Nervous system: The motor system Flashcards

1
Q

What is the effect of upper motor neurones on lower motor neurones?

A

They have a net inhibitory effect

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

What are the signs of lower motor neurone damage?

A
  • weakness
  • muscle wasting (LMN provides growth factors)
  • Areflexia or hyporeflexia
  • Fasciculation (ectopic Ach receptors)
  • Fibrillation
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

What are the signs of upper motor neurone damage?

A
  • weakness
  • Hypertonia
  • Hyper-reflexia (loss of inhibition)
  • Primitive reflexes return
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

What is the appearance of spasticity in an UMN lesion?

A

The upper limb is flexed and the lower limb is extended - this is due to the strongest agonistic muscle dominating eg bicep stronger than tricep so arm flexes

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

Name different types of rigidity

A
  • lead pipe
  • clasp knife
  • cogwheel
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

What causes lead pipe rigidity?

A

Parkinsons

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

What causes cogwheel rigidity?

A

Parkinsons

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

What causes clasp knife rigidity?

A

Spasticity caused by upper motor neurone lesions

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

What is the pathophysiology of parkinsons?

A

Degeneration of the substantia nigra which causes dopamine deficiency

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

What is the classical triad of symptoms seen in parkinsons?

A

Bradykinesia, tremor (pill-rolling and at rest) and rigidity (cogwheel)

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

What are some associated features of parkinsons?

A
  • Lewy body dementia
  • Smaller handwriting
  • Quiet voice
  • Mask-like facial expression
  • Anxiety and depression
  • Shuffling gait
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

What is the pathophsiology of huntingtons disease?

A

An autosomal dominant progressive disorder caused by cell loss in the basal ganglia and cortex

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

What is the age of onset of huntingtons?

A

30-50 years

Life expectancy is ~20 years after symptoms develop

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

What are the symptoms of huntingtons?

A
  • Chorea (abnormal unintentional movements)
  • incoordination
  • dystonia (abnormal tone)
  • cognitive decline
  • behavioural difficulties
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

What is the primary treatment for parkinsons? What are the associated side effects?

A

L-DOPA which is converted into dopamine via AADC - aromatic amino acid decarboxylase.
Excess dopamine in the periphery causes GI side effects such as nausea, anorexia

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

How can the side effects of parkinsons medications be reduced?

A

By giving Carbidopa.

Carbidopa inhibits aromatic amino acid decarboxylase in the periphery and therefore there is reduced dopamine.

17
Q

What are the pyramidal tracts?

A

Upper motor neurone tracts - the corticospinal (cortex to the spinal cord) and corticobulbar (cortex to brainstem). They control motor functions.
They pass through the pyramids of the medulla.

18
Q

What are the extrapyramidal tracts?

A

Tracts that do not pass through the medullary pyramids.

They are involved in the modulation and regulation of motor functions eg postural control, reflexes

19
Q

What are the basal ganglia?

A

A group of nuclei located at the base of the forebrain that are involved in motor function eg caudate nucelus, lentiform nucleus and substantia nigra.
Output of the basal ganglia is via the thalamus