Basic neurology & disease Flashcards

(57 cards)

1
Q

What does an afferent neurone do?

A

Carries information from sensory receptors into the CNS.

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2
Q

Where do afferent neurones enter the CNS?

A

Through dorsal root ganglia.

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3
Q

What does an efferent neurone do?

A

Carries motor signals from the CNS to effector muscles.

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4
Q

Where do efferent neurones leave the CNS?

A

Thought ventral root ganglia.

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5
Q

What is a ganglion?

A

A collection of neurones or cell bodies of neurones outside the CNS.

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6
Q

What do muscle spindles detect?

A

Muscle stretch.

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7
Q

What neurones do muscle spindles cause APs in?

A

1a afferent neurones.

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8
Q

What do 1a afferent neurones innervate?

A

Alpha motor neurones & inhibitory interneurones.

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9
Q

What do golgi tendons detect?

A

Muscle tension.

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10
Q

What neurones doe golgi tendons cause APs in?

A

1b afferent neurones.

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11
Q

What does two actions result from activation of the muscle spindle?

A

Excitation of alpha motor neurone projecting to the homonymous muscle > contraction of the homonymous muscle.

Excitation of the inhibitory interneurone > inhibition of the alpha motor neurone projecting to the heteronymous muscle > relaxation of the heteronymous muscle.

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12
Q

What are renshaw cells & what is their role?

A

Inhibitory neurones which release glycine onto alpha motor neurones to make the spinal reflex transient.

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13
Q

What does tetanus inhibit?

A

Glycine release.

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14
Q

Explain the myotactic reflex?

A

Stretch of a muscle > stretch of the muscle spindle > AP in 1a afferent neurone > activation of the alpha motor neurone projecting to the homonymous muscle > contraction of the homonymous muscle.

The 1a afferent neurone also activates the inhibitory interneurone projecting to the alpha motor neurone of the heteronymous muslce > relaxation of the heteronymous muscle.

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15
Q

Explain the inverse myotactic reflex?

A

Increased muscle tension > activation of the GTO > AP in 1b afferent neurone > excitation of inhibitory interneurone > inhibition of the alpha motor neurone projecting to the homonymous muscle > relaxation of the homonymous muscle.

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16
Q

What are synergistic muscles?

A

Muscles that contract together to produce the same movement.

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17
Q

What is the role of gamma motor neurones?

A

Ensure the muscle spindle is always kept under tension.

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18
Q

What are the most important tracts for voluntary movement?

A

Corticospinal tracts.

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19
Q

Where do corticospinal tracts originate?

A

Pyramidal cells of the motor cortex.

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20
Q

Where do corticospinal tracts decussate?

A

At the decussation of the pyramids in the medulla.

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21
Q

Where is the premotor area found & what is its role?

A

Found in the frontal lobe.

Required for the planning of movements & movements that require visual guidance.

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22
Q

Where is the primary somatosensory cortex found & what is its role?

A

Found in the parietal lobe.

Required for filtering out of irrelevant sensory information.

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23
Q

Where is the supplementary motor area found & what is its role?

A

Found in the frontal lobe.

Required for coordinating voluntary movements.

24
Q

What is anosognosia?

A

Unawareness of a disability.

25
Damage to which area may result in anosognosia?
The posterior parietal cortex.
26
What is apraxia?
Inability to produce a specific motor act even though sensory & motor pathways are intact.
27
Damage to which areas result in apraxia?
Primary motor cortex. Supplementary motor area. Posterior parietal cortex.
28
What are the two types of apraxia?
Ideomotor apraxia: > Cannot execute a specific movement on request even though the movement is known. Ideational apraxia: > Cannot conceptualise the movement.
29
What information does the lateral spinothalamic tract carry?
Pain & temperature.
30
What information does the dorsal column carry?
Proprioception & soft touch.
31
What are the classic signs of a UMN lesion?
Hyper-reflexia. Spasticity. Postivie babinski reflex.
32
What are the classic signs of a LMN lesion?
Hypo-reflexia / areflexia. Fasiculations. Muscle atrophy.
33
Where does the lateral spinothalamic tract decussate?
At the level is enters the spinal cord.
34
What level does the dorsal column decussate?
At the level of the medulla.
35
What is Brown-Sequard syndrome?
Lateral hemisection of the spinal cord.
36
What are the signs of Brown-Sequard syndrome?
Loss of motor function on the ipsilateral side at the level of & below the lesion. Loss of proprioception & soft touch on the ipsilateral side at the level of & below the lesion. Loss of pain & temperature sensation on the contralateral side at the level of & below the lesion.
37
What are the causes of spinal cord disease?
``` Trauma. Infection. Demyelination (i.e. MS). Compression. B12 deficiency. Anterior spinal artery infarction. Inflammatory (i.e. SLE). ```
38
What does paresis mean?
Weakness.
39
What does plegia mean?
Paralysis.
40
What does myelo mean?
Pathology of the spinal cord.
41
What does radiculo mean?
Pathology of the nerve root.
42
What does neuro mean?
Pathology of the peripheral nerves.
43
What does myo mean?
Pathology of muscle.
44
What are the functions of UMN pathways?
Dampening of the reflex arc. Suppressing muscle over-activity & spasm. Suppressing primitive reflexes (i.e. babinkski).
45
What is a LMN?
anterior grey horn cell.
46
What is a UMN?
Anything above the synapse of the anterior grey horn cell.
47
What are the classic signs of muscle disease?
Proximal muscle weakness & pain. Muscle wasting or hypertrophy. Normal reflexes. Raised CK.
48
What is papilloedema & what does it suggest?
Swelling of the optic nerve - suggests raised ICP.
49
What is dysarthia?
Difficulty with speech articulation.
50
What pathways degenerate in motor neurone disease?
UMN: > corticospinal tracts. > corticobulbar tracts. LMN: > loss of anterior horn cell.
51
What are the signs of motor neurone disease?
Hyper-reflexia. Pseudobulbar palsy. Fasiculations. Elevated CK.
52
What drugs can cause muscle disease?
Statins. Steroids. Anti-virals. Chloroquine.
53
What are the signs of polymyositis?
Proximal muscle weakness.
54
What are the signs of dermatomyositis?
Promxial muscle weakness. Rash over hands & face. Mainly in adults with malignancy.
55
What are the signs of inclusion body myositis?
Proximal leg muscle & long finger flexor weakness. | Mainly in the elderly.
56
What is cauda equina syndrome?
Compression of the cauda equina.
57
What are the symptoms of cauda equina syndrome?
``` Bilateral sciatica. Saddle & genitalia anaesthesia. Sphincter & sexual dysfunction. Loss of ankle reflexes. Leg weakness & pain on raising. ```