Case 2 - Modulation of the Perception of Pain Flashcards

1
Q

what is the gate control theory of pain

A

is a mechanism, in the spinal cord, in which pain signals can be sent up to the brain to be processed to accentuate the possible perceived pain, or attenuate it at the spinal cord itself

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2
Q

what is the gate

A

the mechanism where pain signals can be let though or restricted

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3
Q

what happens if the gate is open

A

pain signals can pass through and will be sent to the pain or perceive the pain

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4
Q

what happens if the gate is closed

A

pain signals will be restricted from travelling up to the brain and the sensation of pain won’t be perceived.

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5
Q

diagram showing the gate control theory of pain

A
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6
Q

where is the pain gate mechanism located

A

in the dorsal horn of the spinal cord, specifically in the substantia gelatinousa

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7
Q

what are the interneurones

A

the interneurones within the substantia gelatinosa are what synapse to the primary afferent neurones, and are where the gate mechanism occurs.

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8
Q

what does the substantia gelatinosa do

A

modulates the sensory information that is coming in from the primary afferent neurones

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9
Q

what are the three different types of primary afferent neurones

A
  • A-beta fibres
  • A-delta fibres
  • C fibres
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10
Q

describe A-beta fibres

A

large diameter fibres, have quick transmission of impulses, due to their myelination - these type of fibres are activated by non-noxious stimuli, such as light, touch, pressure and hair movement

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11
Q

describe A-delta fibres

A

a smaller diameter fibre - they are thinly myelinated and are stimulated by noxious stimuli, such as pain and temperature, specially sharp, intense tingling sensation

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12
Q

descrie C fibres

A

have the slowest transmission of impulse since they are not my elated. these type of fibres are activated by pain and temperature, namely prolonged burning sensations

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13
Q

what happens if the interneurones in the SG are stimulated by the non-noxious A beta fibres

A

an inhibitory response is produced and there are no pain signals sent to the brain, and in this instance the ‘pain gate’ is closed.

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14
Q

what happens if the interneurones are stimulated by the smalller diameter A delta or C fibres

A

an excitatory response is produced. in this case, pain signals are sent to the brain, these can be modulated, sent back down through descending modulation and perceived as varying amounts of pain

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15
Q

what can the activation of the large diameter A beta fibres do

A

can help reduce and inhibit the transmission of the small diameter A delta and C fibres

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16
Q

what happens at the spinal cord

A

the primary afferent neurones come from the periphery and synapse with the second order neurones

17
Q

where does this happen?

A

the dorsal horn of the spinal cord

18
Q

what are the possible neurotransmitter or neuropeptides that can be released

A
  • glutamate
  • glycine and GABA
  • substance P
  • endorphins and serotonin
19
Q

what happens when glutamate is released

A

it is excitatory. the activation of the NMDA receptors by glutamate increase receptive field size, decreases activation threshold and extends depolarisation which leads to activation of the dorsal horn neurones

20
Q

what happens when glycine and GABA are released

A

they are inhibitory. Glycine can bind onto NMDA, while GABA has its own specific receptors

21
Q

what happens when substance P is released

A

it is an excitatory neuropeptide. these are found in respond to tissue damage by causing vasodilation, inflammation or pain

22
Q

where is substance p found

A

C fibres

23
Q

where do endorphins and serotonin get released

A

into the descending pathway to also help with gate control and the modulation of pain

24
Q

what are the two types of second order neurones

A
  • wide dynamic range (WDR)
  • nociceptive specific range neurones (NS)
25
Q

where do the WDR neurones synapse tp

A

the A beta, A delta and C fibres

26
Q

what are WDR neurones activated by

A

noxious and non noxious stimuli

27
Q

where do the NS neurones synapse to

A

a delta and C fibres

28
Q

what are the NS neurones activated by

A

noxious stimuli only

29
Q

describe the third order neurones

A

they are located in the brain stem and diacephalon, they transmit the pain signal to the cerebral cortex, where the pain signal, from the a delta or c fibres can be further modulated.

30
Q

mechanism of action of the TENS

A
  • activates the pain gate mechanism to inhibit pain signals going up to the brain, thus reducing the sensation of pain.
  • activates non-noxious afferent fibres, which in turn activates the ‘pain-inhibiting’ interneurones in the spina cord, and thus minimises perceived pain as an output
31
Q

why does this happen?

A

because TENS can activate a beta fibres, which helps facilitate the gate control mechanism. the activation of the a beta fibres will inhibit the input from the noxious a delta and c fibres

32
Q

what does the interferential current (IFC) modality do

A

inhibits pain through the gate control mechanism, and other neural mechanisms