Sensory Systems Flashcards

1
Q

Physiological receptors are

A

sensory receptors

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2
Q

Pharmacological receptors are

A

protein receptors

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3
Q

All sensory receptors transduce their adequate stimulus into

A

a depolarisation signal which produces the receptor (generator) potential

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4
Q

What type of potential is the receptor potential?

A

Graded local detrimental potential

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5
Q

The size of the receptor potential is related to

A

the intensity of the stimulus

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6
Q

The receptor potential triggers

A

the firing of action potentials

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7
Q

Action potentials are always the same size, so intensity of the stimulus is determined by

A

the frequency of action potentials rather than their size

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8
Q

The receptive field encodes

A

the location of the stimulus, giving information on the modality, intensity and location of the stimulus

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9
Q

Thermoreceptive and nociceptive information travels via what fibres?

A

A-delta and C fibres

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10
Q

Where do A-delta and C fibres synapse?

A

In the dorsal horn

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11
Q

A-delta and C fibres come through the dorsal horn and almost immediately synapse onto

A

the second order fibre

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12
Q

The second order fibres of A-delta and C fibres cross over

A

in the midline of the spinal cord

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13
Q

Once the second order fibres of A-delta and C fibres have crossed over, they

A

project up through the contralateral spinothalamic (anterolateral) tract to the reticular formation, thalamus and cortex

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14
Q

Damage to the spinothalamic (anterolateral) quadrant causes

A

loss of nociceptive and temperature sensation below the lesion on the contralateral side

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15
Q

Mechanoreceptive information travels via what fibres?

A

A-alpha and A-beta fibres

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16
Q

A-alpha and A-beta fibres project

A

straight up through the ipsilateral dorsal columns of the spinal cord

17
Q

A-alpha and A-beta fibres synapse

A

on the same side, in the cuneate and gracile nuclei

18
Q

The second order fibres of A-alpha and A-beta fibres cross over

A

in the midline of the spinal cord and synapse in the brain stem

19
Q

Once the second order fibres of A-alpha and A-beta fibres have synapsed in the brain stem, the information goes to

A

the reticular formation, thalamus and cortex

20
Q

Signal transduction in nociceptors is activated by

A

Low pH
Heat
Local chemical mediators

21
Q

When are local chemical mediators released?

A

When the skin is crushed, leading to depolarisation, action potential firing and excitation of the nociceptors

22
Q

Bradykinin, histamine and prostaglandins are examples of

A

local chemical mediators

23
Q

How is low pH detected and what does this cause?

A

an acid sensing ion channel (ASIC) which opens its integral ion channel to cause depolarisation, action potential firing and excitation

24
Q

Noxious heat causes what ion channel to open?

A

VR1 ion channel

25
Q

Why might pain originating from the viscera cause referred pain to a somatic structure from the same dermatome?

A

Visceral pain is generally poorly localised

Convergence of sensory fibres - fewer neurones reduces the acuity

26
Q

According to the gate control theory, pain signals

A

are not free to reach the brain as soon as they are generated at the injured tissue/site

27
Q

Pain signals need to encounter

A

neurological gates at the spinal cord level which determine whether the pain signals should reach the brain or not

28
Q

Pain is perceived when

A

neurological gates give way to the pain signals

29
Q

Pain is less intense or not perceived when

A

the neurological gate closes

30
Q

Peri-aqueductal grey matter cell bodies transmit to the

A

nucleus raphe magnus

31
Q

Fibres travel from the nucleus raphe magus down what?

A

The spinal cord and descending tracts

32
Q

Function of peri-aqueductal grey matter cell bodies that transmit to the NRM

A

Activate inhibitory interneurons that release opioid peptides and stop the transmitter release, closing the neurological gates

33
Q

Function of prostaglandins

A

release G proteins when stimulated which sensitise the nociceptors to bradykinin

34
Q

Why do NSAIDs work well against pain associated with inflammation?

A

They are anti-pyretic and anti-inflammatory

They inhibit cyclo-oxygenase which converts arachidonic acid to prostaglandins (prostaglandins sensitise nociceptors)

35
Q

Local anaesthetics block

A

the voltage gated sodium channels from transmitting the action potential and therefore block axonal transmission

36
Q

How does transcutaneous electric nerve stimulation (TENS) work?

A

Electrically stimulates the nerve fibres to close the gate

37
Q

How do opiates e.g. morphine work?

A

Reduce sensitivity of nociceptors
Block transmitter release in the dorsal horn
Activate descending inhibitory pathways

38
Q

What route of opiate administration is most effective and why?

A

Epidural
Allows them to be delivered around the spinal cord where they have best access to the synapses at the top levels of the spinal cord and can block transmission