Sensory systems Flashcards

1
Q

What are the different types of sensory receptor?

A

Mechanoreceptors - touch

Chemoreceptors - chemical shit

Thermoreceptors - heat

Nociceptors - pain (dont call them pain receptors though)

Proprioceptors - joint movement and all that stuff

Probably some others but i cba

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2
Q

What are the different types of sensory receptors that are found?

identify them on the photo below

A

A - Meissner’s corpuscle - Light touch

B - Merkle’s corpuscle - Touch

C - Free nerve ending - Pain

D - Pacinian corpuscle - Deep pressure

E - Ruffini corpuscle - Heat

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3
Q

How do different types of sensory receptors differ in terms of their complexity of structure?

A

Some are simple (free nerve endings) such as nociceptors, cold receptors

Some have much more complex structures that you need to know - eg Pacinian corpuscles (Deep pressure) & Meissner’s corpuscles (light touch)

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4
Q

What is meant by the term ‘transduction’ when talking about sensory receptors

A

Adequate stimulus will cause sensory receptors to transduce it into a depolarisation

This depolarization is called the Receptor (or Generator) potential

The size of the receptor potential encodes the intensity of the stimulus

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5
Q

How do receptor potentials travel through the body?

A

Adequate stimulus = receptor potential produced

The receptor potential then evokes the firing of action potentials which travel in the body

The frequency of these APs encodes the intensity of the stimulus

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6
Q

What is the receptive field?

A

Receptive field is a portion of sensory space that can elicit neuronal response when stimulated

Ie its the area corresponding to a specific nerve - this allows us to pinpoint the location that a stimulus acts on us

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7
Q

Shown below are membrane potential readings from different parts of a neuron when stimulated in 2 different ways

What is the difference between the 2 stimuli and how?

A

The top stimulus - Shorter & weaker:

  • Smaller receptor potential indicates lower stimulus intensity
  • Lower frequency of action potentials = low stimulus intensity
  • Lower duration of AP series = shorter duration

Bottom stimulus - Longer & more intense:

  • Receptor potential longer with more depolarisation
  • Action potentials have higher frequency and the series of APs lasts longer
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8
Q

Some areas of the skin have lots of sensory receptors with small receptive fields

Some have few receptors with large visual fields

How is this relevant to acuity?

A

Lots of receptors with small areas they cover = high acuity. You can distinguish between 2 stimuli at a pretty short distance from each other

In order to distinguish 2 points from each other - each point must stimulate a different receptive field

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9
Q

What are the 3 types of primary afferent fibres that transmit cutaneous signals?

A

  • 2nd Largest myelinated fibres
  • 30-70 m/s
  • Touch, pressure, vibration

  • Smallest myelinated fibres
  • 5-30 m/s
  • Cold, “fast” pain, pressure

C

  • Unmyelinated
  • 0.5-2 m/s
  • Warmth, “slow” pain
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10
Q

What types of primary afferent fibres mediate proprioceptive sensation?

A

eg muscle spindles, golgi tendon organs etc

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11
Q

Where do primary afferent fibres enter the CNS?

A

Either enter through dorsal root ganglia or cranial nerve nuclei

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12
Q

What types of fibres correspond to mechanoreceptive information and how do these travel through the CNS?

A

Aα & Aβ - mechanoreceptive fibres

Project straight up through ipsilateral dorsal columns

Synapse in cuneate & gracile nuclei

2nd order fibres cross over midline (decussate) in the brain stem & project to reticular formation, thalamus and cortex

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13
Q

How do nociceptive and thermoreceptive fibres travel through the CNS?

A

Aδ & C

synapse in the dorsal horn

the 2nd order fibres cross over the midline in the spinal cord

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

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14
Q

In the diagram below, identify the sensory modalities and fibre types that correspond to that diagram

A

Left:

  • Mechanoreceptors - Aα & Aβ

Right:

  • Nociceptors & thermoreceptors - Aδ & C
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15
Q

What would be the effect on sensation of damage to the:

A) Dorsal columns

B) Anterolateral quadrant

A

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

B) causes loss of nociceptive & temperature sensation below lesion on contralateral side

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16
Q

What is meant by ‘adaptation’

A

When a stimulus is applied - sensory receptors will transduce it and action potentials are produced

If a stimulus is applied over a long period of time - certain receptors will adapt to the stimulus and will stop firing action potentials until the stimulus is removed or changes

This is why you cant feel your clothes touching you unless you move - as the mechanoreceptors adapt

17
Q

What is convergence?

A

Basically multiple primary afferent neurones converge on the same secondary neuron

Saves neurones but reduces acuity

May also underlie referred pain

18
Q

What is lateral inhibition?

A

Imagine pressing a pin against your skin…

Small area of contact (sharp) however the skin (and thus mechanoreceptors) around the point will be stretched

This would lead to a broad area being stimulated and thus ‘felt’

Lateral inhibition means synaptic inhibition of surrounding sensory inputs so you only feel the actual point

19
Q

What is the difference between rapidly adapting and slowly adapting?

A

Rapid:

  • Will quickly stop firing action potentials after the stimulus begins
  • There is a small burst of APs when the stimulus is removed
  • eg - imagine putting on a hat

Slow:

  • Initial quick burst but will continue firing for some time
  • eg - in the stretch reflex - there are some Slow adapting ones that monitor the muscle length
20
Q

“Not all information reaches the brain”

What is meant by this?

A

Our brain couldn’t handle all the sensory information coming from all round the body

There are tons of descending inhibition that stops the (background) information from reaching the brain

21
Q

What is the difference between perception and sensation?

A

Sensation refers to everything that is sensed by the body (funnily enough)

Perception is the portion of what we sense that we are aware of - ie what we perceive

22
Q

What accounts for the differences between fast and slow pain?

A

‘Fast pain’ is transmitted by Aδ fibres

‘Slow pain’ is transmitted by C fibres

Difference in speed of transmission accounts for initial sharp pain when stubbing toe - and the delayed hit of pain when you start swearing

23
Q

Nociceptors have endings that have an abundance of receptors and channels in the membrane

What important channels are present and what stimulates them?

A

ASIC - Acid Sensing Iron Channels:

  • low pH causes depolarisation

VR1

  • Noxious heat stimuli causes depolarisation

B2 Bradykinin receptor (and other similar proteins)

  • Bradykinin released when tissue is crushed
  • Binding causes depolarisation
24
Q

What spicy thing can happen here involving nociceptive and mechanoreceptive transmissions?

A

This synapse acts as a gate for Nociceptive (pain) information

Transmission of Mechanoreceptive information up the A(beta) will inhibit the Nociceptor fibre at its synapse in the dorsal horn (stopping the pain transmission)

This is through a small branch that goes off the Mechano fibre at the site of the Nocic. synapse

That’s why rubbing/holding an injured area can make it feel better

25
Q

What is meant (for all this pain stuff) by descending control?

A

As well as Mechanorecptive inhibition - Descending controls come from the periaqueductal grey matter (PAG) which sends impulses to the Nucleus Raphe Magnus (NRM)

Neurones from the NRM travel down the spinal cord to near the Nociceptor synapse in the dorsal horn and activate the inhibitory neuron - thus stopping the pain transmission

26
Q

Shown below is part of the nociceptor nerve ending - specifically the Bradykinin receptor

Describe the effect of prostaglandin

A

Prostaglandin basically makes the Bradykinin receptor more sensitive basically - so Bradykinin’s effect becomes less strong

27
Q

How do NSAIDs work?

A

NSAIDs are analgesic (and antipiretic & anti-inflammatory)

They inhibit cyclo-oxygenase which converts arachidonic acid to prostaglandins

Inhibit production of Prostaglandins = stop them sensitising Bradykinin receptors = less depolarisation

28
Q

How do local anaesthetics typically work?

A

Block Na+ action potential and therefore all axonal transmission

29
Q

How does Transcutaneous electric nerve stimulation (TENS) work?

A

Electric pads are placed on affected area and an electric current is passed through that stimulates A(alpha) and A(beta) fibres

As we know - mechanoreceptor stimulation will inhibit nociceptive transmission so in theory the pads will reduce the pain sensation

30
Q

In what 3 ways do opiates reduce pain sensation?

A

Reduce sensitivity of nociceptors

Block transmitter release at the dorsal horn synapse

Activate descending inhibitory pathways

31
Q

How do Opiates reduce the sensitivity of nociceptors?

A

Nociceptors have an opioid/opiate receptor in the membrane of their nerve endings

When activated - this receptor will cause the hyperpolarisation of the cell through a potassium channel

This reduces the size of the receptor potential & thus action potential frequency etc etc

32
Q

How do opiates block transmitter release in the dorsal horn?

A

Opiates activate the same opioid receptors at the nociceptor gate - thus closing it

Hence its use in Epidural anaesthetic

33
Q

How do opiates activate the descending inhibitory pathways?

A

In the PAG - opiates cause depolarisation (instead of hyperpolarisation)

Neurones then activate the next in the NRM and so on