Somatic and visual sensation Flashcards

1
Q

What is the difference between rapidly and slow adapting units?

A

Rapidly adapting units initially fire with high frequency, but then frequency of impulses decrease even though the receptor continues to be stimulated. This means we lose conscious perception of irrelevant stimulus (example of these are cutaneous mechanorecpetors).
Slow adapting units will never decrease the frequency of impulses (examples of these are pain receptors)

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2
Q

What is a receptive field?

A

The area of skin that one sensory nerve innervates. Receptive fields tend to overlap- means dermatomes have ‘fuzzy’ boundaries.

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3
Q

How is the size of the receptive field related to sensory acuity of that area.

A

Smaller the receptive field the greater the acuity. (acuity proportional to 1/ size of receptive field)

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4
Q

Describe the dermatomal organisation of neurones in the dorsal column and spinothalamic pathways?

A

Doral column- C4 located laterally, S5 medially

Spinothalamic- C4 located proximally (to grey matter/ canal), S5 located distally

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5
Q

What modalities are sensed by the dorsal column and the spinothalamic pathways?

A

dorsal column- light tough, proprioception, vibration and 2 point discrimination
Spinothalamic- pain, tempreature, crude touch

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6
Q

Describe the path and locations of cell bodies of the primary, secondary and tertiary neurones of the dorsal- column- medial-lemniscus pathway

A

Primary- cell body found in dorsal root ganglion, axon travels up dorsal column (no decussation)
secondary- cell body of upper limb neurones found in cuneate nucleus, cell body of lower limb found in nucleus gracillis (both medulla). Axons follow medial lemniscus pathway to thalamus
Tertiary- cell body in thalamus projects to relevant area of sensory homunculus in parietal lobe

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7
Q

Where will the sensory deficit be if there is an isolated lesion of the right dorsal column in the spinal cord?

A

the ipsilateral side- as doesn’t decussate until the medulla

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8
Q

Why may some vegans get bilateral loss of light tough, proprioception, vibration and two point discrimination across 2/3 dermatomes?

A

B12 deficiency can lead to demyelination of the dorsal column, often bilateral and affects a couple of levels. the demyelination can usually be seen with an MRI.

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9
Q

Describe the path of the spinothalamic pathway

A

Primary sensory neurone cell body found in DRG. Axon enters dorsal horn at same level as enters spine.
Secondary neurone cell body in dorsal horn. Axon travels anteriorly and decussates at the white commissure (white matter between the two ventral horns), axons ascends to thalamus.
Tertiary sensory neurone cell body found in thalamus. Axons travel to relevant area of motor homunculus.

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10
Q

What is syringomyelia? What will it present with?

A

A cyst in the white commissure of the spinal cord. Leads to bilateral loss of pain, temp and crude touch. Number of dermatomes affected depends on how long it is and the level it appears at. If width increases it may affect other structures. They usually occur in C spine.

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11
Q

Describe the difference in presentation between sharp cord transections and large lesions- eg due to crushing.

A

Sharp transections- ascending and descending neurones cut but relatively little grey matter and LMNs destroyed- means reflexes may still be intact.
Crushing injuries more devastating as grey matter lost as well as white + LMN loss = areflexia

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12
Q

Explain the presentation of brown- sequard syndrome?

A

One half of spinal cord transected:

  • Complete ipsilateral loss of affected dermatome as dorsal root and horn is lost)
  • Ipsilateral loss of dorsal column (light tough, vibration etc) as this doesn’t decussate till medulla
  • Contralateral loss of spinothalamic - as this decussates at level of associated spinal nerve
  • Ipsilateral UMN signs as corticospinal tract cut, LMN signs at level of lesion and initially due to spinal shock
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13
Q

What is the descending control of pain?

A

Where fibres descending from the periaqueductal grey area of the midbrain are able to inhibit transmission of pain stimuli from primary to secondary neurones via release of serotonin and enkephalin. This means you can psychologically block pain.

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14
Q

Why does rubbing a sore bit stop it hurting

A

Gating of pain:
Mechanoreceptors stimulation leads to inhibition of primary to secondary transmission of pain via stimulation of an interneurone which releases enkephalin.

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15
Q

Give 3 causes of insensitivity to pain?

A

diabetic neuropathy, congenital insensitivity to pain, leprosy

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16
Q

Describe how light stimuli are transmitted to the optic nerve?

A

Light detected by rods and cones, which synapses with bipolar cells (infront of the rods and cones), which synapses with the ganglionic cells (infront of bipolar cells), axons of ganglionic cells travel to optic nerve.

17
Q

What is the macula?

A

The area with the highest density of cones, there is also a dip here called the fovea centralis which is where the neural layer is thinner so light can more easily travel through it, both of these things leads to higher acuity vision.

18
Q

Why do we have a blind spot?

A

At the optic disc there are no photoreceptor cells.

19
Q

What is amaurosis fugax?

A

the result of a retinal artery occlusion, it is described as seeing a curtain come down over your vision

20
Q

Describe the visual pathway

A
  • Nasal fibres decussate at optic chiasm
  • Temporal fibres stay ipsilateral
  • Optic tract runs into lateral geniculate nucleus
  • superior nasal and temporal fibres come together to form superior radiation which travels through parietal lobe to primary visual cortex
  • inferior nasal and temporal fibres come together to form inferior radiations which go through temporal lobe to primary visual cortex
21
Q

whats the difference between the optic nerve and optic tact?

A

Optic nerve is before chiasm optic tract is after chiasm

22
Q

Describe the presentation and location of lesion causing monocular blindness? Give 2 causes?

A

Complete loss of vision in one eye.
Caused by ipsilateral lesion of optic nerve, may be due to glioma or retinoblastoma in children or optic sheath meningiomas in middle aged ppl.

23
Q

Pt lost lateral half of vision in both eyes (has tunnel vision). What is name for this and what is cause

A

Bitemporal hemianopia
Lesion of optic chiasm- loss of all nasal fibres = loss of peripheral fields of vision. Usually due to pituitary tumour, raised ICP, dilation of anterior communicating artery.

24
Q

Pt has lost medial feilds of vision in right eye and lateral feilds of vision in left eye.
Name deficit and describe cause

A

Left homonymous hemianopia.
Loss of temporal fibres in right eye and nasal fibres in left eye= lesion of right optic tract. Often due to strokes, but also neoplasms and trauma.

25
Q

Pt presents with loss of both left lower visual field quadrants.
Name the deficit and describe the cause?

A

Lost superior temporal from right eye and superior nasal from left eye.
Lesion is therefor at right superior radiation

26
Q

Describe and explain the cause of a left homonymous hemianopia with macula sparing?

A

Stroke has affected the posterior cerebral artery, effectively disabling the right superior and inferior radiations.
However the occipital pole (which represents the macula) has dual blood supply from the middle cerebral artery so the macula (central vision) will be spared.

27
Q

Describe the pathway of the light reflex?

A
  • light stimulates optic nerve
  • axons travel to occipital lobe and synapses in pretectal area
  • this gives rise to neurones going to both edinger westphal nuclei
  • Each EWN is stimulated (even if light only detected by one eye) and so parasympathetics of both oculomotor nerve are stimulated.
28
Q

What are the three aspects of accommodation reflex

A
  • convergence (medial rectus)
  • pupil constriction (constrictor pupillae)
  • convexity of lens (cillary muscles contract)
29
Q

Describe the accomodation reflex pathway?

A
  • follows visual pathway to LGN where a neurone synapses and goes to visual cortex
  • info is interpreted and synapses with a fibre going to the pretectal area
  • which stimulates EDW nucleus
  • which stimulates occulomotor nerve
30
Q

Give 3 causes of perception of excessive glare?

A

Cateracts
Uveitis
Albinism
Anything causing more scattering of light in eyeball

31
Q

what happens in MLF syndrome/ inter nuclear opthalmoplegia?

A

On looking left or right with the adducting eye ball lags behind the adbucting eyeball, presents with diplopia

32
Q

describe the pathophysiology of MLF syndrome

A

1-lesion to medial longididunal fasciculs (MLF)
2-the MLF normally connects CNVI nucleus to CNIII nucleus to coordinate movement of the lateral rectus and the medial rectus on looking left and right
3-Therefore MLF lesion = medial rectus lags behind lateral rectus

33
Q

why is the function of the medial rectus normal during convergence of someone with MLF syndrome?

A

because the medial rectus and oculomotor nerve themselves are fine

34
Q

what will be the result of a tumor arising from the cerebral aqueduct of the mid brain?

A

as it grows it will impinge EDW nucleus first impinging pupil constriction, lens flattening and pupillary light reflex. Further growth = CNIII nucleus lesion causing ptosis down and out eye and loss of convergence plus blown pupil.

35
Q

What is amaurosis fugax?

A

Occlusion of the central retinal artery or ophthalmic artery leading to transient blindness, described as curtain coming down over vision