week 3 (touch + pain) Flashcards

(27 cards)

1
Q

define: primary somatosensory cortex (where, what)

A
  • receives input from thalamus via internal capsule
  • postcentral gyrus
  • parietal lobe
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2
Q

define: secondary somatosensory cortex (where, what)

A
  • receives info from S1 (primaary somatosensory cortex)
  • bottom part near S1
    ⤷ more towards middle of brain but still parietal lobe
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3
Q

question: where are the motor areas of the cortex?

A
  • ## precentral gyrus
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4
Q

name + explain: types of body representation in S1 (2)

A

1. somatotopic organization
- orderly representation of body
- adjacent areas on skin connect to adjacent areas in brain
- contralateral

nonlinear representation
- sensory homunculus
- RF size dep. on location in somatotopic map
- smaller RF have larger areas in S1

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5
Q

explain: columnar organization of cerebral cortex
question: what layer does somatosensory input arrive at?

A
  • 6 layers
  • (info from thalamus) somatosensory arrives at layer 4

**1, 2, 3a, 3b are areas of the S1, not layers (they span all 6 layers of cortex)

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6
Q

define: neural plasticity

A
  • changes in cortical map can occur in resp. to physiological changes in sensory and motor function
  • ex. remapping after practicing, exp., injury
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7
Q

define: cross-modal plasticity

A
  • 1 sensory system taken over by another
  • if the sys. is inhibited/unable to work
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8
Q

explain: phantom limbs

A
  • illusion that missing limb is still present
  • functional remapping changes somatotopic map
    ⤷ S1neurons that lose input get innervated by receptors for a diff. area
  • ex. amputate arm -> S1 neurons that lost input are innervated by face receptors
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9
Q

question: does a higher threshold mean that part of the body is more or less sensitive?

A
  • higher threshold = less sensitive
  • need more stim to reach threshold ->more stim to be detected -> less sensitive
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10
Q

define: two-point limen/touch threshold

A
  • smallest separation of 2 points applied simultaneously to the skin that an still be discriminated
  • 2 point pain threshold = separation of 2 painful stim.
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11
Q

question: overall trend in detection threshold for body sensitivity?

A
  • most sensitive in face
  • less sensitive in leg and arms
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12
Q

question: over trend in discrimination threshold for body?

A
  • similar pattern to detection
  • less sensitive in legs
  • most sensitive in face
  • sensitive at fingertips
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13
Q

question: what factors influence two-point discrimination?

A
  • smaller mechanoreceptor field size
  • higher density of mechanoreceptors
  • want brain to receive 2 separate signals so need no overlap in recep. fields
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14
Q

question: what factors affect tactile sensitivity?

A
  • sex
    ⤷ fem. more sensitive
  • age
    ⤷ older = less sensitive (in general)
    ⤷ in blind = braille could be close together and older people could still recog.
  • genetics
    ⤷ identical twins = more similar tactile sensitive than fraternal
  • autism can -> hypersensitivity
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15
Q

question: what can promote touch adaptation?

A
  • larger stim. area
  • weaker intensity force
  • stim. less sensitive areas of body
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16
Q

explain: pathway for nociceptive signals

A
  • follows spinothalamic pathway
  • signals arrive at dorsal horn of spinal cord
  • interneurons in dorsal horn receive info from brain
    ⤷ cog. info (ex. emo.)
  • interneurons form synapses on neurons that convey nociceptive info to brain
17
Q

explain: gate control theory

A
  • pain signals can be blocked through feedback circuit in dorsal horn
  • inhibitory interneuron = gate
    ⤷ can reduce feeling of pain
    ⤷ A-alpha or A-delta fiber
  • relaxing beha. -> activating inhibitory interneuron -> blocks pain
18
Q

question: what areas process the discriminative vs emotional aspects of pain?

A
  • discriminative = thalamus, S1, S2
  • emotional
    ⤷ anterior cingulate cortex (reward anticipation, decision making. emo.)
    ⤷ insula (self awareness, emo., homeostatic emo.)
    ⤷ prefrontal cortex (cog. and executive control)
    ⤷ amygdala (emo. memory, fear)
19
Q

define: referred pain

A
  • pain arises in deeper structure of body is actually felt elsewhere
  • bc convergence of afferent fibers on spinal cord from diff. body parts
  • ex. heart attack
    ⤷ pain in arms/shoulders but actually from heart
20
Q

question: how is pain measured? (2)

A

1. univariate approach
- group all dimensions of pain together
- measure with standard psychophysical techniques (threshold)

2. multivariate approach
- separately asses different dimensions of pain
⤷ quality, intensity, location
- harder to gauge some bc feelings are subjective

21
Q

question: why do people have different pain thresholds?

A
  • biological factors
    ⤷ genetics
  • psychological factors
    ⤷ mood
  • social factors
    ⤷ economic
22
Q

question: what causes pain sensitization (increased sensitivity)?

A
  • peripheral and central changes
  • peripheral = interaction of recep. and inflammatory substances released after tissue damage
  • central = increased excitability of neurons at dorsal horn
23
Q

name + categorize: types of pain sensitization (3)

A

PERIPHERAL
- hyperalgesia
⤷ increased pain to normally painful stim.
- allodynia
⤷ normally innocuous (not harmful) stim. cause pain

CENTRAL
- neuropathic pain
⤷ chronic, intense pain hard to treat
⤷ nerve fibers are damaged and pain thresholds do not return to pre-injury lvls

24
Q

explain: phantom pain

A
  • lingering painful sensation in missing limb
  • pain pathways are still active without peripheral stim.
    ⤷ neurons where still stim. when amputated -> still painful
25
name: ways to treat and moderate pain (3)
**1. pharmalogical** - analgesics = dampen pain - anti-inflammatory = block inflammatory molecules that activate pain recep. - opiates = activate opiod recep. -> blocks pain sig. to brain **2. surgical and neurostimulatory** - removingparts or spinal cord or frontal lobe - TENS unit activates A-beta fibers ⤷ counterstimulation ⤷ activating tactile recep. -> activates inhibitory interneurons **3. psychological** - counterstim. or counterirritation - placebo effect ⤷ give drug w/ no actual effect but patients still claim it helps ⤷ may be due to endogenous opioids - relaxation, hypnosis, etc.
26
explain: itch receptors
- pruiriceptors - C fibers - spinothalamic system - activated by prurigenic chemicals like histamines - diff. from pain - sometimes itch also resp. to pain stim. bc interact in cord - pain can activate inhibitory > no itch
27
question: can scratching reduce itchiness?
- provides tactile stim. -> activates A-alpha or A-beta - at lvl of cord and/or brain - older people may strach more bc less merkel cells ⤷ less possibility to distract by scrating