Spinal cord compression - 129 Flashcards

1
Q

Where do afferent neurons conduct to/from?

A

Conduct signals from sensory receptors INTO the CNS

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2
Q

Where do efferent neurons conducts to/from?

A

Conduct motor/effector signals from the CNS OUT to effectors, e.g. muscle

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3
Q

What is a ganglion?

A

A collection of neurons usually located outside the brain

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4
Q

What are the 5 components to each reflex circuit? (Regarding spinal reflexes)

A

1) sensory receptor 2) afferent path to CNS 3) synapse within CNS 4) efferent path from CNS 5) effector

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5
Q

What do inhibitory interneurons in the spinal cord allow for?

A

Contraction of agonist and simultaneous relaxation of the antagonist

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6
Q

Which root does sensory information pass through?

A

Dorsal root

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7
Q

Efferent information passes through which root in the spinal cord?

A

Ventral

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8
Q

What do muscle spindles do?

A

Detect changes in muscle length, stretch generates an action potential.

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9
Q

What is a myotatic reflex? What is the function of this reflex?

A

Stretch reflex.
Muscle lengthens -> muscle spindle is stretched and its nerve activity increases. Increases alpha motor neuron activity -> muscle fibers contract and resist stretching.
A secondary set of neurons causes opposing muscle to relax.
The reflex functions to maintain the muscle at a constant length.

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10
Q

What does tetanus toxin do?

A

Inhibit glycine release

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11
Q

What is responsible for making you drop heavy things? Why does this happen?

A

Golgi tendon organ. Has a higher threshold than muscle spindle and is activated by prolonged stretch, Ib afferent. Activation produces inhibition of homonymous muscle, preventing tendon damage

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12
Q

Do alpha motor neurones cause muscle contraction or spindle contraction?

A

Muscle contraction. The spindle is flaccid.

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13
Q

What causes muscle spindle contraction? What is the purpose of this?

A

Gamma motor neurons. It regenerates tension in the muscle

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14
Q

What cells are involved in recurrent inhibition?

A

Renshaw cells.

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15
Q

What are Renshaw cells?

A

inhibitory interneurones found in gray matter of spinal cord -> associated with an alpha motor neurone. They are excited by a-motor neurone, release glycine back onto the motor neurone, thus inhibiting firing. This allows synergistic muscles to contract together.

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16
Q

Where does descending motor control originate?

A

Pyramidal cells of motor cortex

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17
Q

What is apraxia?

A

Inability to produce a specific motor act even though sensory and motor pathways are intact - e.g. cannot execute a movement on request.

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18
Q

Name 2 descending tracts

A

Corticobulbar and corticospinal

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19
Q

What is the anterolateral system?

A

Ascending pathway that comprises 3 main pathways

20
Q

What are the 3 main pathways of the anterolateral system?

A

Spinothalamic, spinoreticular and spinotectal

21
Q

What are some classic signs and symptoms of a LMN lesion?

A

Hyporeflexia, fasiculations, muscle atrophy, denervation.

22
Q

What are some classic signs and symptoms of an UMN lesion?

A

Paralysis, hyperreflexia, increased muscle tone, spasticity, babinski relex, bladder, bowel and sexual dysfunction

23
Q

Where do corticospinal fibres most commonly decussate?

A

At the junction of the medulla and spinal cord

24
Q

Where do fibres of the spinothalamic tract most commonly decussate?

A

In ventral white commissure. Pain and temperature axons usually cross within 1 segment of origin. Touch and pressure may ascend several segments before crossing.

25
What is Brown-sequard syndrome?
Any presentation of spinal injury that is an incomplete lesion (hemisection)
26
A hemisection of the spinal cord will result in a loss of touch, pain, temperature and pressure where?
On the opposite/contralateral side of the lesion.
27
What is cauda equina syndrome?
Compression of lumbar and sacral nerve roots within the cauda equina
28
How might a patient with cauda equina syndrome present?
Red flags are: urinary retention, faecal incontinence, saddle anesthesia, pain on straight leg raise, weakness of ankle plantar and dorsi flexion
29
What is complex about a patient with amytrophic lateral sclerosis when regarding signs/ symptoms?
They will have a mixture of UMN and LMN signs/symptoms. It is a motor neurone disease
30
How might a patient with ALS present?
Dysarthria, slow tongue movements, brisk jaw jerk, weakness, wasting, fasiculations
31
What is motor neurone disease?
Disease causing wasting of the anterior horn cells with resulting upper and lower mostor neuron symptoms
32
What cells are lost in motor neurone disease?
Anterior horn cells
33
How might you treat motor neurone disease?
Palliatively, there is no effective treatment. Riluzole can increase life expectancy by 3 months
34
What is myasthenia gravis?
An acquired autoimmue disease with antibodies against nicotinic ACh receptors at the neuromuscular junction.
35
What are the main symptoms someone with myasthenia gravis will suffer from?
Muscle weakness and fatigue
36
Which muscles are more affected in Myasthenia gravis? (Proximal or distal)
Proximal
37
What other condition/abnormality is myasthenia gravis often associated with?
Thymus abnormalities.
38
What investigations would be done if you expected a patient to have myasthenia gravis?
Serology -> ACh and Muscarinic antibodies. Neurophysiology, Edrophonium test (a reversible aceytlcholineesterase inhibitor) Could also do the peek test
39
How would myasthenia gravis be treated?
ACh esterase inhibitors, immunosuppressive drugs, Ab treatment, ?surgery
40
Where would a transection of the spinal cord need to be to cause quadraplegia?
At the cervical regions
41
Paraplegia is a result of a transection of what area of the spinal cord?
Below cervical regions
42
What is the term for weakness in 1 limb?
Monoparesis
43
Radiculo- pertains to what?
nerve root
44
How would you describe paralysis of both legs?
Paraplegia
45
Hemiplegia describes what?
Paralysis of 1 side
46
Quadraparesis describes what?
Weakness of 4 limbs