Motor Pathways Flashcards

1
Q

state the broad principles of motor control

A

Functional segregation and Hierarchical organisation

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2
Q

describe functional segregation

A

Motor system organised in a number of different areas that control different aspects of movement

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3
Q

describe Hierarchical organisation

A

high order areas of hierarchy are involved in more complex tasks (programme and decide on movements, coordinate muscle activity)

lower level areas of hierarchy perform lower level tasks (execution of movement)

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4
Q

Motor system hierarchy

A

(association cortex)
1) Motor Cortex: Receives info from other cortical areas and sends commands to brainstem and thalamus
2) Brainstem and Basal ganglia adjust commands fro other parts of motor system
3) Brainstem passes commands from cortex to spinal cord
(see diagram)

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5
Q

what is the location of Primary motor cortex

A

Primary motor cortex (M1):

Location: precentral gyrus, anterior to the central sulcus

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6
Q

what is the function of Primary motor cortex

A

Function: control fine, discrete, precise voluntary movement

Provide descending signals to execute movement

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7
Q

how is Somatotopical Organisation shown

A

This is called Penfield’s Motor Homunculus

In the motor cortex there is a representation of the muscles of different parts of the body

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8
Q

how is increased muscle use represented in the cortex

A

the more we use a muscle, the bigger the representation of that muscle in the cortex

The motor homunculus is very distorted because different parts of the body get used more than other parts

This is different in all of us - the cortical representation of the hand in a child is much smaller than that of a pianist

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9
Q

what are types of corticospinal tract

A

anterior and lateral

They are both composed of upper motor neurones

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10
Q

function of anterior corticospinal tract

A

The anterior tract is for axial UMNs

Axial: the muscles of the back and spine
Ie, UMNs supplying information to LMNs which will go on to innervate axial muscles

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11
Q

function of lateral corticospinal tract

A

The lateral tract is for appendicular UMNs

Appendicular: Muscles of the limbs

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12
Q

which neurones exit via the ventral root

A

Somatic and autonomic motor neurones

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13
Q

what order of neuornes exist in the corticospinal tract

A

Upper motor neurone
Cell body in the motor cortex in lamina V, betz cells
Axons travel in the lateral/ ventral corticospinal tracts to synapse with LMN.

Lower motor neurone
Cell body in the ventral horn
Axon travels out of the ventral root

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14
Q

describe the general path of upper and lower motor neurones before decussation

A

UMNs start in the motor cortex:

Path: corona radiata - internal capsule - peduncles at the midbrain

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15
Q

describe lateral corticospinal tract path

A

decussate in medullary pyramids
descend contralaterally in the lateral corticospinal tract
synapse with contralateral LMNs in the ventral horn

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16
Q

describe anterior corticospinal tract path

A

continue to descend ipsilaterally in the anterior corticospinal tract
decussate in the spinal cord at the anterior white commissure
Only then will they synapse with a LMN cell body in the ventral horn

17
Q

what percentage of neurones decussate in medulla and what type of neurones are they

A

90% (UMNs of lateral corticospinal tract)

10% that don’t cross over are of anterior corticospinal tract

18
Q

which other descending pathway is there and what does it do

A

Corticobulbar Tract - starts in the cortex, then exits and innervates the muscles in the face

19
Q

describe corticobulbar pathway

A

arise from the lateral aspect of the primary motor cortex - internal capsule - brainstem
neurones terminate on the motor nuclei of the cranial nerves (hypoglossal nucleus)
Here, they synapse with LMN (hypoglossal nerve), which carry motor signals to muscles of face and neck

20
Q

describe the location of the premotor cortex

A

frontal lobe anterior to M1

21
Q

describe the function of the premotor cortex

A

Function: planning of movements
Regulates externally cued movements
e.g. reaching out for an object:
moving a body part relative to another body part (intra-personal space)
movement of the body in the environment (extra-personal space)

22
Q

describe the location of the Supplementary motor area

A

frontal lobe anterior to M1, medially

23
Q

describe the function of the Supplementary motor area

A

Function: planning complex movements; programming sequencing of movements
Regulates internally driven movements (e.g. speech)
SMA becomes active when thinking about a movement before executing that movement

24
Q

briefly describe the association cortex and its constituants

A

Brain areas not strictly motor areas as their activity does not correlate with motor output/act
(Posterior parietal cortex and Prefrontal cortex)

25
Q

Role of posterior parietal cortex

A

ensures movements are targeted accurately to objects in external space
(part of association cortex)

26
Q

Role of posterior Prefrontal cortex

A

involved in selection of appropriate movements for a particular course of action
(part of association cortex)

27
Q

describe the timeline for Upper motor neuron lesion

A

Initially you get loss of function (‘negative signs’)

After a few weeks of having this lesion you will get increased abnormal motor function (‘positive signs’)

This is due to the loss of inhibitory descending inputs

28
Q

what are negative signs in UMN lesion

A

Paresis: graded weakness of movements

Paralysis (plegia): complete loss of muscle activity

29
Q

what are positive signs in UMN lesion

A

Spasticity: increased muscle tone
Hyper-reflexia: exaggerated reflexes
Clonus: abnormal oscillatory muscle contraction
Babinski’s sign

30
Q

what is Babinski’s sign

A

important sign of an upper motor lesion

If you stroke the plantar side of the foot, the toes will flex and the big toe will also flex (in a normal subject) but after upper motor neurone lesions the toes will fan and the big toe will go up

Also called the extensor plantar response

31
Q

what is Apraxia

A

A disorder in skilled movement NOT caused by weakness, abnormal tone or posture or movement disorders (tremors or chorea)

Patients are NOT paretic (partial motor paralysis) but have lost information about how to perform skilled movements

32
Q

what causes Apraxia

A

Lesion of inferior parietal lobe, the frontal lobe (premotor cortex, supplementary motor area)

Any disease of these areas can cause apraxia, although stroke and dementia are the most common causes

33
Q

what is a LMN lesion

A

Affects the second motor neurone (the one that starts in the grey matter of the spinal cord and exits to form peripheral nerves)

Lower motor neurone lesions have the opposite set of signs to upper motor neurone lesions

34
Q

what are signs of LMN lesion

A
Weakness 
Hypotonia (reduced muscle tone) 
Hyporeflexia (reduced reflexes)  
Muscle Atrophy - the metabolic trophic support lost  
Fasciculations  
Fibrillations
35
Q

what is a fasciculation

A

damaged motor units produce spontaneous action potentials, resulting in a visible twitch

36
Q

what is a fibrillation

A

twitch of individual muscle fibres - these aren’t visible to the naked eye but can be recorded if the patients have needle electromyography

37
Q

what is Motor Neuron Disease (MND)

A

Progressive neurodegenerative disorder of the motor system
Spectrum of disorders

MND can affect only UMNs, only LMNs or both

When MND affects both UMNs AND LMNs it is called Amyotrophic Lateral Sclerosis (ALS)

38
Q

Upper motor neuron signs of MND

A
Increased muscle tone (spasticity of limbs and tongue)
Brisk limbs and jaw reflexes 
Babinski’s sign
Loss of dexterity
Dysarthria
Dysphagia
39
Q

Lower motor neuron signs of MND

A
Weakness
Muscle wasting
Tongue fasciculations and wasting
Nasal speech
Dysphagia