Basal Ganglia Flashcards

1
Q

What does the basal ganglia consist of ?
(also called the extrapyramidal system
0

A

striatum (caudate and putamen), globus pallidus, substantia nigra, and the subthalamic nucleus

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2
Q

Hypokinesia

A

Parkinsons

motor activity is reduced or slowed, except for resting tremor

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3
Q

Hyperkinesia

A

choreoathetosis or hemiballismus

-excessive, involuntary movements

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4
Q

Parkinson’s disease

A

loss of dopaminergic neurons in the substantia nigra

-net increased inhibitory output of the GPm to the ventrolateral thalamic motor nuclei–reduction in stimulation of the motor cortex

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5
Q

Hemiballismus

A

destruction of the subthalamic nucleus

-net decreased inhibitory output of the GPm

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6
Q

Huntington’s disease

A

loss of indirect pathway putaminal neurons to the lateral globus pallidus

  • net decrease inhibitory output of GPm
  • -choreoathetosis
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7
Q

What are the clinical signs of Parkinson’s disease?

A

*1. resting tumor
-pill-rolling
*2. rigidity
cogwheeling
*3. bradykinesia
*4. impaired postural reflexes
-balance instability (light pushing)
5. masked facies
6. hypophonic speech-hoarse, soft and difficult to understand
7. micrographia
8. constipation, bladder dysfunction, or orthostatic hypertension
9. REM behavior sleep disorer

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8
Q

How is parkinson’s diagnosed?

A

clinically

  • at least 2 of the 4 primary clinical signs should be present and atypical features should be absent
  • improvement with first dopaminergic medication
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9
Q

What do you see in the neurons of parkinson’s?

A

loss of pigmented dopaminergic neurons in the substantia nigra
-alpha synuclein positive-Lewy bodies

grossly substantia nigra and locus ceruleus appear pale

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10
Q

Treatment of PD

A
  1. Levodopa-the most effective
  2. combined with carbidopa (limits catabolism of levodopa)
  3. COMT inhibitor -smoothes out undesirable motor fluctuations
  4. MAO type B inhibitor
    - extend effects of dopamine
  5. anticholinergic-control of resting tremor
  6. dopamine agonists

electrode into subthalamic nucleus to inhibiting it by means of repetitive electrical stimulation

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11
Q

Huntington’s disease

A

choreoathetosis, dementia, and behavior syndromes
-multiple trinucleotide repeats in huntingtin gene on chromosome 4

  • caudate atrophy and frontal horns of the lateral ventricles appear relatively enlarged
    treatment: dopamine antagonists and antidepressants and catecholamine depleter
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