Sensory system - including physiology of pain Flashcards

1
Q

Each sensory information is associated with a specific receptor type, name 5 receptors

A

Mechanoreceptor - mechanical stimuli

Chemoreceptor - chemical stimuli

Thermoreceptor - sensory temp

Nociceceptor - pain

Proprioceptors - muscle spindles

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2
Q

Define receptve field

A

Response to a stimulus over a specific area

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3
Q

What is the different structures of sensory receptors

A
Pacinian corpuscle 
(deep pressure)
Messiners corpuscle (light touch)
Free nerve ending (pain)
Ruffin corpuscle (warmth)
Merkels corpuscles (touch)
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4
Q

How do sensory (physiological) receptors work in signal tranductions

A

transduce their adequate stimulus into depolarisation, creating a receptor (generator) potential

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5
Q

What encodes the intensity of stimulus

A

The size of the receptor potential

affecting the frequency of action potentials

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6
Q

What does the receptor potential evoke

A

Firing of action potential for long distance transmission

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7
Q

What is the function of the receptive field

A

Encode location of stimulus

giving info on intensity and modality

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8
Q

What determines acuity

A

Density of innervation, and size of receptive fields,

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9
Q

Cutaneous sensation is mediated by what 3 types of primary afferent fibres

A

Aβ = large myelinated (30-70m/s)

Aδ = small myelinated (5-30m/s)

C = unmyelinated fibres (0.5-2m/s)

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10
Q

What are A alpha fibres responsible for what cutaneous sensation

A

Transmission of touch, pressure, vibration sees

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11
Q

What are A delta fibres responsible for what cutaneous sensation

A

Transmission of cold, “fast” pain, pressure senses

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12
Q

What are C fibres responsible for what cutaneous sensation

A

Transmission of warmth, “slow” pain senses

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13
Q

What two primary afferent fibres are responsible for proprioception

A

A alpha

A beta

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14
Q

Define acuity

A

Ability to locate a stimulus & to differentiate it from one nearby

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15
Q

Where do all primary afferent fibres enter the spinal cord

A

Via the dorsal root ganglia

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16
Q

What is the transmission pathway of mechanoreceptive fibres (Aα & Aβ) to first synapse

A

Project straight up through ipsilateral dorsal column pathway and synapse in cuneate and gracile nuclei of the medulla

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17
Q

Where do second order mechanoreceptive fibres decussate

A

Brain stem

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18
Q

Where does second order mechanoreceptive fibres project and synapse

A

Via the contralateral medial lemniscus

synapsing in the Reticular formation, thalamus

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19
Q

Where does first order thermoreceptive and nociceptive fibres (Aδ & C) synapse

A

In the dorsal horn

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20
Q

Where does second order thermoreceptive and nociceptive fibres (Aδ & C) cross over

A

The midline in the spinal cord

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21
Q

What tract do the second order thermoreceptive and nociceptive fibres project up

A

contralateral spinothalamic (anterolateral) tract

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22
Q

Where do the second order thermoreceptive and nociceptive fibres synapse

A

reticular formation, thalamus

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23
Q

What is the pathway of third order neurone of the mechanoreceptive, thermoreceptive and nociceptive fibres and where do they synapse

A

Ascend from the ventral posterolateral nucleus of the thalamus, travel through the internal capsule and terminate at the sensory cortex

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24
Q

What is the clinical consequence of damage to dorsal columns

A

causes loss of touch, vibration, proprioception below lesion on ipsilateral side

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25
What is the clinical consequences of damed to anterolateral quadrant
causes loss of nociceptive & temperature sensation below lesion on contralateral side
26
Where does ultimate termination of sensory information occur
somatosensory cortex (S1) of the postcentral gyrus
27
How does the somatosensory cortex produce a sensory homunculus
Sensory transmission endings are grouped according to the location of the receptors extent of sensory representation is related to the density of receptors in each location
28
What allows processing of sensory pathways
Adaptation Convergence Lateral inhibition Not all info reaches the brain - filtration Perception
29
When does adaptation of receptors occurs
When receptors are continually stimulated by a maintained stimuli
30
What does adaption result in
Receptors become less sensitive, or switch off
31
What is the difference between rapid and slow adapting cutaneous receptors?
Rapidly adapting receptors are best at detecting rapidly changing signals, while slowly adapting receptors are capable of detecting a long, continuous signal
32
What stimuli does not trigger adaptation
Painful stimuli
33
What is the features of convergence
Saves on neurones Reduces acuity and can underlie referred pain
34
What occurs in lateral inhibition
activation of one sensory input causes synaptic inhibition of its neighbours
35
What is the benefit of lateral inhibition
Gives better definition of boundaries - enhances perception Cleans up sensory information
36
How does perception affect the processing in sensory pathway
Importance of inputs varies according to your state of mind
37
What activates signal transduction in nociceptors
Low pH Heat Local chemical mediators
38
What is the usually cause of referred pain
Convergence of visceral pain fibres and skin pain fibres
39
What is the structure of nociceptors
Free nerve ending
40
What nociceptors directly respond to damaged stimuli
ASIS | VR1
41
What direct nociceptor responds to low pH
ASIS
42
What direct nociceptor responds to heat
Vr1 receptors
43
What are the indirect hormones released that stimulate noceiceptor
Bradykinin, Histamine, Prostaglandins all released with tissue damage
44
What does stimulation of nociceptors result in
Transduction as depolarisation of cells occurs due to the opening of sodium and potassium channels and an AP is fired
45
What nerve fibres does the nociceptive AP travel in
``` C fibres (slow pain) A delta fibres (fast pain) ```
46
Where does C/ A delta fibres synapse
In the dorsal route of the spinal cord
47
How is the gate closed in controlling pain in the spinal cord
By an Inhibitory interneurone release opioid peptidase and inhibits the release from A delta/C fibres
48
What two controls allow the closing of the gate
Segmental | Descending
49
How does segmental control close the gate
An active A beta activates inhibitory interneurone
50
How does deadening control close the gate
Cell bodies from Periaqueductal Grey Matter (PAG) and Nucleus Raphe Magnus (NRM) - sends axons down the spinal cord and activates inhibitory interneurons
51
How does prostaglandins cause analgesia
Sensitises nociceptors to bradkyinin Activates voltage gates sodium channel
52
How does bradykinin cause analgesia
Activates VR1 receptor
53
How does NSAIDS work in treating analgesia
because they inhibit cyclo-oxygenase which converts arachidonic acid to prostaglandins
54
What is the affect of prostaglandin have on the body
Inflammation Pain Fever
55
How does local aesthetics treat analgesia
block Na+ action potential and therefore all axonal transmission
56
What is transcutaneous electrical nerve stimulation
Low-voltage electrical current for pain relief The stimulating pulses across the skin help prevent pain signals from reaching the brain
57
How does opiates work in treating analgesia
reduce sensitivity of nociceptors block transmitter release in dorsal horn (hence epidural administration) activate descending inhibitory pathways
58
What does the Nucleus Raphe Magnus release when stimulated
5-HT (serotonin) released from the raphe nuclei descends to the dorsal horn of the spinal cord
59
What stimulates the nucleus raphe magnus
Stimulation of the periaqueductal gray matter of the midbrain activates enkephalin-releasing neurons that project to the raphe nuclei in the brainstem
60
Where is the the periaqueductal gray matter
The periaqueductal gray is the gray matter located around the cerebral aqueduct within the tegmentum of the midbrain