34 - Reflexive and Voluntary Activation of Muscle Flashcards

1
Q

Location of motor neurons in the spinal cord

A

Ventral horn (form clusters)

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2
Q

Number of motor neurons innervating each muscle

A

Hundreds to thousands

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3
Q

Number of fibres within a muscle innervated by a single motor neuron

A

Each MN will innervate several muscle fibres (will split, form several motor endplates)

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4
Q

Is the activation of muscles graded?

A

Not really. Largely binary - muscle fibre will either contract or not.

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5
Q

Relationship between size of motor unit and power and fineness of movement

A

The more fibres involved in a motor unit, the greater force it will lead to.
A lot of motor units -> powerful movements, easier to fatigue
Fewer motor units -> finer movements, harder to fatigue.

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6
Q

Morphology of a neuromuscular junciton

A

Synaptic membrane of the neuron has varicosities, to increase surface area.
Post-synaptic membrane is heavily-folded, also to increase surface area.

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7
Q

Three phenomena that arise if muscles remain unactivated

A

1) Fibrillation
2) Fasciculation
3) Atrophy and degeneration

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8
Q

Fibrillation

A

Tiny contraction cause by activity of a single muscle cell - can be due to hypersensitivity, increased AChr expression (including extra-junctional), activation is not synaptic thus not summated.

Extra-junctional twitches from increased AChR expression, which makes muscle fibres more sensitive to ACh from outside neuromuscular junction

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9
Q

Fasciculation

A

groups of muscle fibres contracting involuntarily, probably a
motor unit synaptically activating due to spontaneous activation of a degenerating MN / axon. Can be measured on surface (cf. fibrillations - need extracellular electrode).

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10
Q

Atrophy and degeneration

A

Long term denervation: atrophy and degeneration.
Atrophy can occur in catabolic stares (diabetes, Cushing’s disease) but complete denervation will lead progressively to irreversible muscle loss.

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11
Q

Structure involved in monosynaptic stretch reflex

A

Muscle spindle.

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12
Q

Signs, symptoms of lower motor neuron lesions

A
Weakness or paralysis
Decreased superficial reflexes
Hypoactive deep reflexes
Decreased tone
Fasciculations, fibrillations
Severe muscle atrophy
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13
Q

Difference between superficial and deep reflexes

A

Superficial - EG withdrawal from a noxious stimulus

Deep - EG monosynaptic stretch reflex

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14
Q

Two regions of the spinal white matter where upper motor neurons from brain descend to lower motor neurons

A
Lateral pathways (EG corticospinal tract) (mostly control distal muscle)
Ventromedial pathways (mostly control proximal muscle)
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15
Q

Broad descending motor tract layout (ventromedial)

A

Originate in motor and premotor cortices
Descend ipsilaterally through brainstem.
Some fibres cross over in pons, some don;t
Descend through reticular formation

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16
Q

Lateral corticospinal tract

A

Begin in motor cortex
Descend through cerebral peduncle, middle pons, middle medulla (both with collaterals to reticular formation), decussate at pyramidal decussation.

17
Q

Three main ventral tracts (involved in maintenance of posture)

A
Lateral and medial vestibulospinal tracts (involved in balance)
Reticulospinal tract (initiating movements)
Colliculospinal tract (orienting movements, EG changing position to a stimulus, such as a noise)
18
Q

Function of most primary motor neurons

A

Inhibitory of lower motor neurons.

If removed, lower motor neurons become hyper-excitable (increased spinal reflexes, increased muscle tone)

19
Q

Signs and symptoms of upper motor neuron syndrome

A

Weakness
Spasticity (increased tone, hyperactive deep reflexes, clonus)
Babinski’s sign
Loss of fine voluntary movements