Week 1 - Lecture 1 - Pain pathways and modulation Flashcards

1
Q

What is the ICF model?

A

International Classification of Functioning, Disability and Health

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2
Q

Identify the different components of the ICF model and explain each component.

A
  • BODY STRUCTURES – anatomical parts of the body
  • BODY FUNCTIONS – physiological functions of the body
  • IMPAIRMENTS – problems in body structure or function
  • ACTIVITY (limitations) – task or action at the level of the individual
  • PARTICIPATION (restrictions) – involvement in life situations
  • PERSONAL FACTORS – factors within a person
  • ENVIRONMENTAL FACTORS – physical, social, attitude
  • FUNCTIONING – the interaction among the components of the model that contribute to the overall ability to function (positive aspects)
  • DISABILITY – the interaction among the components of the model that limit the person’s ability to function (negative aspects)
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3
Q

Why study pain?

A
  • A primary reason for people to seek medical attention
  • Understand the physiology of pain for context or background
  • Understand the complexities of pain and how it has an impact on our patient’s lives
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4
Q

What is the function of pain?

A

• Informs the body when something is wrong • A survival mechanism
Pain: An unpleasant sensory and emotional
experience associated with actual or potential
tissue damage
(International Association for the Study of Pain)

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5
Q

How do we understand pain?

A

Something happens somewhere in the periphery, the signal goes to the brain, we process that signal and then there is a response (either physical or emotional)

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6
Q

What are the four main components of how we understand pain.

A

Four main components:
1- Transduction (physical injury - nerve response)
2- Transmission
3- Perception (understanding what is happening)
4- Modulation (Transitioning into chronic pain)

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7
Q

What composes the nervous system?

A
  • Central Nervous System : Brain and Spinal Cord
  • Peripheral Nervous System: Nerve fibers that are all over the body sending signals to the different tissues and to the CNS
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8
Q

What are the different types of receptors?

A
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9
Q

What has free nerve endings?

What has no receptors?

A

Free nerve endings :
Skin
Bone
Muscles

No receptors in:
Articular cartilage
Synovial membrane
Pericardium - tissue around the heart
Brain tissue

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10
Q

What is an electrical impulse in the nerve?

A
  • Action Potential: signals move along a nerve process (axon) as a wave of membrane depolarization (more negative)
  • Rapid transitions between negative and positive electrical potentials
  • The action potential moves along the axon to the nerve ending where it releases chemicals
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11
Q

The physiology of pain

A
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12
Q

What is an afferent pathway?

A

(ascending)

Carry message to the brain for interpretation

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13
Q

What is an efferent pathway?

A

(descending)

Carry messages from the brain via the spinal cord

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14
Q

What are nociceptors?

A
  • Receptors that activate the afferent pathways
  • Unevenly distributed in the muscles, tendons,
    subcutaneous tissue and the skin

NOCICEPTORS are sensitive and respond to noxious stimuli stimuli that can cause tissue damage or when tissue damage has taken place
• Response to extremes of mechanical, chemical and thermal stimuli • E.g., cuts, burns, sprains

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15
Q

What are the possible stimulus or sources of pain?

A

1- Mechanical - Poke, pinch, aggressive compression (ex: slip and fall)
2- Chemical - inflammatory mediators
3- Thermal - extreme heat or cold applied to tissue

  • Pain receptors are unable to adapt to repeated stimuli and thus continue to react until stimuli are removed. Ex: let’s say you are putting gas in the car, the smell of gas will kinda go away but that will not happen to pain receptors
  • When pain receptors are stimulated electrical impulses are transmitted to the spinal cord along wo afferent fibres
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16
Q

What is the general idea of a pain pathway?

A

• Impulses travel up the spinal cord to the brain

First point : transmission
Second point: perception
Third point: modulation

• In the brain, the cortex interprets the impulses as pain and identifies the location
and qualities of pain
• Endorphins and enkephalins, natural opioid-like substances • Block transmission of painful impulses to the brain

17
Q

What are the components of the pain pathway?

A
  1. Receptors
  2. Primary afferents, 1st order neurons
  3. Dorsal horn of the spinal cord
  4. Ascending fibers, 2nd order neurons
  5. Thalamus
  6. Cortex and other brain areas
18
Q

Explain a primary afferent.

What is the purple line?

What is the blue line?

What is the red line?

A

PRIMARY AFFERENTS (1st ORDER)

What is the purple line
A beta fibers
What is the blue line
A delta fibers
What is the red line
C fibers

19
Q

What are the different primary afferents and their respective sizes?

A

Ab fibers
sensory from cutaneous receptors, non-nociceptive and do not transmit pain
Ad and C fibers sensations of pain and temperature from peripheral nociceptors

20
Q

What is fast and slow pain?

A
  • A sharp first pain followed by a second dull, aching, longer lasting pain
  • First fast pain is transmitted by the myelinated A(delta) fibers
  • Second slow pain is transmitted by the unmyelinated C fibers
21
Q

What is the role of the spinal cord during transmission of signals to the brain?

A

The spinal cord is more than a junction area for transmission of signals to the brain. There are spinal neural circuits, which can alter signal transmission.

C fiber .. our bodies have these sort of safety mechanisms so that we aren’t in a painful stimulus all the time. = image on the right

Inhibition of the inhibitory neuron by the C fiber when there is pain = image on the left

22
Q

What is an ascending fiber of 2nd order?

A

• 2nd order neurons
• Nociceptive signals are sent to the spinal cord and then to different parts of the brain where sensation of pain is processed
• There are a pathways/regions for assessing the: • Location, intensity, and quality of the
noxious stimuli
• Unpleasantness and autonomic activation • E.g., fight/flight response, anxiety

80% of your 2nd order neurons = is in the spinothalamic tract = it carries most of our
2 main afferent pathways = spinothalamic tract + spinoreticular tract

23
Q

What is the role of the thalamus in the pain pathway?

A

General idea = Thalamus : accepts info and shoots it up to the rest of the brain (via third-order neurons)

  • The Thalamus is a relay station
  • 2nd order neurons synapse here
  • Sends signals (3rd order neurons) to higher brain regions
24
Q

Name a few examples of places in the brain where the thalamus is transmitting the signal?

A

Amygdala: fear response
Somatic sensory: location, type (hot cold sharp), quality of the pain
Insular cortex: emotional response of pain (sad)- based on the other aspects will respond

25
Q

Is the pain perception the same in everyone? Yes or no and explain why.

A
  • Objective and subjective aspects of injury and pain are DIFFERENT!
  • Despite similar injury, people can differ in how much pain they feel
  • Depending on the context, pain may not be felt despite injury
  • Suggests that a physiological mechanism controls the transmission of nociceptive signals to the brain or modifies the interpretation of pain
26
Q

What do you do when you think something painful is about to happen?

A

MODULATION

Flinch away from it
Tense up
Rubbing it

Why do we do that?

It’s maybe a distraction,
your changing some sensory input into your body (override that painful experience)

27
Q

What are the different models of pain experience?

A

Gate control theory
Blocking ascending pathway

Descending Pain Control
Expands on Gate Control theory with input from higher brain centers

Endogenous opioids
Nociceptors to stimulate the release of endorphins, bind to blobk pathway

28
Q

Explain the gate control theory.

A

The concept of the gate control theory is that non-painful input closes the gates to painful input
Ascending Aβ fibers block pain impulses at the spinal cord level carried along Aδ and C fibers
Results in prevention of the pain sensation from traveling to the central nervous system

***

Inhibitory neuron = Little yellow i = is always on and is making sure that the non-painful input closes the gates to painful input

A-beta neuron = L in green

Large fiber travels faster than a small fiber = which allows to essentially

29
Q

What is the difference between a large diameter and a small diameter fiber? What happens if they are myelinated or unmyelinated?

A

(L) Large diameter, myelinated (fast– can beat pain)

  • Stimulates projection cell (P)
  • Stimulates inhibitory neuron (i)

(S) Small diameter, myelinated/unmyelinated (pain)

  • Stimulates projection cell (P)
  • Inhibits Inhibitory neuron (i)

• Occurs whether or not signal reaches brain (top) • E.g., rub thumb after hitting it with a hammer

30
Q

What is the descending pain control?

A
  • Activity from descending fibers (e.g., PAG) project to the dorsal horn and could also modulate this gate (inhibit/facilitate)
  • Nociceptive information reaches a threshold that exceeds the inhibition elicited
  • It “opens the gate” and activates pathways that lead to the experience of pain and its related behaviors.

***Trying to block the signal in getting to that second order neuron, in addition to the gate control theory

Inhibition of the signal but the signal continues and is too strong (and we can’t override it), it can override the descending pathways and that reenforces the urge to, for example, move your hand

Abnormality in this system can lead to chronic pain : the pain is not inhibited. Lots of different ways that can happen

31
Q

What is the endogenous opioids theory?

A

• The brain releases endogenous opioids in response to pain perception
• Internally produced molecules with opioid-like action to regulate transmission of
nociceptive signals
• Similar brain regions that modulate the signal from nociceptive afferents
• Distribution varies by endogenous opioid family

32
Q

What are the three classes of the molecules of endogenous opioids that have been identified?

A

Three classes:
Enkephalins
Endorphins
Dynorphins
Produced by the same brain regions and that there are these 3 classes that exist = is what you need to know

Don’t have to know the details, how they function or where they come from

33
Q

How do the endogenous opioids function?

A

• Inhibitory effect on nociception
• Slower but has a longer lasting effect
• We naturally express the receptors for these molecules thus allowing the chemical to
bind for a long period of time
• Relies on circulation of chemical versus action potential along neurons • E.g., prescribe ROM (within a pain free range)

***Bad circulation = these will not function as well, because they won’t get to the root of the problem(increasing circulation = better)
Prescribing simple ROM (range of motion)= will increase blood flow and also increase the release of those natural opioids

34
Q

What is the Neuromatrix theory of pain?

A

Melzack’s: pain experience

Neuromatrix theory:
Motivational Affective = like the unpleasant of it
Cognitive Evaluative = has to do more with the cognitive state, perhaps different cultural views, is the pain perceived as good or bad
Sensory Discriminative = physiological characteristics of the pain