MVC - Nerve Fibres in Nociception Flashcards

1
Q

What can cause action potentials in free nerve endings?

A

Activation of ion channels if sufficient depolarisation occurs

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2
Q

What are some features of A-delta fibres? (5)

A

Mechanosensitive or mechanothermal nociceptors (mechanical and thermal)

  • Myelinated
  • Myelin (Shwann cells) insulates/protects/nourishes fibre
  • Rapid/saltatory conduction (sharp well localised pain). 5-40m/s

Respond to first pain

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3
Q

What are some features of C fibres? (4)

A

Polymodal nociceptors (mechanical, thermal and chemical)

  • Unmyelinated
  • Dull/aching pain. Slower 0.5-2m/s

Respond to second pain

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4
Q

What are the features of nociceptors? (2)

A
  • Small diameter
  • Slowly conducting (Ad,C), compared with other sensory fibres
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5
Q

How are harmful stimuli detected?

A

Transcutaneous recordings using microneurography show that there are specialised nerve fibres that detect noxious stimulation

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6
Q

Are pain signals directed to a single “pain center” in the brain?

A

No

  • Pain signals are integrated from different brain structures into a conscious experience of pain
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7
Q

Discriminative component vs Affective-motivational component

A

The discriminative component:

  • Pathways that target the traditional somatosensory areas of cortex,

The affective-motivational component

  • Depends on additional cortical and brainstem pathways. (Paleospinothalamic)
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8
Q

What are the components of the nociceptive ascending systems? (2)

A

Body (and posterior portion of the head)
Pain and temperature:

  • Spinothalamic tract a.k.a. anterolateral system

Face (and anterior portion of the head)
Pain and temperature:

  • Trigeminothalamic tract (face, oral)
  • Through the spinal nucleous of the trigeminal complex
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9
Q

What are 3 examples of painkiller types?

A

Painkillers: insight into pain modulation

1) Local anaesthetic, also known as nerve block
eg. lidocaine, novocain

  • Inhibit sodium channel molecules directly and prevents the generation and propagation of action potentials

2) Non-steroidal anti-inflammatory drugs (NSAIDs)
Paracetamol

  • Target the production of prostaglandins by inhibiting the enzyme COX

3) Opioid analgesics
Ketamine

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10
Q

What are
Inflammatory chemicals/mediators and 3 examples of them?

A

Cause an increase in Neuronal Excitability

  • Prostaglandins
  • Bradykinin
  • Substance P
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11
Q

How do sunburn nociceptors function?

A

Sunburn Nociceptors are bathed in inflammatory mediators
→ Increase sensitivity of nociceptors
→ Lower the depolarisation threshold

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12
Q

What is the first level of modulation in the processing of nociceptive signals?

A

Dorsal root of the spinal cord

Segmental controls of spinal origin:

  • A gating mechanism in the spinal cord (substantia gelatinosa of dorsal horn) can be opened or closed in varying degrees thereby modulating incoming signals before they reach the brain
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13
Q

How could a first pain mask a second pain?

A

Descending pathways diffuse inhibitory controls induced by nociceptive stimuli

  • Ascending nociceptors make connections within the brainstem, e.g. in the periaqueductal gray matter.
  • These brain stem structures can return descending signals to inhibit nociceptors.
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14
Q

What controls acute stress?

A

Descending controls of the brain associated with psychological factors

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15
Q

How does inhibition by enkephalin work?

A

Pre-synaptically

  • Makes the action potential narrower → limits neurotransmitter release

Post-synaptically

  • Generates an inhibitory postsynaptic potential driving the cell away from the action potential firing threshold
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16
Q

What is referred pain?

A

Pain perceived at a location other than the site of nociception

  • Very few projection neurons specialised for transmission of visceral pain.
  • Cutaneous and visceral nociceptive afferents converge on projection neurons
17
Q

Pain as disease: Allodynia and Neuropathic pain

A

Allodynia

  • Pain due to a stimulus that does not normally provoke pain.

Neuropathic pain

  • Pain caused by a lesion or disease of the somatosensory nervous system