Sensory systems (including physiology of pain) Flashcards

1
Q

what are different types of sensory information associated with

A

specific receptor types responding to a specific sensory modality

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2
Q

give some examples of specific receptors

A

mechanoreceptors, chemoreceptors, thermoreceptors, nociceptors, proprioceptors

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3
Q

what is the receptive field of a receptor

A

the area in which they respond to a stimulus

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4
Q

what are the different types of receptor structures

A

can be free nerve endings e.g. nociceptors

can be complex structures e.g. pacinian corpuscle, meissners corpuscle

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5
Q

list some receptor structures and what stimuli they respond to

A
  1. tactile meissners corpuscle - light tough
  2. tactile merkles corpuscle - touch
  3. free nerve ending - pain
  4. lamellated pacinian corpuscle - deep pressure
  5. ruffini corpuscle - warmth
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6
Q

what do all sensory receptors do the their adequate stimulus

A

transduce it into a depolarisation (the receptor generator potential)

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7
Q

what determines the size of the receptor generator potential

A

the intensity of stimulus

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8
Q

what does the receptor generator potential evoke

A

firing of APs for long distance transmission

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9
Q

what determines the frequency and duration of APs fired

A

the intensity of stimulus

porportionally

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10
Q

what does the receptive field encode

A

the location of the action potential

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11
Q

what determines neurotransmitter release

A

the pattern of action potentials arriving at the axon terminal

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12
Q

briefly summaries the steps in signal transduction

A
  1. stimulus
  2. transduction site = receptro generator potential
  3. trigger zone - receptor potential integrated
  4. myelinated axon - firing of APs - frequency and duration based on stimulus
  5. axon terminal - neurotransmitter release in response to AP
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13
Q

what determines acuity

A

density of innervation and size of receptive fields

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14
Q

what transmits action potentials to the CNS

A

axons

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15
Q

what 2 types of primary afferent fibres mediate proprioception

A

mechanoreceptive:

Aα & Aβ

eg muscle spindles, golgi tendon organs etc

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16
Q

what 3 types of primary afferent fibres mediate cutaneous sensation

A

thermoreceptive and nociceptive:

Aβ = large myelinated (30-70m/s) touch, pressure, vibration

Aδ = small myelinated (5-30m/s) cold, “fast” pain, pressure

C = unmyelinated fibres (0.5-2m/s) warmth, “slow” pain

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17
Q

where do all the primary afferent fibres enter the spinal cord

A

at the dorsal root ganglion

or cranial ganglia for the head

18
Q

what do Abeta fibres mediate

A

touch pressure, vibration

19
Q

what do Adelta fibres mediate

A

cold, fast pain, pressure

20
Q

what do C fibres mediate

A

warmth, slow pain

21
Q

what is the route of transmission of Aa, Ab fibres

A

project straight up through ipsilateral dorsal columns

synapse in cuneate & gracile nuclei

the 2nd order fibres cross over midline (decussate) in the brain stem & project to reticular formation, thalamus and cortex

22
Q

what is the route of transmission of Adelta and C fibres

A

synapse in the dorsal horn

the 2nd order fibres cross over the midline in the spinal cord

project up through the contralateral spinothalamic (anterolateral) tract to reticular formation, thalamus and cortex

23
Q

what does the different pathways for transmission of sensory information explain

A

explains consequences of different spinal cord injuries

24
Q

what does damage to the dorsal column cause

A

causes loss of touch, vibration, proprioception below lesion on ipsilateral side

25
Q

what does damage to the anterolateral quadrant cause

A

causes loss of nociceptive & temperature sensation below lesion on contralateral side

26
Q

where is the ultimate termination of the sensory fibres pathway

A

somatosensory corted (S1) of the post central gyrus

27
Q

what produces the sensory homunculus

A

extent of representation - related to the density of receptors in each location

28
Q

what are the three processes in sensory pathways

A

adaptation
covergence
lateral inhibition

29
Q

what is adaptation

A

the change over time in the responsiveness of the sensory system to a constant stimulus

30
Q

what is convergence

A

when non-specific ascending pathways combine e.g. touch and temperature responses so that there is one larger group of info arriving in the brain

reduces acuity and may underlie referred pain

31
Q

what is lateral inhibition

A

when activation of one sensory input causes synaptic inhibition of tis neighbours

gives better definition of boundaries - cleans up sensory information

enhances the perception of the stimulus

32
Q

list some examples of different types of pain

A

sharp, stabbing vs diffuse, throbbing pain

fast (initial) pain vs slow (delayed) pain

acute vs chronic pain

visceral pain

referred pain

phantom limb pain

33
Q

what activate signal transduction in nociceptors

A

low pH, heat

local chemical mediators (e.g. bradykinin, histamine, prostaglandins)

34
Q

how does pressure alleviate pain

A

gate control theory:

  • pressure activates Aa/b fibres
  • activate inhibitory interneurones
  • interneurons release opioid peptides (endorphins)
  • endorphins inhibit transmitter relase from Adelta/C fibres
    = CLOSE THE GATE OF PAIN

happens at the segmental level

35
Q

how does the gate control theory work in the descending controls

A

same inhibitory interneurones are also cite by descending pathways from the peri-aqueductal grey matter and nuclus raphe magnus - also close the gate

activated by opiates

36
Q

what do prostaglandins do to nociceptors

A

sensitise them to bradykinin

37
Q

how do NSAIDS work as an analgesic

A

they inhibit cyclo-oxygenase which converts arachidonic acid to prostaglandins

they are also anti-inflammatory so work well with pain associated with inflammation

38
Q

how does local anaesthetics block pain

A

block Na+ action potential and therefore all axonal transmission

39
Q

how do opiates e.g. morphine work as an analgesic

A

reduce sensitivity to nociceptors

block transmitter release from the dorsal horn (hence epidural administration)

activate descending inhibitory pathways

40
Q

what is TENS

A

trans cutaneous electric nerve stimulation