Neurology 7 - Sensory Pathways Flashcards

1
Q

What is the somatosensory cortexes function?

A
  • The ability to interpret body sensations

- Mechanical, thermal, proprioceptive and nociceptive (not necessarily painful)

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2
Q

What does the function of mechanoreceptors depend on?

A
  • Degree of specialisation (from free nerve endings to elaborate accessory structures)
  • Location (in layers of skin, around hair shaft, in muscles and tendons)
  • Physiological properties (activation threshold determines sensitivity (low threshold)
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3
Q

What is nociception?

A
  • Provides information about unpleasant or harmful stimuli
  • When this information is processed by the brain it is percieved as pain
  • It can be measured
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4
Q

How is visceral pain transmitted?

A
  • Carried peripherally by autonomic nerves, and centrally in the spinothalamic and dorsal columns pathways
  • Localisation is mainly referred to the body wall at the same spinal level
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5
Q

How is somatic pain and termperature information transmitted?

A

Carried to the brain by the spinothalamic tract

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6
Q

List the characteristics of receptors involved in nociception

A
  • Polymodal (mechanical, thermal or chemical stimulus)
  • Free nerve endings
  • High threshold
  • Slow adapting (continue to fire impulses as long as the stimulus is present)
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7
Q

What is the function of taking information via the spinothalamic tract to the somatosensory I and II cortex?

A

Analysis of localisation and intensity of the noxious stimulus

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8
Q

What is the function of taking information via the spinothalamic tract to the forebrain?

A

Perception of pain

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9
Q

What is the function of taking information via the spinothalamic tract to the midbrain?

A

Inhibit pain

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10
Q

Where do the axons of the spinothalamic tract send collateral branches to?

A
  • Brainstem (reticular formation)
  • Thalamus (intralaminar nuclei)
  • Hypothalamus and some cortex
  • This triggers an increase in awareness and registers the unpleasantness of the stimulus
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11
Q

Describe central inhibition

A
  • Descending pathway in the brainstem is triggered which inhibits the nociceptive pathway in the dorsal horn
  • Pathway uses endogenous opiods and other transmitters
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12
Q

Describe the consequences of nociceptive dysfunction

A
  • Reduced pain but disposed to increased injury

- Some changes may exacerbate pain (eg. windup in dorsal horn, thalamic syndrome and phantom pain)

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13
Q

List and define the major somatosensory modalities

A
  • Touch (detection of light mechanical stimuli)
  • Thermosensation (temperature)
  • Nociception (noxious or potentially damaging stimuli)
  • Proprioception (mechanical displacement of muscles and joints)
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14
Q

Where are free nerve endings used?

A

Thermoreceptors and nociceptors

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15
Q

Where are enclosed nerve endings used?

A

Mechanoreceptors

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16
Q

Describe the classification of sensory neurons.

A
  • A beta are largest and fastest (mechanoreceptors of skin, touch and proprioception)
  • A delta are middle size and middle speed, they convey pain and temperature
  • C fibres are small and unmyelinated and therefore slow (temperature, pain and itch)
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17
Q

Define the term receptor

A

Transducers that convert energy from the environment into electrical stimulus

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18
Q

What type of fibres are used by thermoreceptors?

A
  • A delta and C-fibres
  • Free nerve endings
  • TRP (transient receptor potential) ion channels - heat activated TRPV 1-4, cold activated TRPM8 and TRPA1
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19
Q

List the types of mechanoreceptors and their use

A
  • Meissners corpuscle (fine discriminative touch, low frequency vibration - phasic)
  • Merkel cells (light touch and superficial pressure - tonic)
  • Pacinian corpuscle (deep pressure, high frequency vibration and tickling - phasic)
  • Ruffini endings (continuous pressure or touch and stretch - tonic)
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20
Q

Define stimulus threshold

A

A threshold is the point of intensity at which the person can just detect the presence of a stimulus 50% of the time (absolute threshold)

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21
Q

Define stimulus intensity

A

Increase strength and duration of stimulus results in increased neurotransmitter release and greater frequency of action potential

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22
Q

What is the function of tonic receptors?

A
  • Detect continuous stimulus strength
  • Transmit impulses to the brain as long as the stimulus is present
  • Keeps the brain informed of the status of the body (eg. Merkel cells, which slowly adapt)
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23
Q

What is the function of phasic receptors?

A
  • Detect changes in stimulus strength
  • Transmit impulses at the start and end of the stimulus - adapt quickly, fade in the middle
  • Eg. Pacinian corpuscle, sudden pressure excites the receptor and transmits a signal again when the pressure is released.
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24
Q

Compare the receptive fields of the arm, fingers and back

A
  • Arm has small receptive fields to allow detection of fine detail
  • Fingers have densely packed mechanoreceptors with small receptive fields
  • Large receptive fields allow the cell to detect changes over a wider area, less precise
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25
Q

Define receptive field

A

The receptive field is the region on the skin which causes activation of a single sensory neuron when activated

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26
Q

What is two point discrimination?

A
  • Minimum distance at which two points are percieved as separate
  • Related to the size of a receptive field (whether you can feel two points or one)
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27
Q

List the important dermatomes to remember

A
  • C5 is the clavicle level
  • C6 down the thumb and back of the index finger
  • T4 level of the nipples
  • T10 umbilicus
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28
Q

Where are cell bodies of the body and face found?

A
  • Dorsal root ganglia for the body

- Trigeminal ganglia for the face

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29
Q

Describe the somatosensory pathway from the face

A
  • Enters the brain at the pons
  • Synapses in the trigeminal nucleus decussate
  • Secondary project to the thalamus (ventral-posteriomedial nucleus)
  • Tertiary sensory neurons project to the somatosensory cortex
30
Q

Describe the somatosensory pathway from the lower and upper limbs

A
  • Sensory information is carried at the cuneate fasciculus (upper limb - lateral) and gracille fasciculus (lower limb - medial)
  • Crosses over at the medulla to form the medial lemiscus tract
  • Connect to the thalamus, axons synapse with neurons in the ventral posteriolateral nucleas
  • Tertiary neurons to the primary somatosensory cortex
31
Q

How are dorsal horn neurons divided?

A

Those with axons that project to the brain (projection neurons) and those with axons that remain in the spinal cord (interneurons)

32
Q

What is lateral inhibition?

A
  • Lateral inhibition aids localisation of a stimulus by inhibiting neighbouring neurons becoming excited
  • This enhances the effect of the stimulus
33
Q

How is lateral inhibition mediated?

A

By inhibitory interneurons within the dorsal horn

34
Q

Where do first order neurons terminate in the dorsal column medial lemiscus tract?

A
  • Gracile tract have a synapse in the Gracile Nucleus

- Cuneate tract in cuneate nucleus

35
Q

Where do second order neurons decussate in the dorsal column medial lemiscus tract?

A
  • Caudal medulla

- Forms the contralateral medial lemniscus tract

36
Q

Where do the axons of second order neurons terminate in the dorsal column medial lemiscus tract?

A
  • Ventral posterior lateral nucleus of the thalamus

- Topographic representation of the body in the VPL (lower extremities are lateral)

37
Q

Where do the axons of third order neurons terminate in the dorsal column medial lemiscus tract?

A
  • 3rd order neurons from the VPL project to the somatosensory cortex
  • Size of somatotopic area is proportional to the density of sensory receptors in that body region
38
Q

Where do 1st order neurons terminate in the spinothalamic tract?

A
  • In the dorsal horn

- Terminate upon entering the spinal cord, and then immediately decussate to form the spinothalamic tract

39
Q

Where do 2nd order neurons terminate in the spinothalamic tract?

A
  • Terminate in the ventral posterior lateral nucleus of the thalamus
40
Q

What are the issues with sensory testing?

A

Psycholphysical assessment - it is subjective and affected by cooperation

41
Q

What is the importance of qualitative sensory testing?

A
  • Temperature and pain tests the integrity of the spinothalamic tract
  • Testing discriminative touch and 2-point discrimination tests the dorsal column
42
Q

List the affects of an anterior spinal cord lesion

A
  • Blocked anterior spinal artery causes ischemic damage to the anterior part of the spinal cord
  • Spinothalamic tract damage causes pain and temperature loss below the level of the lesion
  • There is retained light touch, vibration and 2-point discrimination
43
Q

Define pain

A

An unpleasant sensory and emotional experience associated with actual or potential tissue damage, or described in terms of such damage

44
Q

List the fibres involved in nociceptors

A
  • A delta fibres mediate sharp, intense or first pain (type 1: noxious mechanical and type 2: noxious heat)
  • C-fibres mediate dull aching or second pain (thermal, mechanical and chemical stimuli, reminding you to guard this site)
45
Q

How are nociceptors tested?

A
  • Pressure
  • Thermal stimuli
  • Sharp pin pricks
46
Q

What happens in the process of spinal cord nociceptive processing?

A
  • Glutamate is excitatory - major neurotransmitter for pain signalling
  • Released in response to acute or persistent noxious stimuli
  • Carried by a delta or C fibres to the dorsal part of the spinal cord
47
Q

How is pain, both the sensory and emotional components, transmitted?

A
  • Lateral spinothalamic tract (sensory component)

- Spinoreticular tract (emotional component)

48
Q

Where is activity seen in the brain following fMRI and painful stimulus?

A
  • SI, SII
  • Insula cortex
  • Anterior cingulate cortex
  • Prefrontal cortex
  • Amygdala
  • Cerebellum
  • Brainstem
49
Q

Describe the gate control theory of pain

A
  • Inhibition of primary afferent inputs before they are transmitted to the brain through ascending pathways
  • This explains why you want to rubbing a part of the body that has been hit before the feeling of pain (rubbing stimulates A beta neurons which inhibit the transmission of C fibres)
50
Q

List the descending control pathways of pain and the key areas of the brain involved

A
  • Strong emotions can inhibit pain
  • Electrical analgesia can reduce pain
  • Periaqueductal grey
  • Facilitation and inhibition of nociceptive processing in the dorsal horn
  • Monoamines have a role (serotonin and noradrenaline)
  • Opiods respond the same way, as well as placebo’s
51
Q

What are the types of chronic pain?

A
  • Nociceptive pain (related to the skin, muscles, bones or viscera) - arthritis, headache, fractures
  • Neuropathic pain (related to a lesion or disease in the somatosensory system) - sciatica, post surgical, trauma
  • Mixed - osteoartritis and low back pain
52
Q

What is peripheral sensitisation?

A
  • Damaged tissue releases inflammatory soup (chemicals such as neurotransmitters, peptides, lipids, proteases and cytokines)
  • These produce inflammation, and also modulate excitability of nociceptors to make them more receptive to pain
  • Decreases the threshold to stimuli at the site of injury
53
Q

What is central sensitisation?

A
  • Decreases the threshold to peripheral stimuli at an adjacent site to the injury
  • Expands the receptive field causing spontaneous pain
54
Q

What is allodynia?

A

Pain due to a stimulus that does not normally provoke pain

55
Q

What is hyperalagesia?

A

Increased pain from a stimulus that normally provokes pain (primary at the site and secondary when around the site)

56
Q

How is diagnosis and assessment of neuropathic pain performed?

A
  • Must have an injury or disease to the somatosensory system
  • Symptoms must be present in an area consistent with the sensory involvement
  • Identify either sensory loss or sensory pain
  • Neuropathic pain questionairres are used to assist this
57
Q

What drugs are effective in neuropathic pain?

A
  • Serotonin selective re-uptake inhibitors are not effective
  • Serotonin noradrenaline re-uptake inhibitor and tricyclic antidepressants are more useful
  • Noradrenaline has a protective effect, while serotonin is a facilitator of chronic pain
58
Q

How does conditioned pain modulation occur?

A
  • Pain inhibits pain (eg. pressure pain and heat)

- This is because the threshold increases or the pain decreases

59
Q

What is the function of the dorsal column system?

A
  • Conveys innocuous mechanical stimuli (fine discriminative touch and vibration)
  • Uses A beta fibres
60
Q

List the two spinothalamic pathways

A
  • Pain and temperature ascend within the lateral spinothalamic tract (a delta)
  • Crude touch ascends within the anterior spinothalamic tract (A beta)
61
Q

Define the term adaptation

A
  • The decline of the electric responses of a receptor neuron over time in spite of the continued presence of a stimulus of constant strength.
  • This change is apparent as a gradual decrease in the frequency of action potentials generated.
62
Q

What is the representation of the body like in the ventral posterior lateral nucleus of the thalamus?

A
  • Topographic representation

- Lower extremities are lateral

63
Q

Compare the localisation of pain and temperature to that of touch and vibration

A
  • Size of somatotopic areas is proportional to the density of receptors in that body region in regard to touch and vibration
  • Pain and temperature location is not as precise
64
Q

What type of receptors detect touch and proprioception?

A

Mechanoreceptors

65
Q

Compare the receptive fields of nociception and touch

A
  • Touch is much more specific

- Nociception much larger fields

66
Q

Where do the third order neurones go in the spinothalamic tract?

A
  • Relays through the ventral posteriolateral nucleus to the primary somatosensory cortex
67
Q

How are the spinothtamic tract and dorsal column different?

A
  • In spinothalamic, information from the lowest parts are lateral and the highest parts are medial
  • In the dorsal column the information from lower is medial and from higher is lateral
68
Q

Describe the pathway of nociceptive information from the face

A
  • Comes via the trigeminal nerve
  • Into trigeminal ganglion at the level of the pons
  • Goes down alongside trigeminal nucleus, synapses in the trigeminal nucleus at the level of the medulla
  • This second neuron then joins the medial end of the spinothalamic tract, to synapse with the ventral postereomedial nucleus and finally primary somatosensory cortex
69
Q

Which sensory neurons decussate?

A

Second order neurons

70
Q

Why is overlapping of sensory neurones receptive field important?

A
  • As this allows the precise location of a stimulus to be detected
  • Depending on the exact location of the stimulus, different neurons will be stimulated at different frequencies
71
Q

How does sensory convergence affect receptive field size?

A

If many primary neurons converge to a single sensory neuron, the receptive field will be larger