Basal Ganglia Flashcards
What does the basal ganglia consist of ?
(also called the extrapyramidal system
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striatum (caudate and putamen), globus pallidus, substantia nigra, and the subthalamic nucleus
Hypokinesia
Parkinsons
motor activity is reduced or slowed, except for resting tremor
Hyperkinesia
choreoathetosis or hemiballismus
-excessive, involuntary movements
Parkinson’s disease
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
Hemiballismus
destruction of the subthalamic nucleus
-net decreased inhibitory output of the GPm
Huntington’s disease
loss of indirect pathway putaminal neurons to the lateral globus pallidus
- net decrease inhibitory output of GPm
- -choreoathetosis
What are the clinical signs of Parkinson’s disease?
*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
How is parkinson’s diagnosed?
clinically
- at least 2 of the 4 primary clinical signs should be present and atypical features should be absent
- improvement with first dopaminergic medication
What do you see in the neurons of parkinson’s?
loss of pigmented dopaminergic neurons in the substantia nigra
-alpha synuclein positive-Lewy bodies
grossly substantia nigra and locus ceruleus appear pale
Treatment of PD
- Levodopa-the most effective
- combined with carbidopa (limits catabolism of levodopa)
- COMT inhibitor -smoothes out undesirable motor fluctuations
- MAO type B inhibitor
- extend effects of dopamine - anticholinergic-control of resting tremor
- dopamine agonists
electrode into subthalamic nucleus to inhibiting it by means of repetitive electrical stimulation
Huntington’s disease
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