Basal Ganglia ppt 18 Flashcards

1
Q

What are the components of the basal ganglia?

A

Caudate Nucleus
Putamen
Globus Pallidus (external & internal)
Subthalamic Nucleus
Substantia Nigra (compact and Reticulata)

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2
Q

Where do inputs arrive in the basal ganglia?

A

at the stratum (caudate nuc and the putamen)

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3
Q

Where do outputs leave from in the basal ganglia?

A

from the internal globus

Sub. Nigra Reticulata

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4
Q

What is the purpose of the direct pathway?

A

Allows the thalamus to fire. Facilitates movement

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5
Q

What is the purpose of the indirect pathway?

A

To inhibit movement

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6
Q

What does a lesion of the Caudate Nucleus cause?

Head of the left caudate nucleus cause?

A

delayed alternation & disrupt performance on tests involving object reversal.

dysarthric aphasia (difficulty in articulating words)

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7
Q

What are the functions of the basal ganglia?

A
  • Planning and programing movement (preventing oscillations)
  • Slow and steady damp movement
  • inhibits stretch reflex
  • control of normal autonomic and associated movements (arms walking)
  • Striatum: sub. gross movement
  • GP:provides muscle tone for skilled movement
  • Sub Nigra: coordination of impulses for skilled movement.
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8
Q

What are movement disorders of the basal ganglia?

A

Bradykinesis, Hypokinesia, and Akinesia

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9
Q

Damage to the basal ganglia that results in increased resistant to passive movement

A

Rigidity.

Plastic, waxy or lead pipe rigidity

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10
Q

What is dystonia?

types?

A

distorted positions of the limbs

  • focal: torticollis,
  • blepharospasm: facial and eye muscles
  • spasmodic: laryngeal muscles
  • writer’s cramp.
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11
Q

Dystonia treatment

A

small amount of botulinum

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12
Q

What is Ballism?

A

Movements of the proximal limb muscles with a larger-amplitude,

hemiballismus,unilateral flinging of extremities

cause is a lacunar infarct of the subthalamic nucleus

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13
Q

What is athetosis?

A

writhing,twisting movements of the limbs, face, (choreoathetosis)

Causes: perinatal hypoxia, Wilson’s Huntington’s disease, and sever neonatal jaundice (kernicterus)

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14
Q

What is chorea?

A

Dance- continuous involuntary movement.

proximal, distal and respiratory muscles

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15
Q

Basal Ganglia dysfunction- Tics

A

sudden brief action preceded by urge.

motor, vocal (coprolalia- cursing)

Torrette’s syndrome: persistent

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16
Q

What is Parkinson’s?

A

Shaking palsy, resting tremor, bradykinesia, rigidity and unsteady gate

Path feature: Lewy bodies

17
Q

Causes of Parkinson’s

A
  • Idiopathic
  • Drugs: reserpine, phenothiazine
  • MMP: Methyl-phenyl-tetrahydropyridinum (MPTP), converted by MAO-B into methyl-phenyl-pyridinum (MPP)
  • Carbon monoxide
18
Q

Treatment of Parkinson’s

A
  • Levo-DOPA
  • Bromocriptine (dopa antagonist)
  • Anticholinergics
  • Selegilin (inhibits MAO-B)
  • Amantadine (anticholinergic)
  • COMT inhibitor (end in apone)
  • DBS
19
Q

What is Huntington’s?

A

Aut. Dominant
Abnormal movement and intellectual change (Chorea & Dementia)

caused by degeneration of GABAergic pathway

No Treatment- fatal

20
Q

What is a pathologic hallmark of Huntington’s

A

The pathologic hallmark is progressive atrophy of the striatum,especially involving the caudate nucleus.

21
Q

What is willsons?

A

Hepatolenticular degeneration.
abnormal copper metabolism.

personality change and athetoid movements

Kayser Fleisher ring

22
Q

What is Kernicterus?

A

increase indirect bilirubin– damage od GP– death