Tutorial 2- Somatosensation Flashcards

1
Q

In the skin, sensation of touch is mediated by

A

cutaneous mechanoreceptors

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2
Q

maintained skin stretch is mediated by

A

ruffini endings

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3
Q

continuous pressure is sensed by

A

merkel disk receptors

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4
Q

vibration is sensed by

A

pacinian corpuscles

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5
Q

the nerve fibres that transmit touch info are mainly

A

A beta fibres

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6
Q

are there different thermoreceptors for each level of temperature?

A

yes

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7
Q

painful stimuli are mediated by

A

nociceptors

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8
Q

temperature and painful stimuli are transmitted by axons of

A

A delta and C fibres

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9
Q

pain is not a stimulus, rather

A

ex extreme cold is a stimulus

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10
Q

c fibres can respond to many simuli, such as

A

chemicals, temperature (warmth and cooling) and itch - it is therefore polymodal

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11
Q

sensory nerves respond to increasing stimulus intensity by

A

increasing firing frequency proportionately with strength of stimulus

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12
Q

nerves that are stimulated by inflammation/mechanical damage:

A

nociceptors

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13
Q

A alpha receptors are not involved in cutaneous touch, rather in

A

deep joint proprioception- therefore only present in DRGs involved in deep joint proprioception

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14
Q

are c fibres myelinated or unmyelinated?

A

unmyelinated

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15
Q

diameter, speed and detectable stimuli for c fibres:

A

0.2-1.5 microm, 0.5-2 m/s, pain+temp.+itch

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16
Q

diameter, speed and detectable stimuli for A delta fibres:

A

1-5 microm, 5-35 m/s, pain+temp.

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17
Q

diameter, speed and detectable stimuli for A beta fibres:

A

6-12 microm, 35-75 m/s, touch

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18
Q

diameter, speed and detectable stimuli for A alpha fibres:

A

13-20 microm, 8-120 m/s, proprioception

19
Q

which NT do C, A delta and A beta fibres use?

A

glutamate

20
Q

in addition to glutamate, which other NTs can C fibres use?

A

peptidergic transmitters such as substance P and CGRP

21
Q

what do the differences in NT of c fibres do?

A

create 2 classes of c fibre, one which only uses glutamate and the other that uses both glutamate and peptidergic transmitters

22
Q

the touch pathway can also be referred to as the

A

medial lemniscal, dorsal column pathway

23
Q

where does the touch pathway cross the midline?

A

at the dorsal column nuclei in the medulla

24
Q

the nociceptive pathway is also referred to as the

A

spinothalamic/ anterolateral tract

25
Q

the nociceptive pathway crosses the midline

A

at the level of the spinal cord that it enters via a projection neuron, then doesn’t synapse again until the thalamus

26
Q

the touch and nociceptive pathways travel from the thalamus to the cerebral cortex via the

A

internal capsule

27
Q

does the brain receive both touch and nociceptive signals from the opposite side of the body?

A

yes

28
Q

do the touch, temp. and nociceptive pathways from body have equivalent pathways subserving the head and neck/

A

yes

29
Q

what are the names of the 3 pathways subserving the head and neck?

A
  1. Spinothalamic
  2. Trigeminal nerve
  3. Dorsal column/medial lemniscus—> divided into fasciculus gracilus and fasiculus cuneatus
30
Q

what does the spinothalamic transmit?

A

body pain

31
Q

what does the trigeminal nerve transmit?

A

face and neck pain

32
Q

where are the cell bodies of trigeminal nerve?

A

the trigeminal ganglion, which is analogous to the DRG

33
Q

how many branches are in the DRG?

A

2, 1 to organ and one to spinal cord

34
Q

which DRG is the fasciculus gracilus from?

A

the lumbar DRG

35
Q

which DRG is the fasciculus cuneatus from?

A

the cervical DRG

36
Q

which DRG does the trigeminal go via?

A

the rostral DRG

37
Q

which stimuli does the trigeminal nerve transmit?

A

all senses, so both nociception and touch

38
Q

what are local anaesthetics and how do they work/

A

membrane stabilising drugs, work by blocking sodium channels so no influx of sodium so no pain

39
Q

how do opioid painkillers work?

A

by acting on opioid receptors: delta, kappa and most importantly mew.

40
Q

what are the 3 main side effects of opioids?

A

constipation, decreased respiration, addiction

41
Q

how do NSAIDs work as painkillers?

A

they inhibit COX enzymes, which would normally produce prostaglandins which sensitize nociceptors

42
Q

TENS can be used to control certain chronic pain states by:

A

inhibiting interneurons and therefore utilising the gate theory, although mechanism is debatable

43
Q

what is the main theory of why electrodes permanently implanted into the PAG work? (ex in parkinsonian pain)

A

PAG is the pain centre, so this would stimulate descending pathways and signal to projection neurons in the spine, therefore “dumping” he NTs serotonin and NA onto the projection neurons which act as inhibitors and stop pain signals from c fibres reaching the brain.