Week 9 - Motor Neurons and Movement Flashcards

1
Q

What are the 5 general steps involved in movement?

A
  • Plan movement
  • Initiate movement
  • Co-ordinate multiple muscles in space and time
  • Refine movements using sensory feedback
  • Optimise movements when repeated
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2
Q

Can one motor neuron innervate multiple muscle fibres?

A

yes
and each muscle fibre only receives input from one neuron

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3
Q

What are the 3 sources of input to LMNs?

A
  • Input from spinal interneurons
  • Sensory input from muscle spindle fibres
  • Input from UMNs in brain
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4
Q

Where are the cell bodies of LMNs found?

A
  • within brainstem of motor nuclei of cranial nerves
  • ventral horn of spinal cord
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5
Q

What are 2 descending pathways and what they do?

A

Corticospinal tract -> supplies musculature of body
Corticobulbar tract -> supplies musculature of head and neck

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6
Q

Distinction between lateral and anterior corticospinal tract?

A

Lat CST -> moves limbs and muscles contralaterally
Ant CST -> moves limbs in proximity to midline

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7
Q

What percentage of fibers decussate to form lateral CST? and how many remaining for anterior CST?

A

90% fibers cross at caudal medulla in a bundle of axons called pyrimidal decussation and form Lat CST

10% continue down ipsilaterally to form Ant CST

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8
Q

What are the motor systems involved in motor control? and how do they work in regard to motor function?

A

Posterior Parietal Cortex -> sens integration centre informing premotor cortex of sensory input

Prefrontal Cortex -> decision-making to execute action

Premotor Cortex -> receives info from prefrontal -> plans movement

Primary Motor Cortex -> receives info from pre-motor -> executes movement through muscle contraction and relaxation

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9
Q

What are the types of Unilateral Lesions and how do they affect the motor pathways?

A

UMN lesions above pyramidal decussation:
-> affect contralateral side

UMN lesions below pyramidal decussation:
-> affect ipsilateral side

LMN lesions:
-> produce ipsilateral paralysis and atrophy

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10
Q

What are symptoms of LMN lesions?

A
  • Loss of motor control (flaccid paralysis)
  • Weakness (Paresis)
  • Muscle fibres lose contractile proteins (muscle atrophy)
  • Loss of reflexes (Areflexia)
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11
Q

What are short and long-term symptoms of UMN lesions?

A

Short term:
- Flaccidity
- Hypotonia (less spinal cord activity
- Areflexia
Long term:
- Loss of fine movements
- Spasticity
- Babinski sign

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12
Q

What does the cerebellum do?

A

helps refine movements (planning movement // doesnt affect LMNs)

Functions:
- Gait coordination
- Maintenance of balance and posture
- Muscle tone control and voluntary muscle activity

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13
Q

What are the 3 functionally distinct cerebellar regions and what do they do?

A
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14
Q

What are symptoms of Cerebellar damage?

A

Ataxia -> uncoordinated movements
Dysenergia -> decomp of synergistic multi-joint movements (eg touching finger to nose)
Dysemetria -> lack of coordination -> results in overshoot/undershoot

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15
Q

Does cerebellum control ipsilateral or contralateral movements?

A

ipsilateral

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16
Q

What do the basal ganglia do?

A

modulate motor function and control movement

17
Q

What is the basal ganglia?

A

Interconnected nuclei below cerebral cortex

18
Q

What nuclei does the Basal Ganglia consist of?

A
  • Striatum (Caudate and Putamen)
  • Globulis pallidus
  • Substantia nigra
  • Subthalamic nucleus
19
Q

Direct and Indirect pathway of Basal Ganglia diagram

A

GPI = Globulis pallidus internal
-> this is inhibitory in nature so when you inhibit it via striatum, you are disinhibiting it therefore increasing stimulus to thalamus

20
Q

What are D1 and D2 expressing neurons and where are they?

A

D1-expressing neurons = excited by dopamine
D2-expressing neurons = inhibited by dopamine

21
Q

What produces dopamine?

A

Substantia nigra

22
Q

How does dopamine facilitate motor loops?

A
  • excites direct pathway
  • inhibits indirect pathway
23
Q

What happens when something goes wrong in basal ganglia like degeneration or lesion?

A

Disorders of Basal Ganglia characterised by limited or excessive movement.

Hypokinetic Disorders:
= overactivity in indirect pathway
- eg Parkinson’s

Hyperkinetic Disorders:
= underactivity of indirect pathway
- eg Huntington’s