Motor Tracts Flashcards

1
Q

What are the major motor tracts ?

A

Pyramidal tracts:
Corticospinal tract
Lateral
Anterior
Corticobulbar tract

Extrapyramidal tracts:
Tectospinal (colliulospinal) tract
Rubrospinal tract
Vestibulospinal tract
Reticulospinal tract

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

Explain the corticospinal tract

A

Main motor tract

Lateral tract:
Control of limbs
Decussation (crossing over) of in medullary pyramids

Anterior tract:
Control of axial muscles of trunk
Decussation of anterior tract (mostly) in spine near LMN synapses

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

Corticobulbar Tract

A

Control of voluntary face and neck movement

UMNs for cranial nerves, LMNs in brainstem nuclei

Travel to brainstem via ventral cerebral peduncles (crus cerebri)

LMNs exit via cranial nerves from brainstem

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

Rubrospinal Tract

A

Role in flexor muscle tone and co-ordination of reflexes;

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

Vestibulospinal Tract

A

Maintaining upright posture and reflexes (medial and lateral), head and head-eye co-ordination, vestibulo-ocular reflex.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

Reticulospinal Tract

A

Maintaining upright posture and reflexes (medial and lateral), head and head-eye co-ordination, vestibulo-ocular reflex.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

What is Amytrophic Lateral Sclerosis?

A

aka motor neurone disease, Lou Gehrig’s disease

Death of motor neurones (upper and lower)
Loss of co-ordination, weakness, slurred speech, eventually cognitive & behavioural deficits

90% sporadic (sALS), 10% familial (fALS). More common in athletes and highly active?

> 100 associated genes; most common familial form mutations in superoxide dismutase (SOD1)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

What is the treatment and lifespan for people withAmytrophic Lateral Sclerosis?

A

Lifespan from diagnosis usually 2-5 years

Riluzole – mechanism of action unclear, reduces Glu release
Delays need for ventilation and extends lifespan ~2-3 months

Novel therapies in clinical trials to prevent progression – some early results very promising, but only target some genetic forms

Mostly biologics (reduce neuroinflammation)

Stem cell treatments also examined

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

What are the lower motor nuerons ?

A

+ MAKE SURE I KNOW ALPHA AND GAMMA NUERONS.

BETA NUERONS NOT VERY IMPORTANT.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

What are muscle splindles

A

Extrafusal fibres (muscle) around outside

Intrafusal fibres (spindle) inside; these are small, non-contractile

Sensory neurones around the intrafusal fibres

Co-activation of α & γ:

Muscle contracts (α)

Spindle contracted (γ) to maintain tautness with muscle

Allows spindle to accurately report muscle contraction

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

Peripheral Motor Disorders

A
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

Some typical characteristics of peripheral motor disorders:

A

General weakness, hypotonia, hyporeflexia, fasciculations, stocking glove distribution

How well did you know this?
1
Not at all
2
3
4
5
Perfectly