General Sensation Flashcards

1
Q

What are sensory receptors?

A
  • Each type of sensory information is associated with a specific sensory receptor (mechan/chemo/thermo/nociceptors
  • Can either be free nerve endings (nociceptor) or complex structures (Pacininan corpuscle)
  • These receptors respond to stimulus over a specific area = RECEPTIVE FIELD
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2
Q

What are the different types of sensory receptors found in the skin?

A

Tactile: Light touch: Meissner’s Corpuscle

Tactile: Touch: Merkle’s Corpuscles

Pain: Free nerve ending

Deep pressure: Pacinian corpuscle

Warmth: Ruffini Corpuscle

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3
Q

What’s the process of Sensory transduction?

A
  1. Sensory receptor s transduce (physical energy into a nervous signal) their adequate stimulus into a depolarisation, the receptor (generator) potential
  2. The size of the receptor potential encodes the intensity of the stimulus - greater stimulus great chance of breaching threshold
  3. Receptor potential then evokes firing of action potentials for long distance transmission
  4. The frequency of action potentials encodes the intensity of stimulus with the receptive field encoding the location of stimulus
  5. Ends in neurotransmitter release
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4
Q

What determines Acuity (ability to discriminate between 2 points)?

A

The density of innervation and size of receptive field

  • Some parts of the body have neurons with small receptive fields - able to discriminate between 2 points
  • Some parts of the body have neurons with large receptive fields -unable to distinguish between 2 points of contact in that area
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5
Q

What are Primary afferent fibres?

A

Nerve fibres/axons which transmit action potentials to the CNS

Mediated by 3 types of Primary afferent fibres

  • Aβ = large myelinated (30-70m/s) touch, pressure, vibration (mechanoreceptors)
  • Aδ = small myelinated (5-30m/s) cold, “fast” pain, pressure
  • C = unmyelinated fibres (0.5-2m/s) warmth, “slow” pain

Proprioception is mediated by 2 types of primary afferent fibres:

  • Aα & Aβ eg muscle spindles, golgi tendon organs etc

ALL THESE FIBRES ENTER THE SPINAL CORD VIA THE DORSAL ROOT GANGLIA (OR CRANIAL NERVE GANGLIA FOR HEAD)

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6
Q

How do mechanoreceptive fibres (Aα & Aβ) transmit sensory information?

A
  1. Project straight up through ipsilateral dorsal columns
  2. Synapse in Cuneate & Gracile Nuclei
  3. 2nd order fibres cross over midline (decussate) in the brain stem & project to reticular formation, thalamus and cortex
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7
Q

How do thermoreceptive & nociceptive (Aδ & C) fibres transmit sensory information?

A
  1. Syanpse in the dorsal horn
  2. 2nd order fibres cross over the midline in the spinal cord
  3. Project up through the contralateral spinothalamic (anterolateral) tract to reticular formation, thalamus and cortex
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8
Q

How does damage to the dorsal column and anterolateral quadrant differ?

A

Dorsal column = mechano = cause loss of touch, vibration, propriception below lesion on ipsilateral side

Anterolateral quadrant = = thermoreceptive & nociceptive (pain) = loss of nociceptive and temperature sensation below lesion on contralateral side

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9
Q

Where does sensory information terminate?

A
  • Somatosensory cortex (S1) of the postcentral gyrus
  • Endings are grouped according to the location of the receptors
  • Extend of representation of location is related to density of receptors in each location = produces the sensory HOMUNCULUS on parietal lobe
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10
Q

What’s adaption in terms of processing sensory information; in terms of rapidly and slowly adapting?

A

Rapidly adapting: even with constantly high stimulus intensity, action potentials stop surpassing threshold - don’t respond to stimuli
= putting a hat on - you quickly forget and lose sensation

Slowly adapting: action potentials constantly breach threshold in response to the stimuli

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11
Q

What’s convergence and what are its drawbacks and benefits?

A

Convergence is where 1 postsynaptic cell receives convergent input from a number of different presynaptic cells - allows 1 neuron to communicate with numerous neurons in a network

Benefits: Reduces the number of neurons needed

Drawbacks: Reduces neural acuity (ability to distinguish between 2 individual signals

  • Underlies referred sensations
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12
Q

What’s the Specific ascending pathway in terms of convergence?

A
  • 2 receptors for touch OR 2 synapses for temperature synapse at the same post-synaptic cell – inability to distinguish between them = unable to tell where the high temp is actually coming from initially

Non-specific ascending pathway:
- Temperature and touch synapse at the same post-synaptic cell – unable to distinguish between the signals - just aware of something

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13
Q

What’s Lateral Inhibition?

A
  • Activation of 1 sensory input causes synaptic inhibition of its neighbours
  • Gives better definition of boundaries and cleans up sensory information
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14
Q

How does Lateral inhibition work?

A
  1. Stimulus on the skin (pin) detects pressure change etc
  2. Primary neuron response is proportional to stimulus strength (closest to pin contact = greater stimulus strength)
  3. Pathway closest to the stimulus inhibits neighbours
  4. Inhibition of lateral neurons enhances perception of stimulus
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15
Q

Why doesn’t all the sensory information reach the brain?

A
  • Higher brain centres possess descending controls; either excitatory or inhibitory neurons - can be pre OR postsynaptic
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16
Q

What’s Gate Control Theory of pain?

A

Its the theory that the activity of an opposing fibre can inhibit that of another

Inferred that non-nocieceptive fibres can interfere with nocieceptive signals

  1. Injury causes stimulation of (primary neurons) Fast pain Aδ fibres (myelinated) and slow C (non-myelinated) fibres which send action potentials and synapse in the Substantia Gelitanosa in the spinal cord
    - Cause release of Glutamate and Substance P which bind to post-synapase and lead to an action potential in the secondary neuron + ascends contralateral via the spinothalmic tract to the Thalamus
  2. Tertiary neuron extends to the Postcentral Gyrus in the Parietal lobe and the individual becomes aware of the pain
  3. Pain signals can be interrupted in the Substansia gelitanosa of the spinal cord which acts as a gate
  4. Non-painful stimuli such as deep touch activate Pacinian Corpuscle nerve endings which travel to the Substantia Gelitanosa via Dorsal-column medial lemniscal (DCML) system
  5. DCML activates inhibitory neurons which inhibit pain signals by secreting inhibitory-neurotransmitters such as Enkephalin which binds to opioid receptors on the axon terminal of primary neuron causing closure of calcium channels; reducing release of excitatory neurotransmitters = less excitation of secondary neuron and no hyperpolarisation