lecture 15 - motor system 2 Flashcards

1
Q

What are some causes of hypotonia?

A

Motor neuron disease, polio, guillain-barre, cerebellar disease, muscle disease

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2
Q

What are the 3 types/locations of UMN lesions?

A

cortical, brain stem, spinal cord

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3
Q

What are the effects of a cortical UMN lesion?

A

UMN motor dysfunction, language/perceptual/cognitive dysfunction

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4
Q

What are the effects of a brain stem UMN lesion?

A

UMN motor dysfunction, cranial nerve deficits

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5
Q

What are the effects of a spinal cord UMN lesion?

A

UMN motor dysfunction, sensory pathway disruption

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6
Q

What are the key components of the basal ganglia?

A

internal capsule, striatum (caudate + putamen), globus pallidus,

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7
Q

What are the motor functions of the basal ganglia?

A

helps motor cortex select appropriate motor neurons for voluntary movement

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8
Q

What structure in the brain stem inhibits the basal ganglia, and via what neurotransmitter?

A

The susbtantia nigra, via dopamine

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9
Q

What are some examples of disorders of basal ganglia motor function?

A

Parkinson’s disease, Huntington’s disease

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10
Q

What is the typical age of onset of Parkinson’s disease?

A

45-70

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11
Q

What are the 5 key symptoms of Parkinson’s disease?

A

TRAPS:
Tremor (pill rolling)
Rigidity (lead pipe, cogwheel)
Akinesia/Bradykinesia (no/slow movement)
Postural Instability (forward leaning posture)
Shuffling Gait

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12
Q

What is the difference between a tremor in Parkinson’s vs a tremor from cerebellar dysfunction?

A

Parkinson’s tremor is present at rest, while in cerebellar dysfunction there is an intention tremor (tremor while trying to execute a function)

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13
Q

What is the rigidity symptom in Parkinson’s disease?

A

Sustained resistance to passive movements

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14
Q

What is the pathophysiology of Parkinson’s disease?

A

Death of dopaminonergic neurons in the substantia nigra, which lowers normal feedback to the striatum of the basal ganglia which is needed to contol voluntary movements.

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15
Q

What are the key drugs used in Parkinsons’ treatment?

A

Levo-dopa, Selegiline, Carbidopa

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16
Q

What is the mechanism of action of L-dopa for Parkinson’s disease?

A

Is a precursor of dopamine, which crosses the BBB and becomes dopamine, replacing levels lost in Parkinsons

17
Q

What is Huntington’s Disease?

A

An autosomal dominant neurodegenerative condition causing progressive death of neurons in the basal ganglia (caudate/putamen)

18
Q

What is the pattern of inheritance of Huntington’s disease?

A

Autosomal dominant, worsening with increasing CAG triplets on the Huntingtin gene with successive generations

19
Q

What are the symptoms of Huntington’s disease?

A

Chorea (excessive, random movements), dementia, agitiation, mania, paranoia, eventually loss of all voluntary movement

20
Q

What are the 3 regions of the cerebellum?

A

Spinocerebellum, cerebrocerebellum, vestibulocerebellum

21
Q

What does the spinocerebellar tract connect, and what information does it carry?

A

connects spinal cord with ipsilateral cerebellum, carrying afferent proprioceptive information from the body to assist in movement and posture of the trunks and limbs

22
Q

What does the cerebro/cortico cerebellar tract connect, and what information does it carry?

A

connects the cerebral cortex with the cerebellum, carrying efferent information for planning and integrating motor commands

23
Q

What does the vestibulocerebellar tract connect, and what information does it carry?

A

Connects the vestibular nerve to the cerebellum. Carries information for balance and eye movement.

24
Q

What are some of the general signs of cerebellar dysfunction?

A

Ataxia, hypotonia, intention tremor, gait abnormalities (staggering/lurching), nystagmus/double vision, dysdiadokinesia (inability to perform rapid alternating movements), dysmetria

25
Q

What are the key functions of the cerebellum?

A

Planning movements, motor learning