4.2 Basal ganglia and cerebellum Flashcards

1
Q

The pyramidal system (main output to voluntary muscles) occurs via the ______________, and the output is modulated by the extrapyramidal system (basal ganglia & cerebellum):
• Impinge on the motor cortex to refine the outputs of the cortex on the way down to the motor neurones in the spinal cord
• Basal ganglia has an _____________ via the thalamus, while cerebellum has a _____________- via the thalamus → balance allows for smooth coordinated movement
• Disturbances in either system will present as movement disorders

A

corticospinal tract;

inhibitory effect;

positive effect

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2
Q

What does the basal ganglia consist of?

A

grey matter areas within the subcortical part of the brain:
1. Caudate nucleus and putamen
2. Internal and external globus pallidus (GPi and GPe)
3. Subthalamic nucleus (STN) 4
. Pars reticulate & pars compacta of substantia nigra (SNr and SNc)
*Lentiform nucleus is made of the putamen and globus pallidus, while the striatum is made of the caudate nucleus and lentiform nucleus.

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3
Q

From the cerebral cortex, the ____________________ (5) all project to the caudate nucleus and putamen:
• Putamen then projects via the direct pathway (to ___________) or the indirect pathway (to the _____________i)
o Refer to “Drugs Affecting the CNS – Parkinson’s disease” for more details
• _____________ are the only output of the basal ganglia, and project to the thalamus
• Thalamus then projects back to the ________________ → involved in movement preparation and planning

A

supplementary motor area (SMA), premotor area (PMA), primary motor cortex (M1), somatosensory cortex, and parietal cortex;

GPi and SNr;

GPe → STN → GP;

GPi and SNr;

cortex (SMA and PMA)

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4
Q

The globus pallidus (GPi) inhibits the __________ and the ____________ inhibits the GPi (via GABA), which thus releases the thalamus from inhibition:
• Thalamus releases selected movement via _________________
• Correct balance is mediated by the SNc (provides excitatory inputs to the _______________ (via dopamine)) → nigro-striatal pathway (positive excitatory)
• GPi and SNr are the messengers of all information from the basal ganglia (inhibits the thalamus)

A

thalamus;

putamen;

projections to cortex (positive innervation);

caudate nucleus and putamen

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5
Q

[Parkinson’s disease]
The substantia nigra is pigmented by _____________ (by-product of normal metabolism in dopaminergic neurones) → gets darker with age due to build-up:
• Parkinson’s disease occurs due to __________________ (nigro-striatal pathway) → indicated by pallor of substantia nigra
• Positron Emission Tomography (PET) 18F-DOPA (visualising dopaminergic innervation in the caudate nucleus and putamen): symmetrical in normal subjects; __________________ in Parkinson’s patients
o Unilateral in onset, then progresses to bilateral loss

A

neuromelanin ;

neuronal degeneration of the substantia nigra;

asymmetry and loss of dopamine signal in the basal ganglia;

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6
Q

Patients with Parkinson’s disease present with the following signs and symptoms due to _______________ (impaired nigro-striatal excitatory pathway → no release)

  • bradykinesia: Slowness of movements (slow walking, small steps, shuffling feet, reduced arm swing, ______ turning)
  • difficulty in small movements e.g. buttoning of shirt
  • face _________: Absence of movements which normally animate the face → expressionless and mask-like face
  • _______: Difficulty initiating movements → require external sensory triggers to initiate movement (e.g. visual trigger; internal initiation impossible)
  • Tremor at rest: Cease with ________, usually starts in one hand (asymmetry) and tends to spread with time to other parts of the body
  • Rigidity (not spasticity): Type of resistance to passive movements → passively moving the patient’s limb feels like _______________
  • ___________ posture: Head and body bent forward and downwards
A

increased inhibition from GPi

en-bloc;

voluntary activity;

hypomimic;

akinesia

bending a lead pipe (lead pipe rigidity);

Stooped

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7
Q

Huntington’s disease is caused by an autosomal dominant mutation in the _________________(CAG repeat disease):
• Due to degeneration of spiny GABAergic neurones in the striatum (____________ first then ______________ later) → may produce profound atrophy of both
• Present with _______________ → rapid jerky involuntary movements of the body (usually affecting hands and face at first) → no inhibition of thalamus
o Patients can mask the spontaneous movements (early stages) by incorporating them into socially acceptable movements o Gradually increase over time until the patients become totally incapacitated ]
• Eventually experiences cognitive decline and dementia, with death occurring 10 – 15 years after the onset of symptoms

A

huntingtin gene on chromosome 4 ;

caudate nucleus ;

putamen;

choreic movements (chorea)

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8
Q

The cerebellum makes up the roof of 4th ventricle and lies immediately posterior to the pons:
• Cerebellum and brainstem occupy the posterior cranial fossa with the occipital lobe superior to it (separated by the _____________)
• Can be divided horizontally into 3 lobes (_______, ________, _______) or sagittally into 3 lobes (________ in midline, ___________, and _______ cerebellum

A

tentorium cerebelli;

anterior, posterior, flocculonodular;

vermis; intermediate; lateral

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9
Q

what does the deep nuclei (in white matter of cerebellum) contain?

A

Deep white matter contains distinct nuclei (neuronal cell bodies):
• Dentate nucleus is the largest, and is the main output nucleus
• Other nuclei include the interposed nucleus and fastigial nucleus

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10
Q

What is the structural functions of the cerebellar peduncles?

A

fibre tracts with both functional and structural roles → holds cerebellum to the back of the brainstem at the level of the pons

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11
Q

what does the superior cerebellar peduncle contain?

A

Main output pathway (in terms of modulating motor function)

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12
Q

what does the middle cerebellar peduncle contain?

A

Largest; bridging fibres joining the 2 halves of the cerebellum

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13
Q

what does the inferior cerebellar peduncle contain?

A

Consists of ascending fibres from the spinal cord

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14
Q

The vestibulocerebellum includes the ____________ lobe (oldest part of the cerebellum):
• Receives input from the vestibular system (__________________) to the flocculonodular cortex (reciprocal connections through the _____________)
• Involved in the regulation of _______________and coordination of head movements with eye movements (e.g. watching
tennis)

A

flocculonodular ;

vestibular nuclei of CN VIII and the vestibular nerve;

inferior cerebellar peduncle;

gait, posture, and equilibrium

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15
Q

The spinocerebellum consists of the vermis (projects to the ____________) and the intermediate cerebellum (projects to the ______________):

• Input from spinal cord (dorsal & ventral spinocerebellar tracts):
o Vermis: from _________________
o Intermediate cerebellum: from the __________
o Cerebellar cortex is organised somatotopically

  • Output occurs via the __________ (via fastigial and interposed nuclei) → _________ (midbrain) → ____________ (pons) → ________________ tracts → spinal cord motor neurones
  • Modulates voluntary movement based on proprioception input through cerebellum → coordination of speech and limb movements and adjustment of muscle tone
A

fastigial nucleus;

interposed nucleus;

axial parts of the body, trigeminal, visual, auditory inputs ;

limbs;

superior cerebellar peduncle;

red nucleus;

reticular formation nuclei;

reticulospinal and rubrospinal

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16
Q

The cerebrocerebellum includes the _________(projects to the ______________):
• Receives input from the _______________ nuclei (via middle cerebellar peduncle) and the _______________i (via inferior cerebellar peduncle)
• Some connectivity exists within the cerebellum
• Outputs from the dentate nucleus (via the superior cerebellar peduncle) → __________ → cortical projections to main
motor cortical areas → project back down to the _________________
• Involved in coordination of ______________

A

dentate nuclei;

lateral lobes;

reticular formation and pontine;

inferior olivary nucle;

thalamus;

reticular formation, pontine nuclei and inferior olivary nuclei;

skilled movements (e.g. playing the piano) and tactics of immediate movements

17
Q

what is the definition of ataxia (sign of cerebellar disorder)?

A

Instability when standing or walking, wide-based stance, staggering and wide-based walking (looks drunk):
• Muscles involved differ d

18
Q

what is the negative romberg sign (sign of cerebellar disorder)?

A

Loss of balance even when patient opens his eyes while standing

19
Q

What is hypotonia (sign of cerebellar disorder)?

A

Reduced muscle tone (floppy limbs)

20
Q

What is dysmetria (sign of cerebellar disorder)?

A

Inability to judge distance and when to stop (cannot control range of movement)

21
Q

What is dysarthria (sign of cerebellar disorder)?

A

Slurred speech (cannot articulate words correctly) and inappropriate phrasing

22
Q

What is dysdiadochokinesia (sign of cerebellar disorder)?

A

Inability to coordinate movements (cannot perform rapidly-alternating movements) → heel-to-shin/finger-to-toe test

23
Q

what is intention tremor (sign of cerebellar disorder)?

A

when limb approaches target

24
Q

What is nystagmus (sign of cerebellar disorder)?

A

Involuntary rapid eyeball oscillation (horizontal/vertical/rotary) with the fast component towards the side of lesion

25
Q

what is postural tremor (sign of cerebellar disorder)?

A

when fixed posture/weight bearing is attempted

26
Q

what is scanning speech (sign of cerebellar disorder)?

A

Slow enunciation with tendency to hesitate at beginning of a word/syllable

27
Q

what are the more prominent signs of vestibulocerebellum disorder?

A

Loss of balance while standing upright, eye movement abnormalities (e.g. nystagmus), hypotonia

28
Q

what are the more prominent signs of spinocerebellum disorder?

A

Truncal ataxia (wide-based gait with small shuffling movements), dysdiadochokinesia, dysmetria, speech disorders (e.g. dysarthria or staccato speech), action/intention tremors

29
Q

what are the more prominent signs of cerebrocerebellum disorder?

A

Impairments in highly skilled sequences of learned movements (e.g. playing musical instrument)