Motor Control Flashcards

-> Organisation of the nervous system: Compare and contrast the structure of the central, peripheral and autonomic (sympathetic and parasympathetic) nervous systems -> Nervous system disorders: Describe the clinical features and treatment options of central and peripheral nervous system disorders

1
Q

What are the major descending tracts divided into?

A
  • Pyramidal tracts: Pass through the pyramids of the medulla
  • Extrapyramidal tracts: Do not pass through the pyramids of the medulla
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2
Q

What are the 2 pyramidal descending tracts?

A
  • Lateral corticospinal tract
  • Anterior corticospinal tract
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3
Q

What is the general path followed by the pyramidal tracts?

A
  • Motor cortex to spinal cord or cranial nerve nuclei in brainstem
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4
Q

What is the function of the pyramidal tracts?

A
  • Voluntary movements of body and face
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5
Q

What is the general path followed by the extrapyramidal tracts?

A
  • Brainstem nuclei to spinal cord
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6
Q

What is the function of the extrapyramidal tracts?

A
  • Involuntary (automatic) movements for balance, posture and locomotion
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7
Q

What type of tracts are the corticospinal and corticobulbar tracts?

A
  • Pyramidal tracts (major descending)
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8
Q

Outline the journey of the corticospinal tract until it divides into the lateral corticospinal tract and the anterior corticospinal tract (8 steps).

A
  1. Originate in the cell bodies of the first-order neurons in the primary motor cortex.
  2. The axons descend via through the cerebral peduncle of the midbrain.
  3. Through the ventral aspect of the pons to reach the ventral aspect of the medulla.
  4. At the medulla these fibres bundle together and create swellings known as the pyramids, and the majority of the corticospinal fibers cross over to the opposite side at the level of the caudal medulla, in what’s known as the pyramidal decussation.
  5. At this level, the corticospinal tract divides into the lateral corticospinal tract, and the anterior corticospinal tract.
  6. The decussated fibers form the lateral corticospinal tract, while the uncrossed fibers continue as the anterior corticospinal tract.
  7. The lateral corticospinal tract continues through the contralateral lateral column of the spinal cord, and synapse in the ventral horn on the lower motor neurons.
  8. The anterior corticospinal tract descends uncrossed within the anterior column, with its fibers decussating only after they reach the desired spinal cord level, where they synapse with lower motor neurons in the ventral horn.
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9
Q

What do the corticospinal tracts do? What are the corticospinal tracts responsible for?

A
  • The corticospinal tract is a motor pathway that carries efferent information from the cerebral cortex to the spinal cord
  • It is responsible for the voluntary movements of the limbs and trunk
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10
Q

What is the function of the lateral corticospinal tracts?

A
  • Innervate muscles of the limbs
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11
Q

Where does the corticobulbar tract originate?

A
  • Cell bodies of the upper motor neurones of the motor cortex
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12
Q

What is the function of the anterior corticospinal tracts?

A
  • Supply muscles of the trunks
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13
Q

What is the function of the corticobulbar tract?

A
  • Provides voluntary movements of body and face
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14
Q

What are the 4 extrapyramidal tracts?

A
  • Rubrospinal tract
  • Reticulospinal tract
  • Tectospinal tract
  • Vestibulospinal tract
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15
Q

Where does the vestibulospinal tract originate?

A
  • Originates in vestibular nuclei
    • ​Does not decussate
    • Synapses on interneurons in ventral horn of spinal cord
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16
Q

What is the funciton of the vestibulospinal tract?

A
  • Receives info about the position & motion of the head
  • Carries motor commands to extensor muscles of trunk & extremities
    • Helps maintain balance
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17
Q

Where does the reticulospinal tract originate?

A
  • Originates from reticular formation in pons & medulla
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18
Q

What is the function of the reticulospinal tract?

A
  • Excite or inhibit motor neurones to influence:
    • Voluntary movements
    • Posture
    • Reflexes
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19
Q

Where does the tectospinal tract originate?

A
  • Originates in suprior colliculi
    • ​Decussates
    • Synapses on intraneurones in ventral horns of cervical region
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20
Q

What is the function of the tectospinal tract?

A
  • Mediates postural reflexes of head & neck in reticuloendothelial system (RES)
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21
Q

Where does the rubrospinal tract originate?

A
  • Originates from red nucleus in midbrain
    • Decussates
    • Synapses within interneurons in ventral horn
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22
Q

Where does the rubrospinal terminate?

A
  • Cervical region
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23
Q

What is the function of the rubrospinal tract?

A
  • Regulates flexor & extensor muscle activity in upper limb (produces smoother & more coordinated movement)
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24
Q

What are the negative signs of an upper motor neuron (UMN) lesion (3)?

A
  • Loss of voluntary motor function
  • Paresis: graded weakness of movements
  • Paralysis (plegia): complete loss of voluntary muscle activity
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25
Q

What are the positive signs of an upper motor neuron (UMN) lesion (5)?

A
  • Increased abnormal motor function due to loss of inhibitory descending inputs
  • Spasticity: increased muscle tone
  • Hyper-reflexia: exaggerated reflexes
  • Clonus: abnormal oscillatory muscle contraction
  • Babinski’s sign
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26
Q

What is a Babinski reflex?

A
  • Sole of the foot is stimulated with a pointed instrument → hallux flexion (normal) or extension (sign of pathology)
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27
Q

What is apraxia?

A
  • A disorder of skilled movement. Patients are not paretic but have lost information about how to perform skilled movements
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28
Q

Which cerebral lobe lesions are commonly associated with apraxia?

A
  • Lesion of inferior parietal lobe, frontal lobe (premotor cortex and supplementary motor area)
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29
Q

Which motor areas are affected in apraxia?

A

Supplementary motor area (SMA) and premotor cortex

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30
Q

What is the function performed by the premotor cortex?

A

Concerned with movement planning and regulates externally cued movements

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31
Q

What area is responsible for planning internally cued movements?

A

Supplementary motor area

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32
Q

What are the most common causes of apraxia?

A

Strokes and dementia

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33
Q

What are the 6 main signs of a lower motor neurone lesion?

A
  • Weakness
  • Hypotonia (reduced muscle tone)
  • Hyporeflexia (reduced reflexes)
  • Muscle atrophy
  • Fasciculations
  • Fibrillations
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34
Q

What are fasciculations?

A
  • Damaged motor units produce spontaneous action potentials resulting in a visible twitch
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35
Q

What are fibrillations?

A
  • Spontaneous twitching of individual muscle fibres; recorded during electromyography examination
36
Q

What is the motor neurone disease (MND)?

A
  • Progressive neurodegenerative disorder of the motor system (upper and lower motor neurones)
37
Q

What is another term used to describe motor neurone disease (MND)?

A
  • Amyotrophic lateral sclerosis
38
Q

What are the upper motor neurone signs in motor neurone disease (MND) (6)?

A
  • Spasticity (Increased tone of limbs and tongue).
  • Brisk limbs and jaw reflexes
  • Babinski’s sign
  • Loss of dexterity
  • Dysarthria (Difficulty speaking)
  • Dysphagia (Difficulty swallowing)
39
Q

What are the lower motor neurone signs in motor neurone disease (MND) (5)?

A
  • Weakness
  • Muscle wasting
  • Tongue fasciculations and wasting
  • Nasal speech
  • Dysphagia
40
Q

What are the 7 main structures of the basal ganglia?

A
  • Caudate nucleus (C)
  • Putamen (P)
  • Globus pallidus (G)
  • Thalamus (T)
  • Nucelus accumbens (Acc)
  • Amygdala (Am)
  • Anterior commisure (AC)
41
Q

What are the functions of the basal ganglia (4)?

A
  • Decision to move
  • Elaborating associated movements (e.g. swinging arms when walking; changing facial expression to match emotions)
  • Moderating and coordinating movement (suppressing unwanted movements)
  • Performing movements in order
42
Q

What is the Parkinson’s Disease?

A
  • Degeneration of the dopaminergic neurons that originate in the substantia nigra and project to the striatum
43
Q

Which basal ganglia structure is predominantly affected in Parkinson’s disease?

A
  • Substania nigra
44
Q

What are the 5 main clinical presentations of Parkinson’s disease?

A
  • Bradykinesia
  • Hypomimic face
  • Akinesia
  • Rigidity (muscle tone increases, causing resistance to externally imposed joint movements)
  • Tremor at rest
45
Q

What is bradykinesia?

A
  • Slowness of small movements
46
Q

What is a hypomimic face?

A
  • Expressionless (absence of movements that normally animate the face)
47
Q

What is akinesia?

A
  • Difficulty in the initiation of movements because cannot initiate movements internally
48
Q

What is the Huntington’s Disease?

A
  • Degeneration of GABAergic neurons in the striatum, caudate and then putamen
49
Q

Which basal ganglia structures are affected in patients with Huntington’s disease?

A
  • Striatum
  • Caudate
  • Putamen
50
Q

What are the presenting symptoms in a patient with Huntington’s disease (5)?

A
  • Choreic movements (chorea) - rapid jerky involuntary movements of the body hands and face a
  • Speech impairment
  • Difficulty swallowing (dysphagia)
  • Unsteady gait
  • Later stages, cognitive decline and dementia
51
Q

What is the inheritance pattern of Huntington’s disease?

A
  • Autosomal dominant
52
Q

What type of mutation is inherited in a patient with Huntington’s disease?

A
  • CAG repeat
53
Q

What is ballism?

A
  • Sudden uncontrolled flinging of the extremities, symptoms occur contralaterally

Usually from stroke affecting the subthalamic nucleus

54
Q

Which basal ganglia structure is associated with Ballism?

A
  • Subthalamic nucleus
55
Q

Where is the cerebellum located?

A
  • Posterior cranial fossa
56
Q

Which structure separates the cerebrum from the cerebellum?

A
  • Tentorium cerebelli
57
Q

What is the main function of the cerebellum?

A
  • Coordinator and predictor of movement
58
Q

Which cerebellum structure is associated the regulation of gait, posture and equilibrium?

A
  • Vestibulocerebellum
59
Q

A tumour to the vestibulocerebellum can cause what type of symptoms (3)?

A
  • Gait
  • Ataxia
  • Tendency to fall
60
Q

What is the function of the spinocerebellum (3)?

A
  • Coordination of speech
  • Adjustment of muscle tone
  • Coordination of limb movements
61
Q

A lesion to the spinocerebellum can lead to what?

A
  • Abnormal gait and stance (wide-based)
    • Affects mainly legs
62
Q

Chronic alcoholism affects which part of the cerebellum?

A
  • Spinocerebellum
63
Q

Which cerebellar region is the most lateral?

A
  • Cerebrocerebellum
64
Q

What is the function of the cerebrocerebellum (5)?

A
  • Coordination of skilled movements
  • Cognitive function
  • Attention
  • Processing of language
  • Emotional control
65
Q

A lesion to the cerebrocerebellum affects what?

A
  • Arms / skilled coordinated movements (tremor)
  • Speech
66
Q

What are the main signs of cerebellar dysfunction (5)?

A
  • Ataxia
  • Dysmetria
  • Intention tremor
  • Dysdiadochokinesia
  • Scanning speech
67
Q

Define ataxia.

A
  • General impairments in movement coordination and accuracy: Disturbances of posture or gait: wide-based, staggering (“drunken”) gait
68
Q

Define dysmetria.

A
  • Inappropriate force and distance for target-directed movements (knocking over a cup rather than grabbing it)
69
Q

Define intention tremor.

A
  • Increasingly oscillatory trajectory of a limb in a target-directed movement (nose-finger tracking)
70
Q

Define dysdiadochokinesia.

A
  • Inability to perform rapidly alternating movements (rapidly pronating and supinating hands and forearms).
71
Q

Define scanning speech.

A
  • Staccato, due to impaired coordination of speech muscles.
72
Q

What is a motor unti?

A
  • A single motor neurone with all the muscle fibre that it innervates.
  • It is the smallest functional unit with which to produce force.

Fun fact: On average each motor neuron supplies about 600 muscle fibres

73
Q

What are the 3 types of motor units?

A
  • Slow (S, type I)
  • Fast, fatigue resistant (FR type IIA)
  • Fast, fatiguable (FF type IIB)
74
Q

How are the 3 different motor unit types classified?

A
  • Amount of tension generated
  • Speed of contraction
  • Fatiguability
75
Q

What are the two mechanisms by which the brain regulates the force that a single muscle can produce?

A
  • Recruitment
  • Rate coding
76
Q

What is recruitment when it comes to producing muscle force?

A
  • Smaller units are recruited first (these are generally the slow twitch units).
  • As more force is required, more units are recruited.

This allows fine control (e.g. when writing), under which low force levels are required.

77
Q

What is rate coding
when it comes to producing muscle force?

A
  • A motor unit can fire at a range of frequencies. Slow units fire at a lower frequency.
  • As the firing rate increases, the force produced by the unit increases.

Summation occurs when units fire at frequency too fast to allow the muscle to relax between arriving action potentials.

78
Q

Outline the monosynaptic reflex (3 steps).

A
  1. Tendon hammer causes stretch of the muscle
  2. Sensory neurone embeded within the muscle signals the CNS via the monosynaptic reflex
  3. Reflex contraction of the muscle
79
Q

What is the supraspinal control of reflexes?

A
  • The signal travels above the spinal cord before traveling back down to the same segment it entered the spinal cord from
    • Inhibitroy control dominates in normal condition
    • Excitatory control from supraspinal areas is visible only after cerebration
      • Can cause rigidity & spasticity
80
Q

What are the mechanisms of control of the supraspinal control of reflexes (5)?

A
  • Activating alpha motor neurones
  • Activating inhibiting interneurones
  • Activating propiospinal neurones
  • Activating gamma motor neurones
  • Activating terminals of afferent fibres
81
Q

How to increase the effect of the monosynaptic reflex?

A
  • Jendrassik manoeuvre
82
Q

What is the Jendrassik manoeuver?

A
  • Clenching the teeth, making a fist or pulling against locked fingers when having platella tendon tapped
  • Increases the reflexes speed & strength
83
Q

What are the signs of hyperreflexia (3)?

A
  • Overactive reflexes
  • Clonus
  • Babinski’s sign

Loss of descending (supraspinal) inhibition

84
Q

What is clonus?

A

Involuntary and rhythmic muscle contractions

Loss of descending inhibition

85
Q

What is the main cause of hyperreflexia?

A
  • Upper Motor Neurone (UMN) Lession
86
Q

What are the signs of hyporeflexia?

A
  • Below normal / absent reflexes
87
Q

What is the main cause of hyporeflexia?

A
  • Lower Motor Neurone (LMN) Lession