Drugs - Dyskenesias - Huntingtons Flashcards

1
Q

Which is an inherited disorder characterized by progressive dementia?

A

Huntington’s Chorea

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2
Q

Where do the two aspects of Huntington’s, chorea and dementia, arise from?

A

chorea - striatal pathology

dementia - cerebral pathology

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3
Q

What is seen on the terminal of the HD gene in Huntington’s?

A

40+ repeats of CAG (the codon for glutamine)

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4
Q

At what age is Huntington’s usually seen?

A

30s or 40s (4th and 5th decades of life)

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5
Q

What is Huntington’s believed to be related to?

A

An imbalance of dopamine, acetylcholine, and GABA

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6
Q

What leads to the involuntary movements in Huntington’s?

A

The destruction of cholinergic neurons and GABAergic neurons in the striatum (indirect pathway) = overactivity of dopamine

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7
Q

What is thought to be the cause of impaired cognitive functions and dementia in Huntington’s?

A

The concomitant loss of cerebral cortex neurons

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8
Q

What drugs are used to treat Huntington’s?

A
  • Reserpine and tetrabenazine
  • Antipsychotics
  • alpha-methyl-p-tyrosine
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9
Q

What do reserpine and tetrabenazine do in the treatment of Huntington?

A

They deplete the dopamine stores in the CNS

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10
Q

What do antipsychotics do in the treatment of Huntington’s?

A

They block postsynaptic D2 receptors

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11
Q

What does alpha-methyl-p-tyrosine do in the treatment of Huntington’s?

A

It inhibits tyrosine hydroxylase so there is a decreased formation of dopamine

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12
Q

What is chorea exacerbated by?

A

Levodopa

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13
Q

What can low doses of dopamine agonist activate?

A

Presynaptic auto receptors which lead to inhibition of dopamine release

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