PSYC 367: Quiz 2

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what is somatosenstion?

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1

what is somatosenstion?

the process of neural substrates being activated by physical stimuli resulting in perception of

  • touch

  • Kinesthesis

  • temperature

  • pain

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what is touch?

sensations caused by mechanical displacements of the skin

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what is kinesthesis?

perception of position and movement of limbs in space

  • Part of proprioception (also includes internal sensation)

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what are somatosensory receptors?

neurons with peripheral and central axons - some touch receptors have specialized endings in the skin

<p>neurons with peripheral and central axons - some touch receptors have specialized endings in the skin</p>
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what is glabrous skin?

skin with no hair follicles - palms, soles, lips

<p>skin with no hair follicles - palms, soles, lips</p>
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what is a mechanoreceptor?

sensory neuron that responds to mechanical stimulation

  • 4 types in glabrous skin

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what are receptive fields in the skin?

body areas that elicit responses from sensory neurons

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mechanoreceptor type SA 1 (Merkel)

  • size of receptive field = small

  • adaptation rate to new stimulus = slow

  • max feature sensitivity = small slow sustained pressure, very low frequency (< ~5 Hz)

  • primary perceptual functions = coarse texture and pattern

<ul><li><p>size of receptive field = small</p></li><li><p>adaptation rate to new stimulus = slow</p></li><li><p>max feature sensitivity = small slow sustained pressure, very low frequency (&lt; ~5 Hz)</p></li><li><p>primary perceptual functions = coarse texture and pattern</p></li></ul><p></p>
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mechanoreceptor type FA I (Meissner)

  • size of receptive field = small

  • adaptation rate to new stimulus = fast

  • max feature sensitivity = small fast temporal changes in skin deformation (~5 to 50 Hz) - skin slip

  • primary perceptual functions = low-frequency vibration; grasp stability (fingers, lips - light touch)

<ul><li><p>size of receptive field = small</p></li><li><p>adaptation rate to new stimulus = fast</p></li><li><p>max feature sensitivity = small fast temporal changes in skin deformation (~5 to 50 Hz) - skin slip</p></li><li><p>primary perceptual functions = low-frequency vibration; grasp stability (fingers, lips - light touch)</p></li></ul><p></p>
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mechanoreceptor SA II (Ruffini)

  • receptive field = large

  • adaptation rate to new stimulus = slow

  • max feature sensitivity = large slow sustained downward pressure; lateral skin stretch (~5-50 Hz)

  • primary perceptual functions = finger position

<ul><li><p>receptive field = large</p></li><li><p>adaptation rate to new stimulus = slow</p></li><li><p>max feature sensitivity = large slow sustained downward pressure; lateral skin stretch (~5-50 Hz)</p></li><li><p>primary perceptual functions = finger position</p></li></ul><p></p>
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mechanoreceptor FA II (Pacinian)

  • size of receptive field = large

  • adaptation rate to new stimulus = fast

  • max feature sensitivity = large fast temporal changes in skin deformation (50-700 Hz)

  • primary functions = high-frequency vibration; fine texture

<ul><li><p>size of receptive field = large</p></li><li><p>adaptation rate to new stimulus = fast</p></li><li><p>max feature sensitivity = large fast temporal changes in skin deformation (50-700 Hz)</p></li><li><p>primary functions = high-frequency vibration; fine texture</p></li></ul><p></p>
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hair follicle receptor

5th type of fast-adapting tactile mechanoreceptor in hairy skin

<p>5th type of fast-adapting tactile mechanoreceptor in hairy skin</p>
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what are kinesthetic mechanoreceptors?

information in skeleton, muscles, tendons of human body (force, torque, position, velocity)

  • muscle spindle

  • golgi tendon organ

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what are muscle spindles?

mechanoreceptors that signal length and changes in length of muscles (stretched and shortened)

<p>mechanoreceptors that signal length and changes in length of muscles (stretched and shortened)</p>
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what are golgi tendon organs?

mechanoreceptors that respond to changes in muscle tension and joint position (rather than muscle stretch)

<p>mechanoreceptors that respond to changes in muscle tension and joint position (rather than muscle stretch)</p>
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what are nociceptors?

free nerve endings that initiate pain feelings

<p>free nerve endings that initiate pain feelings</p>
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what are thermoreceptors?

free nerve endings that stimulate feelings of temperature (closer to the skin)

<p>free nerve endings that stimulate feelings of temperature (closer to the skin)</p>
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what is our physiological zero?

normal skin temperature (30-36 degrees)

  • feel no sensations of warmth or cold

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what do different thermoreceptor firing rates look like?

  • warmth fibres: increase firing rate with increases in skin temperature above 36 degrees

  • cold fibres: increase firing rate with decreases in skin temperature below 30 degrees

<ul><li><p>warmth fibres: increase firing rate with increases in skin temperature above 36 degrees</p></li><li><p>cold fibres: increase firing rate with decreases in skin temperature below 30 degrees</p></li></ul><p></p>
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what stimulates nociceptors?

  • extreme temperature (thermal type)

  • severe pressure or excessive stretching (mechano type)

  • intense heat, chemicals released by injured tissues, and/or spicy food (polymodal type)

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how does the transduction of somatosensory signals work?

not fully known - occurs in peripheral axon, channels are sensitive to mechanical force/temperature/chemicals released by injured tissue open and Na+/Ca+ enter

  • neuron depolarizes (receptor potential) - action potential travels full length of axon to spinal cord if threshold is reached

<p>not fully known - occurs in peripheral axon, channels are sensitive to mechanical force/temperature/chemicals released by injured tissue open and Na+/Ca+ enter</p><ul><li><p>neuron depolarizes (receptor potential) - action potential travels full length of axon to spinal cord if threshold is reached</p></li></ul><p></p>
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what transports somatosensory info to spinal cord?

4 different-sized nerve fibres

  • proprioceptor

  • mechanoreceptor

  • pain and temperature

  • pain, temperature, itch

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proprioceptor

  • A-alpha fibre - thick myelin and axon

  • diameter = 13-20 micrometer

  • conduction speed = 80-120 m/s

<ul><li><p>A-alpha fibre - thick myelin and axon</p></li><li><p>diameter = 13-20 micrometer</p></li><li><p>conduction speed = 80-120 m/s</p></li></ul><p></p>
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mechanoreceptor

  • A-beta fiber - mildly thick myelin and axon

  • diameter = 6-12 micrometers

  • conduction speed = 35-75 m/s

  • 3 types: fast-adapting, slowly adapting II (only glabrous skin), slowly adapting I

<ul><li><p>A-beta fiber - mildly thick myelin and axon</p></li><li><p>diameter = 6-12 micrometers</p></li><li><p>conduction speed = 35-75 m/s</p></li><li><p>3 types: fast-adapting, slowly adapting II (only glabrous skin), slowly adapting I</p></li></ul><p></p>
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pain and temperature receptor

  • A-delta - thin myelin and smaller axon

  • diameter = 1-5 micrometers

  • conduction speed = 5-30 m/s

  • One type: A-delta (only in hairy skin - hair receptor)

<ul><li><p>A-delta - thin myelin and smaller axon</p></li><li><p>diameter = 1-5 micrometers</p></li><li><p>conduction speed = 5-30 m/s</p></li><li><p>One type: A-delta (only in hairy skin - hair receptor)</p></li></ul><p></p>
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pain, temperature, itch fiber

  • C - no myelin and smallest axon

  • diameter = 0.2-1.5 micrometers

  • conduction speed (m/s) = 0.5-2

  • two types: C-nociceptor, C-tactile (only hairy skin)

<ul><li><p>C - no myelin and smallest axon</p></li><li><p>diameter = 0.2-1.5 micrometers</p></li><li><p>conduction speed (m/s) = 0.5-2</p></li><li><p>two types: C-nociceptor, C-tactile (only hairy skin)</p></li></ul><p></p>
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what is double pain?

initial sharp pain followed by slower, throbbing pain

  • A-delta fibre = first sharp pain

  • C fibre = throbbing pain

<p>initial sharp pain followed by slower, throbbing pain</p><ul><li><p>A-delta fibre = first sharp pain</p></li><li><p>C fibre = throbbing pain</p></li></ul><p></p>
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what types of fibres are A-delta fibres?

  • cold fibres

  • thermal nociceptors (TRPM8 channels, extreme cold)

  • mechano nociceptors (severe pressure)

<ul><li><p>cold fibres</p></li><li><p>thermal nociceptors (TRPM8 channels, extreme cold)</p></li><li><p>mechano nociceptors (severe pressure)</p></li></ul><p></p>
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what types of fibres are C fibres?

  • warmth fibres

  • polymodal nociceptors: inflammatory cells release prostaglandin, bradykinin or portions which activate their respective channels

  • intense heat, protons and capsaicin (in hot peppers) = capsaicin receptors (TRPV1)

<ul><li><p>warmth fibres</p></li><li><p>polymodal nociceptors: inflammatory cells release prostaglandin, bradykinin or portions which activate their respective channels</p></li><li><p>intense heat, protons and capsaicin (in hot peppers) = capsaicin receptors (TRPV1)</p></li></ul><p></p>
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what are the types of chemical membrane receptors on C fibres (polymodal nociceptor)?

  • capsaicin receptor and ASIC: reduce pain accompanying inflammation

  • TTX-resistant sodium channels: silence signalling by nociceptors

  • bradykinin receptor: ease pain related to inflammation

  • prostaglandin producing enzymes: aspirin, ibuprofen, COX-2 inhibitors reduce prostaglandin production

<ul><li><p>capsaicin receptor and ASIC: reduce pain accompanying inflammation</p></li><li><p>TTX-resistant sodium channels: silence signalling by nociceptors</p></li><li><p>bradykinin receptor: ease pain related to inflammation</p></li><li><p>prostaglandin producing enzymes: aspirin, ibuprofen, COX-2 inhibitors reduce prostaglandin production</p></li></ul><p></p>
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significance of the dorsal root ganglion of spinal cord to pain perception?

cell bodies of A-beta, C, A-delta fibres are located there

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significance of dorsal horn of spinal cord to pain perception?

many central axons combine into a single nerve trunk and synapse there - different types of somatosensory nerve fibres project to different layers of it

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what are the somatosensory layers of the dorsal horn?

I = A-delta nociceptors

I-II = C/A delta fibres

II = C fibres (substantia gelatinosa)

II-III = A-delta hair follicle afferents

II-V = A-beta hair follicle and tactile afferents

<p>I = A-delta nociceptors</p><p>I-II = C/A delta fibres</p><p>II = C fibres (substantia gelatinosa)</p><p>II-III = A-delta hair follicle afferents</p><p>II-V = A-beta hair follicle and tactile afferents</p>
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what is the process of our reflex loop?

  1. noxious stimulus

  2. info travels in to dorsal horn of spinal cord

  3. interneuron connects sensory and motor neurons

  4. motor neuron controls movement (ex. withdraw finger)

  • spinothalamic and dorsal column-medial lemniscal pathways contain neurons that participate

<ol><li><p>noxious stimulus</p></li><li><p>info travels in to dorsal horn of spinal cord</p></li><li><p>interneuron connects sensory and motor neurons</p></li><li><p>motor neuron controls movement (ex. withdraw finger)</p></li></ol><ul><li><p>spinothalamic and dorsal column-medial lemniscal pathways contain neurons that participate</p></li></ul><p></p>
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what is the somatosensory pathway for touch?

  1. spinal cord (1st synapse for some neurons)

  2. medulla (1st synapse for most neurons)

  3. thalamus (synapse)

  4. parietal cortex (synapse)

<ol><li><p>spinal cord (1st synapse for some neurons)</p></li><li><p>medulla (1st synapse for most neurons)</p></li><li><p>thalamus (synapse)</p></li><li><p>parietal cortex (synapse)</p></li></ol><p></p>
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what is the head only somatosensory pathway for touch?

  1. pons (1st synapse): principal sensory nucleus of trigeminal nerve

  2. thalamus (2nd synapse): ventral posteromedial nucleus (VPM)

  3. parietal cortex (3rd synapse)

<ol><li><p>pons (1st synapse): principal sensory nucleus of trigeminal nerve</p></li><li><p>thalamus (2nd synapse): ventral posteromedial nucleus (VPM)</p></li><li><p>parietal cortex (3rd synapse)</p></li></ol><p></p>
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what is the somatosensory pathway for temperature and pain?

spinothalamic pathway

  1. peripheral skin/tissue experiencing painful stimuli

  2. nociceptors travel from injury sight to dorsal root ganglion

  3. substantia gelatinosa (layer II) in dorsal horn (1st synapse)

  4. thalamus (2nd synapse)

  5. parietal cortex (3rd synapse)

<p>spinothalamic pathway</p><ol><li><p>peripheral skin/tissue experiencing painful stimuli</p></li><li><p>nociceptors travel from injury sight to dorsal root ganglion</p></li><li><p>substantia gelatinosa (layer II) in dorsal horn (1st synapse)</p></li><li><p>thalamus (2nd synapse)</p></li><li><p>parietal cortex (3rd synapse)</p></li></ol><p></p>
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what is the head only somatosensory pathway for temperature and pain?

  1. medulla (1st synapse)

  2. thalamus (2nd synapse)

  3. parietal cortex (3rd synapse)

<ol><li><p>medulla (1st synapse)</p></li><li><p>thalamus (2nd synapse)</p></li><li><p>parietal cortex (3rd synapse)</p></li></ol><p></p>
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what is the S1 region in the brain?

“light blue” portion of the somatosensory cortex

  • Includes Brodmann areas 3a, 3b, 1 and 2 (a way of mapping the cortex/functions - numbering is not in directional order)

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Brodmann area 3

where neurons from thalamus synapse - layer 4 of area 3a (proprioception) or 3b (touch)

  • each type of mechanocreceptor connects to different column in 3b (in pic)

  • projects to area 1 and 2

<p>where neurons from thalamus synapse - layer 4 of area 3a (proprioception) or 3b (touch)</p><ul><li><p>each type of mechanocreceptor connects to different column in 3b (in pic)</p></li><li><p>projects to area 1 and 2</p></li></ul><p></p>
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What is the S2 region of the brain?

“dark blue” portion of the somatosensory cortex

<p>“dark blue” portion of the somatosensory cortex</p>
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what is the somatotopic map/sensory homunculus

map of each point on skin represented by a corresponding area in contralateral cortex (map is distorted)

<p>map of each point on skin represented by a corresponding area in contralateral cortex (map is distorted)</p>
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what is cortical magnification?

enlarged representation in cortical somatotopic map/sensory homunculus relative to skin area

  • multiple maps in S1 and S2

  • S1, area 1 = middle

  • S1, area 2 = right

  • S1, area 3 = left

<p>enlarged representation in cortical somatotopic map/sensory homunculus relative to skin area</p><ul><li><p>multiple maps in S1 and S2</p></li><li><p>S1, area 1 = middle</p></li><li><p>S1, area 2 = right</p></li><li><p>S1, area 3 = left</p></li></ul><p></p>
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what is tactile sensitivity?

touch detection ability (inverse of absolute threshold - high sensitivity = low threshold, low sensitivity = high threshold)

  • highest on face

  • lowest on foot

<p>touch detection ability (inverse of absolute threshold - high sensitivity = low threshold, low sensitivity = high threshold)</p><ul><li><p>highest on face</p></li><li><p>lowest on foot</p></li></ul><p></p>
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What entails touch discrimination?

JND increases with magnitude of standard stimulus (Weber) - smaller (better discrimination) for areas of skin with higher sensitivity (lower absolute threshold)

  • Weber fraction for touch: JND/standard

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what is touch acuity?

minimum distance at which two stimuli are just perceptible as separate - 2-point threshold

  • better in skin regions with larger cortical representation in homunculus

  • can be low when detection threshold is high

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how are somatosensory neurons represented in receptive fields?

each one in S1 responds to stimulation in only a specific small area of body

  • A region (image) = excitatory centre (middle of stimulation spot)

  • B region = inhibitory surround (around stimulation spot)

<p>each one in S1 responds to stimulation in only a specific small area of body</p><ul><li><p>A region (image) = excitatory centre (middle of stimulation spot)</p></li><li><p>B region = inhibitory surround (around stimulation spot)</p></li></ul><p></p>
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2-point threshold on body parts with small receptive fields?

2 points stimulate separate receptive fields, 2 points perceived (thumb)

<p>2 points stimulate separate receptive fields, 2 points perceived (thumb)</p>
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2-point threshold on body parts with larger receptive fields

2 points stimulate same receptive field, 1 point perceived

<p>2 points stimulate same receptive field, 1 point perceived</p>
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what is Aristotle’s Illusion?

2 receptive fields far apart on cortex are stimulated, but this normally only happens when 2 objects touch you

failure of illusion: receptive fields close on cortex may be stimulated, but this normally only happens when 2 objects touch you

<p>2 receptive fields far apart on cortex are stimulated, but this normally only happens when 2 objects touch you</p><p>failure of illusion: receptive fields close on cortex may be stimulated, but this normally only happens when 2 objects touch you</p>
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what is nociceptive pain?

results from stimulation of free nerve endings in skin, muscles, and joints - aids survival by avoiding potentially harmful stimuli, immobilize to promote healing

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what are the neuro components of pain?

  1. limbic system (anterior cingulate, insula, amygdala): processing of emotion

  2. prefrontal cortex: modulating pain perception, chronic pain emotional response

  • based on more than just sensory factors

<ol><li><p>limbic system (anterior cingulate, insula, amygdala): processing of emotion</p></li><li><p>prefrontal cortex: modulating pain perception, chronic pain emotional response</p></li></ol><ul><li><p>based on more than just sensory factors</p></li></ul><p></p>
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what modulates pain sensitivity?

enkephalins and endorphins (endogenous opiates) - released by descending inputs from brain (ex. periaqueductal gray in midbrain)

  • block release of substance P

<p>enkephalins and endorphins (endogenous opiates) - released by descending inputs from brain (ex. periaqueductal gray in midbrain)</p><ul><li><p>block release of substance P</p></li></ul><p></p>
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where do pain neurons transmit signals?

synapse in substantia gelatinosa

  • neuron from brain + C fibre from skin + spinal cord neuron to thalamus

  • C fibre transmits signals to brain dendrites an releases nt substance P

  • substance P membrane receptors are on spinal cord neuron (why athlete’s don’t notice minor injuries for hours)

<p>synapse in substantia gelatinosa</p><ul><li><p>neuron from brain + C fibre from skin + spinal cord neuron to thalamus</p></li><li><p>C fibre transmits signals to brain dendrites an releases nt substance P</p></li><li><p>substance P membrane receptors are on spinal cord neuron (why athlete’s don’t notice minor injuries for hours)</p></li></ul><p></p>
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what is gate control theory?

based on interactions between fast A-beta touch fibres and slow C/A-delta pain fibres - substantia gelatinosa in dorsal horn gates flow of pain to brain, descending inputs from brain can’t close pain gate

  • transmission cells carry pain signal to brain when gate is open

  • fast mechanoreceptors = close gate

  • slow nociceptors = open gate

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how can you treat nociceptive pain?

  • transcutaneous electrical nerve stimulation (TENS)

  • anesthetics

  • analgesics

  • acupuncture

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transcutaneous electrical nerve stimulation (TENS)

based on gate control theory - electric current passed through skin near pain site → activates A-beta fibres to close pain gate → stimulates release of endogenous opiates

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anesthetics

produce total loss of sensation by interrupting signals travelling to brain

  • local: act at site of injection - block Na channels

  • general: act on full brain (unconsciousness)

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analgesics

produces loss of pain sensations

  • non-opiate: mild/moderate pain - aspirin/ibuprofen (anti-inflammatory) and acetaminophen/COX-2 inhibitors (Tylenol, Celebrex)

  • opiate: potent pain killers - morphine, codeine, heroin (block nociceptor nt release and inhibit spin neurons)

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acupuncture

insertion of long needles into specific places - not understood but may release endogenous opiates

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what is inflammatory pain?

when nociceptors become increasingly sensitized due to damage/inflammation of tissues or by tumour cells

  • Hyperalgesia and allodynia

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hyperalgesia

Painful stimuli become more painful due to nociceptors becoming sensitized and overly reactive to noxious stimuli

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allodynia

gentle touch stimuli become painful - lower thresholds for pain

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what is neuropathic pain?

more serious than inflammatory, chronic - not related to stimulation of nociceptors

  • burning, shooting pain, numbness, itchiness

  • Damage/dysfunction to CNS or PNS

  • characterized by peripheral or central sensitization

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peripheral sensitization

change in nociceptors coming into spinal cord

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central sensitization

increase of number of pain receptors, rewiring of connections or loss of inhibitory cells in spinal cord

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What are treatments for persistent pain?

  • anticonvulsants

  • Capsaicin

  • Marijuana

  • NMDA-receptor blockers

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Anticonvulsants

inhibit specific calcium channel to prevent release of nociceptors neurotransmitters

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capsaicin

stimulates nociceptors, but may kill them/use up supply of neurotransmitters causing pain initially but then relieves pain

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marijuana

cannabinoids block nt release from nociceptors and reduce inflammation

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NMDA-receptor blockers

prevent glutamate from binding with NMDA receptors on spinal cord neurons (involved in central sensitization)

  • cocaine and heroin - activate nociceptor receptors to block glutamate release

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what is phantom limb syndrome?

when sensations are perceived to come from an amputated limb, neuropathic pain

  • central sensitization rewiring occurs during surgery

  • local anesthetic should reduce central sensitization, but it still occurs

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how does phantom limb syndrome work? (ex. hand amputation)

the hand is normally flanked below by face representation and above by upper arm representation in the cortical homunculus - following amputation face and arm regions take over hand region of cortex → touching of face and upper arm = pain in missing hand

<p>the hand is normally flanked below by face representation and above by upper arm representation in the cortical homunculus - following amputation face and arm regions take over hand region of cortex → touching of face and upper arm = pain in missing hand</p>
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how to treat phantom limb pain?

  • mirror box - move uninjured limb in front of mirror to act like the missing limb

  • electrical stimulation in spinal dorsal column to close pain gate in spine

<ul><li><p>mirror box - move uninjured limb in front of mirror to act like the missing limb</p></li><li><p>electrical stimulation in spinal dorsal column to close pain gate in spine</p></li></ul><p></p>
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what is light?

a wave/stream of photons/tiny particles (when wave gets absorbed by retina) that each consist of one quantum energy

  • what we can see = electromagnetic spectrum

<p>a wave/stream of photons/tiny particles (when wave gets absorbed by retina) that each consist of one quantum energy</p><ul><li><p>what we can see = electromagnetic spectrum</p></li></ul><p></p>
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what wavelengths are visible to the human eye?

between 400-700nm (nanometer [nm] = 10^-9m)

  • wavelength determines colour perceived (ROYGBIV)

<p>between 400-700nm (nanometer [nm] = 10^-9m)</p><ul><li><p>wavelength determines colour perceived (ROYGBIV)</p></li></ul><p></p>
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what is vision intensity?

depends on wave property (height of energy wave peaks - amplitude) and particle property (number of quanta emitted by a light source)

  • independent, but correlated

  • perceived brightness

<p>depends on wave property (height of energy wave peaks - amplitude) and particle property (number of quanta emitted by a light source)</p><ul><li><p>independent, but correlated</p></li><li><p>perceived brightness</p></li></ul><p></p>
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what is the emission spectra of light sources?

  • sunlight = short wavelengths (blue) (florescent lightbulbs more similar to)

  • light bulbs = long wavelengths (yellow)

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what happens to light once it is emitted?

  1. absorbed: not transmitted at all

  2. diffracted: scattered by dust/water particles in air

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what happens once light encounters a surface?

  1. transmitted: conveyed from one place to another, usually with refraction (colour of translucent

  2. absorbed: medium heats up

  3. reflected: redirected back to origin (colour of solid objects depends on wavelengths reflected off object to eye)

<ol><li><p>transmitted: conveyed from one place to another, usually with refraction (colour of translucent </p></li><li><p>absorbed: medium heats up</p></li><li><p>reflected: redirected back to origin (colour of solid objects depends on wavelengths reflected off object to eye)</p></li></ol><p></p>
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what is refraction?

change in direction (bending) of light ray passing from one transmitting medium to another - also depends on wavelength of the source

  • violet refracts the most

  • red refracts the least

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pupil

eye opening, light energy passes through

<p>eye opening, light energy passes through</p>
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sclera

protective white outer surface of eye

<p>protective white outer surface of eye</p>
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iris

outer pigmented layer, inner layer of blood vessels

<p>outer pigmented layer, inner layer of blood vessels</p>
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cornea

covers iris and pupil, very sensitive to touch

<p>covers iris and pupil, very sensitive to touch</p>
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ciliary muscle

controls shape of lens

<p>controls shape of lens</p>
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aqueous humour

fluid in anterior chamber, continually replenished

<p>fluid in anterior chamber, continually replenished</p>
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virtuous humour

fluid in posterior chamber, not replenished, floaters form

<p>fluid in posterior chamber, not replenished, floaters form</p>
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choroid

blood vessels in eye, nourishes retina

<p>blood vessels in eye, nourishes retina</p>
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retina

detects light and initiates neural messages

<p>detects light and initiates neural messages</p>
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macula

process what is in front of us, yellow pigmented spot

<p>process what is in front of us, yellow pigmented spot</p>
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fovea

depression in retina where visual acuity is highest

  • light passes through shallowest layer

  • centre = only cones, densely packed

  • away = more rods and fewer cones, less dense

<p>depression in retina where visual acuity is highest</p><ul><li><p>light passes through shallowest layer</p></li><li><p>centre = only cones, densely packed</p></li><li><p>away = more rods and fewer cones, less dense</p></li></ul><p></p>
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optic disc

point of exit for axons leaving eye

<p>point of exit for axons leaving eye</p>
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optic nerve (III)

send visual messages to brain to help you see

<p>send visual messages to brain to help you see</p>
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95

what parts of the eye are for seeing?

  • optical apparatus: cornea, aqueous humour, lens, vitreous humour, iris

  • neural apparatus: retina - macula, fovea, optic disc, blood vessels

<ul><li><p>optical apparatus: cornea, aqueous humour, lens, vitreous humour, iris</p></li><li><p>neural apparatus: retina - macula, fovea, optic disc, blood vessels</p></li></ul><p></p>
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96

what does the optical apparatus do?

light emitted is transmitted or reflected to eye and is then transmitted through cornea, aqueous humour, lens, and vitreous humour → image is focused on the retina (photoreceptors absorb light)

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97

what does sharpness of an image depend o?

2/3 ability of cornea, 1/3 ability of lens, aqueous, and vitreous humours to refract light

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98

what does the eye look like in a relaxed state?

farther away is in focus, nearer is blurred

<p>farther away is in focus, nearer is blurred</p>
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99

accommodation

process by which eye changes its focus by changing shape of the lens

  • fatter lens = increase of optical power of eye to bring images of near objects into focus (like a camera lens)

<p>process by which eye changes its focus by changing shape of the lens</p><ul><li><p>fatter lens = increase of optical power of eye to bring images of near objects into focus (like a camera lens)</p></li></ul><p></p>
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100

cataract

opacity of crystalline lens of eye can be congenital or develop in later adulthood - interferes with retinal image quality

  • treated by surgical removal and replacement of lens

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