Physiology - Basal Ganglia Flashcards

1
Q

What is the striatum made of?

A

Caudate and putamen

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2
Q

What is the function of the substantia nigra (compacta)

A

Provides dopamine for basal ganglia pathway

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3
Q

NB: REVISE PATHWAY

A
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4
Q

What does the indirect basal ganglia pathway do?

A

Inhibits the thalamus

Less info back to cortex

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5
Q

What does the direct pathway of the basal ganglia do?

A

Stimulates thalamus

Go Pathway

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6
Q

List the functions of the basal ganglia.

A

Motor Function
- Helps motor cortex select appropriate motor cortex neurons for voluntary movement - initiation, scaling, sequencing
- Abnormal functioning = Parkinson’s/Huntington’s Disease
Cognitive/Psychological Functions
- Helps prefrontal cortex organize thoughts
- Helps limbic system organize emotions
- Reward-mediated learning, attention
- Abnormal functioning - drug addiction, ADHD, psychosis , Parkinson’s disease, Huntington’s disease
Dopamine in Basal Ganglia = Learning and Attention - reinforcement of preceding actions that produced reward (drug addiction, ADHD)

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7
Q

Describe the signs of Parkinson’s disease

A

· Signs: (Extrapyramidal)
- Resting tremor (pill rolling), 4-6 Hz
- Rigidity: lead-pipe (tone increases through range of motion), or with tremor “cogwheel”, not velocity dependent
- Akinesia, bradykinesia: lack of movement, slow movement, mask-like face, quiet speech, micrographia
- Posture and gait abnormalities: forward leaning posture, postural instability, retropulsion, shuffling gait, falls
- Dementia
- Depression
Autonomic dysfunction

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8
Q

When is the onset of parkinson’s disease?

A

45 - 70 years

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9
Q

What is the pathology behind PD?

A
· Death of dopamine neurons 
	- Idiopathic (80% of cases) - environmental factors, genetic predisposition
	- Genetic (single gene)
	- Specific toxin
Trauma
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10
Q

Why does loss of DA cause movement problems?

A

· Generation of movement requires selection of motor cortex neurons
· Basal ganglia usually select these neurons
· DA is needed to allow some pathways in basal ganglia to be selected instead of others
· Lack of DA = all pathways are equal
· Co-activation of agonists and antagonists = rigidity
Difficulty getting main agonists active enough to trigger movement

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11
Q

What is the treatment options for PD?

A

· Replace dopamine (L-dopa)
· Direct dopamine-receptor antagonists
· Surgical: stimulate basal ganglia nuclei (Deep Brain Stimulation)
Dopamine cell replacement - experimental

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12
Q

What causes Huntington’s disease?

A

Progressive death of medium spiny neurons in caudate/putamen

Unbalanced activity of surviving neurons

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13
Q

What is the inheritance of Huntington’s disease?

A

Autosomal dominant - repeated CAG triplets in Huntingtin gene

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14
Q

List the symptoms/signs of Huntington’s Disease

A

Motor Cortex Deficit - chorea (excessive, spontaneous, irregular, random, brief, abrupt movements), eventual loss of voluntary movement
Other cortex - dementia, mania, irritability, agitation, paranoia

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15
Q

What are the treatment options for Huntington’s disease?

A

There are none.

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16
Q

Name the different subregions of the cerebellum and their functions:

A

Spinocerebellum: posture, balance, locomotion (clinic: trunk ataxia, broad-based gait)
Cerebrocerebellum: planning and feedback to control limbs (clinic: hypotonia, intention tremor, limb ataxia)
Vestibulocerebellum: posture, eye movement (clinic: falls, vertigo, disordered eye movement)

17
Q

Name the two fibres bringing input into the cerebellum.

A

Climbing fibre input (intended movement)

Mossy fibre input (actual movement)

18
Q

What is the function of the cerebellum in motor control?

A

Helps to plan movement
Online correction
Motor learning
Perhaps helpful in cognitive functions

19
Q

What disorders would affect the cerebellum?

A

Stroke, alcoholic cerebellar degeneration, tumours, genetic, infection

20
Q

What are the signs of cerebellar disorder?

A
DANISH 
- Dysmetria 
- Ataxia 
- Nystagmus 
- Intention tremor
- Slurred speech 
- Hypotonia 
\+ Titubation
21
Q

What are the treatments for cerebellar disorders?

A
Treat causes (e.g. vitamin deficiency)
Symptomatic treatment, physiotherapy
22
Q

What are the clinical signs of a damaged spinocerebellum?

A

Trunk ataxia, broad-based gait

23
Q

What are the clinical signs of a damaged cerebrocerebellum?

A

Hypotonia, intention tremor, limb ataxia

24
Q

What are the clinical signs of a damaged vestibulocerebellum?

A

Falls, vertigo, disordered eye movement

25
Q

What is dysdiaochokinesia?

A

Decreased rapid alternating movements (part of ataxia which is a clinical sign of a damaged cerebellum)