- Size difference between Tympanic Membrane and
Stapes Footplate - Lever action
111First 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)
112Transformer Action of Middle EarLever Action
- Fulcrum Effect pressure gain 1.3
times
113TRANSFORMER 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)
114Part 4 Function of Organ of Corti
- a structure rests atop the basilar membrane along
its length - contains approx. 16,000 cochlear hair cells
115(No Transcript)
1161. How to discriminate the frequency of the
sound? --- Traveling Wave Theory
117Vibration 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
118(No Transcript)
119(No Transcript)
1202. 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
121Cochlea
- 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
122Two DC Potentials (EP)
- Endocochlear Potential (EP)
- 80 mV potential with respect to a neutral point
on the body - due to the Stria Vascularis (????????)
12380 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
124Hair 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
125There are mechanical gates on each hair cell that
open when they are bent.
K comes into the hair cell and depolarizes the
hair cell.
126Two 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
127Part 5 Deafness
- Conduction deafness -
- possible causes include perforated eardrum,
inflammation, otosclerosis - Sensineural deafness - nerve damage