Anatomy and Physiology VII Flashcards

1
Q

What is the function of the direct pathway of the basal ganglia?

A

To facilitate movement (stimulatory) (p.416)

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2
Q

What is the function of the indirect pathway of the basal ganglia?

A

To inhibit movement (p.416)

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3
Q

Which dopaminergic receptors correspond to the direct and indirect pathways respectively?

A

Direct- D1; Indirect- D2 (p.416)

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4
Q

Describe the excitatory pathway through the basal ganglia.

A

Cortical inputs stimulate the striatum (putamen). This stimulates release of GABA. GABA release disinhibits the thalamus via the Gpi/SNr nuclei. This works to increase motion (p.416)

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5
Q

Describe the inhibitory pathway through the basal ganglia.

A

Cortical inputs stimulate the striatum (putamen). This disinhibits STN via the Gpe nucleus. STN then stimulates the Gpi/SNr nuclei to inhibit the thalamus. This decreases motion (p.416)

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6
Q

What is Parkinson’s disease?

A

A degenerative disorder of the CNS associated with Lewy bodies and loss of dopaminergic neurons (p.416)

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7
Q

What are Lewy bodies composed of?

A

A-synuclein intracellular inclusions (p.416)

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8
Q

What changes occur in the substantia nigra pars compacta due to loss of dopaminergic neurons in Parkinson’s disease?

A

Depigmentation (p.416)

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9
Q

What area of the brain is most affected by loss of dopaminergic neurons in Parkinson’s disease?

A

The substantia nigra pars compacta of the basal ganglia (p.416)

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10
Q

Name four clinical features of Parkinson’s Disease.

A

Resting tremor (“pill rolling tremor”); cogwheel rigidity; Akinesia (or bradykinesia); Postural instability (p.416)

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11
Q

What is the inheritance pattern of Huntington’s disease?

A

Autosominal dominant; trinucleotide repeat of CAG (p.417)

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12
Q

What neurotransmitters are decreased in the caudate nucleus of patients with Huntington’s disease?

A

GABA, Ach (p.417)

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13
Q

What are the clinical findings associated with Huntington’s disease?

A

Chorea, aggression, depression, dementia (p.417)

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14
Q

What is the pathophysiology associated with Huntington’s disease?

A

Neuronal death via NMDA-R binding and glutamate toxicity.

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15
Q

What imaging findings can be seen in a patient with Huntington’s?

A

Atrophy of the striatal nuclei (main inhibitors of movement) (p.417)

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16
Q

Name eight disorders of movement.

A

Hemiballismus; Chorea; Athetosis; Myoclonys; Dystonia; Essential Tremor (postural tremor); Resting tremor; Intention tremor (p.417)

17
Q

What is the characteristic presentation of Hemiballismus?

A

Sudden, wild flailing of 1 arm +/1 the ipsilateral leg (half of body typically affected) (p.417)

18
Q

What is the characteristic presentation of Chorea?

A

Sudden, jerky, purposeless movements (dance-like) (p.417)

19
Q

What is the characteristic presentation of Athetosis?

A

Slow, writhing movements, especially seen in fingers (p.417)

20
Q

What is the characteristic presentation of Myoclonus?

A

Sudden, brief, uncontrolled muscle contraction (common in metabolic abnormalities) (p.417)

21
Q

What is the characteristic presentation of Dystonia?

A

Sustained, involuntary muscle contractions (p.417)

22
Q

What is the characteristic presentation of Essential Tremor (postural tremor)?

A

Action tremor; exascerbated by holding posture/ limb position; genetic predisposition (p.417)

23
Q

What is the characteristic presentation of Resting Tremor?

A

Uncontrolled movement of distal appendages (most notable in hands) which is alleviated by intentional movement (p.417)

24
Q

What is the characteristic presentation of Intention tremor?

A

Slow, zigzag motion when pointing/ extending towards a target (p.417)

25
Q

What lesion is characteristically associated with Hemiballismus?

A

Contralateral subthalamic nucleus (e.g. lacunar stroke) (p.417)