Pain and analgesics second half of 1 2.0 Flashcards

1
Q

Where does the AP go after it has gone through the first synapse in the spinal cord?

A

Crosses over to the other side of the body and goes up into the brain, into the thalamus

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2
Q

What type of input can the somatosensory part of the cortex receive?

A

Touch and nociception

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3
Q

What does the somatosensory cortex do with the touch and nociception?

A

Tells the brain where it has come from

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4
Q

Role of insular and anterior cingulate cortex in nociception?

A

Tells the brain that it is pain that is being experienced, affect your mood

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5
Q

How is the body mapped regarding pain perception and location?

A

As you go round the outside of the somatosensory cortex, different parts of it receive input form different body areas

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6
Q

What is the pain pathway to the brain?

A

Spinothalamic pathway/tract

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7
Q

Why is pain referred?

A

Not enough space in somatosensory cortex to have an acute sensation to map every part of the bodys pain

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8
Q

Which body parts have a good pain mapping (know where the pain is coming from)?

A

Skin

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9
Q

Which body parts have a poor pain mapping (don’t know where the pain is coming from)?

A

Internal organs

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10
Q

Where does pain sourced in the oesophagus feel like its coming from?

A

Heart

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11
Q

What can hurt when having a heart attack?

A

Left arm

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12
Q

Which neurons are shared in referred pain?

A

Second order

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13
Q

What is the second order neuron?

A

The one after the first synapse in the spinal cord

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14
Q

What is hyperalgesia?

A

Increased response to a noxious stimulus

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15
Q

What is allodynia?

A

Painful responses to a non-noxious stimulus

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16
Q

Why is hyperalgesia a thing?

A

To protect already injured/damaged areas of the body

17
Q

How does nociceptor sensitisation work?

A

Cut skin–> skin cells break–> intracellular components of skin cells is released into extracellular space–> some of these components are H+, ATP, K+ which are nociceptor agonists

18
Q

Why does an elevated conc of extracellular K+ increase the amount of APs fired from a neuron?

A

Conc grad is disrupted meaning it is harder for the neurons to repolarise, makes them more excitable

19
Q

What is unusual about nociceptive neurons?

A

They can release NTs from their dendritic end

20
Q

Which NT is released from the dendritic end of nociceptive neurons?

A

Substance P

21
Q

What does substance P do to blood vessels?

A

Activate receptors on blood vessels that makes them leaky

22
Q

Outcome of substance P’s action on blood vessels?

A

More nociceptor agonists are released, generating more nociceptive APs

23
Q

Which cells does substance P recruit?

A

Mast cells

24
Q

Action of mast cells?

A

Release histamine which makes blood vessels leaky

25
Q

Which three molecules are used for healing the part of the body that has been damaged?

A

Bradykinin, prostagladin, neural growth factor

26
Q

What does nerve growth factor do?

A

Activates TrkA receptor–> this sensitises nociceptors by lowering their opening threshold

27
Q

What is peripheral sensitization?

A

Increased sensitivity of peripheral nociceptors

28
Q

What is central sensitization?

A

Increased transmission in spinal cord

29
Q

Which fibres do itch sensations travel down?

A

Adelta and C

30
Q

Difference between pain and itch?

A

Analgesics don’t inhibit itch, can imagine an itchy sensation but not a painful one

31
Q

What kind of input cures an itch?

A

Nociceptive (scratching it hard)