Somatosensory system Flashcards

1
Q

What are the functions of the somatosensory pathways? What does it generally consider?

A

Ability to interpret bodily sensation
Mechanical, thermal, proprioceptive, nociceptive (anything negative)
Consists of skin, tissue, joints, nerves, spinal cord and brain

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2
Q

What are the different somatosensory modilities?

A

Mechanical, Thermal, Proprioceptive, Nociceptive

Modalities mean each of these different nerves

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3
Q

What do the terminals of sensory nerves look like?

A

Modifed nerve endings - free nerve endings-thermoreceptors and nociceptors
Enclosed nerve ending-mechanorecptors

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4
Q

What are the 3 main classes of sensory neurons

A

Aalpha-motor
Abeta-smaller than Aa but faster than res, mechanoreceptors of skin (large and fast), myelinated increase speed (m/sec)
Reaches CNS before pain
Agamma-nociceptors and mechanical stimuli (smaller than Ab)
C-Unmyelinated, smaller- slower-pain temperature, itch

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5
Q

Define receptor. What types of thermoreceptors are they?

A

Receptors are transducers that convert energy from the environement to Action potential
Themroreceptors-Agamma, C fibres-sensitive via membrane. Very sensitive, but not evenly distributed
Free nerve endings
Temp ability depends of what receptors (TRP ion channels)-4heat activated ion channels (TRPV1-4), 2 cold activated-TRPM8/A1 (activated by wasabi)
MEchanoreceptors

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6
Q

Define the 5 main mechanoreceptors

A

Meissners corpuscules (fine discriminative, low frequency vibration)
Merkel cells-light souch, superficial oressure
Pacinian corpuscule-deep pressure, high frequency vibration
Ruffini endings-continous pressure and stretch
ALL are Abeta type fibres

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7
Q

Define stimulus threshold

A

Point of intensity where a person can detect the stimulus 50% of the time (like microfilaments-which thickness)

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8
Q

Define stimulus intensity

A

Define by how much a neuron fires above its threshold-with longer/stronger timulus, more AP leading to increased sensrory

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9
Q

What are tonic receptors?

A

Detect continous stimulus strength- but adapt very slowly/dont adapt
fire all the time of the stimulus-keeps brain informed
MERKEL cells are a type of that

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10
Q

What is adaptation?

A

Detection of continous stimulus strength-your body wont keep telling you about it if nothing changes (like a hand on a table for long)-only stimlus at start and end

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11
Q

What are Phasic receptors?

A

They detect change in stimulus strengtgh-only fire when there is a change-adapt fast
Pacinian recepot-fire start and end of pressure, not in between

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12
Q

What is a receptive field>

A

Region of the skin which activates only 1 sensory neuron
Different sizes in places
Upper arm have large ones-so cant differciate too much
Fingers have timy ones, which allows very precise
Back is super large-reduced precision

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13
Q

What is two point discrimination?

A

Minimun distance at which 2 points are considered diferent
Usually dependent on the size of the receptive field
Vary wildly between body-hand is 4/5mm, but back/calf is over 45mm

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14
Q

What are somatosensory dermatomes?

A

area of skin innvervated by a sigle spinal nerve
Each nerve has a ventral and dorsal root
Provide a mapping system to see where sensory is going
C5-clavicule, C6 (6 shooter)-thumb. T4 is nipples, T10 is belly body

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15
Q

Where are the cell bodies for neurons in body and face?

A

body dorsal root ganglia in body, and trigeminal ganglia for face
Legs go up gracile fasciculutus, and arms go up the cuneate fasciculutus -cross over in the medulla to thalamus
(gracile more medial than cuneate)
Trigeminal go directly via pons to trigeminal nucleus, then to thalamus

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16
Q

What are the two neuron types in the dorsal horn>

A

Those that prokect to brain (projection neurons)-
And interneurons that remain in spinal cord
Thermo and noci (Adelta/C fibre-are more superficial)
Ab are deeper in the dorsal horn

17
Q

What is lateral inhbition?

A

Explain how receptive fields can overlap with other-difficult to distinguish
In the dorsal horn, inhbitory interneuron stop from adjacent neurons from being activated too, increasing perception

18
Q

Describe the touch and proprioception tract

A

Ab fibres via dorsal horn to dorsal columjn pathays
Via fasciculutus gracilis(under T6)/Cuneatus (above T6)
On the SAME SIDE (ipsilateral) and cross over (dessecate) in medulla
Do fine discriminative touch and vibration
1st order neuron to medulla each synapse within cuneate/gracilis nuclei in medulla
2nd order go to caudal medulla -form contralateal lemniscus tract
2nd order neurons teperminate in ventral posteror lateral nuctleus of thalamis (VPL)
3rd order neurons terminate in somatosensory cortex-size of area in brain depends on densirty of fibres from that area (hand massive)

19
Q

Describe the ascending pathway for pain, temperature and crude touch

A

Carried in SPINOTHALAMIC pathway (pain/temp-lateral, Crude touch in the anterior)
CROSS OVER at the same level as they enter (immediate), then go up to thalamus/somatosensory cortex
1st order terminate in spinal cord/dorsal horn
2nd orderneuron cross over and to thalamus to ventral posterio lateral nucleus (VPL)

20
Q

What is the clincal relevance of 2 point discrimination test

A

Called psychophysical assessment-depends on patients a lot
Tests the integrity of acending-can test sensation. pain, discrimation (dorsal column)
In anterior spinal artery damge-lose spinothalamuc tract below lesion-BUT dorsal part is intact (light touch, vibration, 2point discrimation)

21
Q

Define pain rohgly

A

Unpleasent sensory and emotional experience associated with actual or potential tissue damage

22
Q

Describe Nociceptors types and roles

A

Adelta fibres-type 1 noxious mechanical, noxious heat-fast sharp pain
C fibres mediate the dull/aching pain

23
Q

What is the neurotransmitter used in pain processing?

A

Glutamate released as an answer to the stimuli, to the dorsal root then can go to several levels-physical and emotion/learning

24
Q

How is pain carried to the brain

A

Sensroy is carried via lateral spinothalamic tract, but spinoreticular tract carries the emotion component
In the brain, involves incredible amounts of part (frontal, amygdala, cerebellumn brainstem, etc

25
Q

Explain how nociceptor input can be gated by CNS

A

Gate control theory-Inhbition of primary afferent inputs before they are transmitted to brain
Like rubbing elbow after hitting it-activating Ab fibers to activate inhbitory neurons, stopping C Fibre info from passing to brain
Also descending control pathways-strong emotions can inhbit pain-involved periaqueductal grey-facilitation and inhbition of nociceptive precessing. Use serotonin/noradrenaline (opiods similar)
Placebo seems to do that

26
Q

What are the main mechanisms of chronic pain?

A

Pain that last over 3 month-
Can be nociceptive pain-skin, msucle, ligaments, etc (arthirits) or neuropathic pain (sciatica, trauma, diabete)c
Also mixed pain-lower back pain, osteoarthiritis

27
Q

What is peripheral sensitisation?

A

As an area is damaged, create a inflmatory soup-create inflamation, but also modulate nociceptors or the area
make it more sensitive (reduce threshold but peripherally and centrally (via plasticity of projection neuron of dorsal horn)

28
Q

Define Allodynia and hyperalgesia

A

Allodynia-Pain due to stimulus that doesnt normally provoke pain
Hyperalgesia-increased pain from normally painful stimuli (primary-at the area of damge, secondary-around) -pretty much reduce stimulus threshold needed

29
Q

How do you diagnose neuropathic pain?

A

Very filtered-has to have neurological damage. Symptoms have to match. Have to have sensory lose or gain
Usually start with questionnaires, but not diagnostic

30
Q

What are the 3 main neuropathic pain cluster types

A

Sensory loss, Thermal hyperalgesia and mechanical hyperalgesia