Sensory Processing Flashcards

1
Q

How is the selectivity of afferent fibres partly conferred?

A

protein macromolecules

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2
Q

What are C-MH fibres?

A

C-fibres responsive to heat and mechanical stimuli

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3
Q

What is the temperature at which sensation becomes noxious to humans and animals?

A

42-45º

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4
Q

Where is elkin1 present?

A

Aβ , Aδ and some C afferent fibres

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5
Q

What is elkin1 important for?

A

non-noxious stimuli response

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6
Q

What is Elkin1 a modulator of?

A

non-painful cutaneous responses

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7
Q

What are TRP receptors for?

A

sensing noxious thermal stimuli

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8
Q

What is mechanical noxious stimulus mainly driven by?

A

other molecules not present on Aβ afferent fibres

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9
Q

Why do different afferents show selectivity to different stimuli?

A

because of protein macromolecules present on the associated receptors

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10
Q

What is adequate stimulus property?

A

the kind of stimulus to which a receptor is especially sensitive

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11
Q

What are label lines?

A

the primary afferents and their associated receptors important for encoding the nature of the stimulus.

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12
Q

How do warm excited neurons respond to warmth?

A

by increasing their activity

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13
Q

What is TRPV1 important for?

A

response in the painful range

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14
Q

What is TRPM8 important for?

A

response in the non-painful range

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15
Q

What happens to warm inhibited sensory neurons when they are cooled and warmed?

A
  • cooled = increase in activity of primary afferent
  • warmed = decrease in activity of afferent i.e. no AP discharged
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16
Q

What does PMBC do?

A

block TRPM8 channels and affect the ability of animals to detect warmth

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17
Q

What is disinhibition?

A

the reduction or removal of inhibitory control within neural circuits, leading to an increase in the activity of certain neurons or pathways

18
Q

What is disinhibition important for?

A

motor control, sensory processing, and emotional regulation

19
Q

What properties of a signal can an AP encode and what concept is associated with each?

A
  • quality - label line
  • intensity - frequency and population code
  • duration - slowly adapting receptor
  • location - receptive field
20
Q

What is frequency code?

A

the number of APs; relates to the strength of the stimulus

21
Q

What is population code?

A

the number of receptors activated; proportional to the force of contact

22
Q

What is the duration of an AP signalled by?

A

the speed of adapting

23
Q

What are rapidly adapting receptors important for?

A

detecting changes in stimuli, such as the onset or removal of pressure e.g. pressure to the skin

24
Q

What is the receptive field?

A

the area monitored by a receptor

25
Q

Where is the receptor and afferent most strongly excited?

A

at the point of contact i.e. point of maximum force

26
Q

How can a signal be further modulated?

A

inhibition in the CNS

27
Q

What do first order neurons do?

A

enter into the spinal cord and provide input to second order neurons

28
Q

What do second order neurons do?

A

contact other neurons and also inhibitory neurons via a side branch

29
Q

What do inhibitory neurons do?

A

contact second order neurons in adjacent areas

30
Q

What is stimulus location encoded and sharpened by respectively?

A
  • encoded by receptive field
  • sharpened by inhibition
31
Q

What is the first sensory relay of the CNS?

A

spinal cord

32
Q

What does a cross section of the spinal cord show?

A
  • grey matter rich in neurons
  • white matter rich in axons
  • dorsal horn in grey matter
  • dorsal column in top of white matter
  • ventrolateral column in bottom of white matter
33
Q

Where do pain pathways cross the midline?

A

in the spinal cord

34
Q

Where do fine touch pathways cross the midline?

A

in the medulla

35
Q

Where do sensory pathways synapse?

A

in the thalamus

36
Q

What is the touch (dorsal column) pathway responsible for?

A

transmitting touch, pressure, and proprioception

37
Q

What are the 5 steps of the touch (dorsal column) pathway?

A
  1. sensory receptors in the skin detect touch, pressure, or body position changes and generate nerve signals
  2. nerve signals travel through afferent fibres and enter the spinal cord through the dorsal column on the same side of the body
  3. the signals continue upward and reach the medulla, where they synapse with neurons in the dorsal column nuclei (gracile and cuneate nuclei)
  4. neurons in the medulla send their axons across to the opposite side of the brain, forming the medial lemniscus pathway
  5. the signals travel to the thalamus, which acts as a relay station, and then project to the primary somatosensory cortex, where the touch information is processed and perceived
38
Q

What is the pain (spinothalamic) pathway responsible for?

A

transmitting pain, temperature, and crude touch sensations

39
Q

What are the 5 steps of the pain (spinothalamic) pathway?

A
  1. nociceptors in the skin or tissues detect painful stimuli and generate nerve signals
  2. these nerve signals travel through Aδ /C afferent fibres and enter the spinal cord, where they immediately synapse with neurons in the dorsal horn
  3. neurons in the dorsal horn send their axons across to the opposite side of the spinal cord, where they join the spinothalamic tract
  4. the signals ascend through the spinothalamic tract, passing through the brainstem and reaching the thalamus
  5. the thalamus, acting as a relay station, forwards the signals to the primary somatosensory cortex, where the sensation is processed and perceived
40
Q

What does lesion in the dorsal column result in?

A

deficit in sensations of fine touch

41
Q

What does damage to the anterolateral (spinothalamic) tract result in?

A

loss of pain