Week 2 Flashcards

1
Q

What are sensory afferent fibres involved in?

A

The process of nociception

Sensory afferent fibres play a critical role in transmitting pain signals to the central nervous system.

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2
Q

What is the anatomy and function of the dorsal horn?

A

It is the site where primary afferent fibres synapse with second-order neurons and where excitatory/inhibitory interneurons interact

The dorsal horn is crucial for pain modulation.

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3
Q

What are the ascending and descending pathways associated with?

A

Nociceptive regulation

These pathways help in the transmission and modulation of pain signals.

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4
Q

What clinical signs indicate primary nociceptive somatic pain?

A

Signs include localized pain, pain that is consistent, and pain that reproduces with mechanical movement

Recognizing these signs is important for accurate assessment.

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5
Q

What is acute nociceptive pain?

A

Pain that arises from actual or potential tissue damage and has a protective role

It evokes a painful sensation that draws immediate attention.

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6
Q

How can observing someone else get injured elicit a pain response?

A

Through mirror neurons and empathetic responses

This phenomenon illustrates the social and psychological aspects of pain perception.

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7
Q

What is the first step in the clinical reasoning process?

A

Determine if the patient is appropriate for physiotherapy or if other medical conditions need to be ruled out

This step is essential for ensuring patient safety.

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8
Q

What question should be asked to assess if pain fits a mechanical framework?

A

Does moving a certain way reproduce their pain?

This helps in understanding the nature of the pain.

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9
Q

What distinguishes peripheral pain mechanisms from supraspinal pain mechanisms?

A

Peripheral pain mechanisms are bottom-up, while supraspinal pain mechanisms are top-down

Pain is always a combination of both mechanisms.

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10
Q

What happens to pain perception over time after an injury?

A

The relationship between tissue damage and pain weakens beyond normal healing time

Central sensitization may occur, leading to persistent pain.

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11
Q

What are nociceptors?

A

Specialized neurons that detect and respond to potentially damaging forms of energy

They play a key role in the sensation of pain.

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12
Q

What is sensory transduction?

A

The process by which harmful energy is converted into ionic currents

This process is essential for the activation of nociceptors.

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13
Q

How are nociceptors classified?

A

Based on receptor type and fibre characteristics

This classification helps in understanding their function and response.

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14
Q

Fill in the blank: Nociceptors have a _______ threshold to generate an action potential.

A

high

This means a higher intensity stimulus is required for activation.

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15
Q

What neurotransmitters are released by calcium channels from 1st order neurons in the dorsal horn?

A
  • Glutamate
  • Substance P
  • Calcitonin gene-related peptide (CGRP)

These neurotransmitters are crucial for excitatory signaling.

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16
Q

What areas of the brain are involved in pain perception?

A
  • Premotor/Motor Cortex
  • Cingulate Cortex
  • Prefrontal Cortex
  • Amygdala
  • Sensory Cortex
  • Hypothalamus/Thalamus
  • Cerebellum
  • Hippocampus
  • Spinal Cord

These areas form a distributed network for processing pain.

17
Q

What role does the amygdala play in pain perception?

A

It modulates pain perception through connections with the descending pain inhibitory system

This is important when considering the impact of fear and learning on pain.

18
Q

What is the function of the periaqueductal gray?

A

Involved in both ascending and descending pain modulation systems

It plays a key role in the body’s pain response.

19
Q

What does stress affect regarding pain perception?

A

It alters homeostasis and can influence pain perception in both acute and chronic settings

Acute stress can alert individuals to dangerous situations.

20
Q

Triage

A

the first person that talks to you and asks dos the patient belong in the clinic?

21
Q

Basic nerve function
Action potential

A

Na+ channels open, Na+ enters cell (sodium)–> K+ channels open, Na+ enters cell, Na+ channel closes and no more Na+ enters cell–> K+ leaves cell causing membrane potential to resting level–> K+ channel closes

22
Q

Is it peripheral driver or supra-spinal (central) driver? location, quality, intensity, behaviour, duration, clinical signs

Pain symptoms

A

Peripheral:
location: Precise
Quality: sharp, blunt, dull, aching
intensity: worse with movement
behaviour: does not spread
duration: eased quickly with rest
clinical signs: associated with an injury

Supra:
L: shifts and jumps around
Q: unusual
I: severe
B: unpredicatable
D: does not ease quickly
C: pain not associated (e.g standing at bust stop hurts, but standing at party is fine)

23
Q

If the pain is peripheral somatic nociceptive pain. starts off at physiological stimuli, explain rest

A

Nociceptor–> drosal root ganglia> spinal cord->thalamus>
Brain goes what will we do and have we experienced this before?

24
Q

3 types of physiological stimuli

A

mechanical (pinprick)
thermal (heat/cold)
chemical injury

25
Peripheral and central sensitisation (amplification)
Peripheral sensitisation occurs at the site of injury or inflammation. The affected nerves become more responsive, making normally mild stimuli feel more painful. Example: A sunburn making light touch feel like burning pain. Central sensitisation happens in the spinal cord and brain. The nervous system becomes overly reactive, amplifying pain signals even when the injury has healed. This can cause widespread or long-lasting pain. Example: Chronic pain conditions like fibromyalgia, where even gentle touch can be painfu
26
characteristics of primary afferent fibres
AB fibres (fast, large, highly myelinated)-> fast initial messenger A delta (small, thin myalination, medium speed)-> localised pain C fibres (smallest, unmyelinated, slow)-> slow messenger to process better
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Cutaneous mechanoreceptors
touch receptors in the skin
28
Nociceptors fibres (AB, A delta, C go where?)
Aβ (A-beta) fibers → Normally carry touch and vibration signals. They go to laminae III & IV (but can sprout into lamina II in chronic pain, causing allodynia). Aδ (A-delta) fibers → Carry sharp, fast pain and temperature signals. They go to lamina I & V. C fibers → Carry slow, dull, burning pain signals. They go to lamina I & II (especially the substantia gelatinosa in lamina II).
29
Ascending Pathways (Pain Signals Traveling Up) Spinal and Supraspinal Pathways of nociception
Spinothalamic Tract (Red): * One of the main pathways that transmits pain and temperature signals from the spinal cord to the thalamus, which then relays the information to the higher brain centers for pain perception. This pathway is involved in the conscious perception of pain. Spinobulbar & Parabrachial Pathways (Blue): * These pathways send pain-related information to regions like the amygdala and hypothalamus, which regulate emotional and autonomic responses to pain. The amygdala is particularly important for the emotional aspect of pain (fear, stress, anxiety).
30
Descending pathway (Spinal and Supraspinal Pathways of nociception)
Periaqueductal Gray (PAG): * A key area in the brainstem that helps suppress pain by activating descending pain modulation pathways. Sends signals to areas like the locus coeruleus and rostroventromedial medulla (RVM), which release neurotransmitters that inhibit pain at the spinal level. * Descending Monoaminergic Controls: These pathways help regulate pain perception by reducing pain signals before they reach the brain.
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