Caudate Nucleus Strength of Movement
Transcript of Caudate Nucleus Strength of Movement
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Neuro tutoring
Block 7 Week 2
1. How are the cells of the cerebellum organized into layers?
Pia
Molecular- purkinje dendrites, basket, stellate cells
**Purkinje- purkinje cell bodies
Granular- granule cells, golgi cells
White
2. What are the 5 cell types of the cerebellum and their functions, connections, and neurotransmitters?
Purkinje (large): GABA (-) (inhibitory) to deep cerebellar nuclei. Dendrite tree radiates perpendicular to
folia.
Granule: Glu (only excitatory) smallest, one axon can excite many purkinje fibers, parallel to folia axis.
Golgi: GABA (-) to granule cells. Interneurons.
Basket: GABA potent (-) of purkinje Stellate: GABA (-) of purkinje
Spinal Cord/Cortex/red nucleus/cerebellum contralateral Inf. Olivary nuc (ION) climbing fibers (+)
purkinje (-) deep nuclei output
Moss fibers (+) granule cells (+) parallel fibers purkinje
Golgi (-) granule cells
Basket and stellate cells
(-)
purkinje
3. What are the functions and pathways associated with the following structures?
-flocculonodular lobe: eye movement (VOR) and balance
vestibulocerbellum: vestibular input from mossy fibers
-vermis:postural adjustments
spinocerebellum: get input from mechanoreceptors (trunk and neck). Controls axial/trunk and proximal
limb movement.
-intermediate zone: input from neck, trunk, limbs
spinocerebellum: distal limb movement
-lateral zone: movement planning and initiation and learning
cerebrocerebellum: major input from cortex and pons
-inferior cerebellar peduncle: restiform body
afferents from spinal cord and brainstem (spinocerebellar)
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-middle cerebellar peduncle: branchium pontis; largest; cerbrocerebellar afferents; cortex pons
cerebrocerebellum
-superior cerebellar peduncle:brachium conjuntivum; mainly efferents from deep nuclei to thalamus, red
nuclei, descending tracts
4. How would you describe the locations and functions of the 4 deep cerebellar nuclei?
Dentate: largest, most lateral
Emboli form/Globose: interposed nuclei
Fastigial: most medial; more vermal inputs
**All outputs are excitatory except to ION (GABA)
5. What are the main functions of the cerebellum and its associated tracts?
Function: modulates descending tracts: movement and posture, motor learning compares intention with actual
movement, and compensates for errors
-lateral zone:
-intermediate zone:
-vermis:
-flocculonodular lobe:
-corticopntocerebellar: movement planning
-ventral spinocerebellar: monitoring descending and peripheral information regarding movement
-dorsal spinocerebellar: cerebellum gets feedback from periphery during movement
-dentarubrospinothalamic: adjusts motor output
6. What are the 2 types of afferent fibers to the cerebellum?
1) climbing fibers:
o Innervate purkinje (1 climbing fiber per purkinje)
o Form contralateral ION (+) purkinje dendrites in molecular layer
o Complex spike: 1-3 spikes/sec (know what it looks like) may also modulate mossy fiber input 2) Mossy fiber:
o Excite granule cells (2 purkinje)
o Will excite multiple dendrites
o Simple spike- up to 200/sec
7. Describe the main afferent and efferent pathways of the cerebellum:
5 afferents
o 1) Vestibulonuclei juxtarestiform body vestibulocerebellum (floculonodular body)
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Reciprocal connections control eye movements and body equilibrium while standing ormoving
o 2) Ipsilateral spinal cord/lower medulla/contralateral ION (Dorsal) restiform body
spinocerebellum (vermis and int.)
o 3) Contralateral spinal cord (ventral) superior cerebellar peduncle contralateral
spinocerebellum (vermis and int. zone)
cross twice end up ipsilateral
o 4) Contralateral cortex pontine nuclei middle peduncle (brachium pontis)
cerebrocerebellum (lateral)
o 5) Monoaminergic fibers: from brainstem
raphe nuclei 5HT (serotonin)
locus cerelus NE (noradrenergic)
4 Major Efferents: all exit via superior cerebellar peduncle
o 1) flocculonodular vestibular nuclei
o 2) vermis: ongoing movement control
Vermis (-) fastigial nuclei (+) brainstem medial descending tracts
proximal limb and axial
Vermis (-) fastigial nuclei (+) motor nuclei of thalamus motor andpremotor cortex
o 3) Int. Zone: ongoing movement control of distal limbs
Interposed nuclei red nuclei lateral descending tracts distal limb
Interposed nuclei
thalamus
motor and premotor cortex
corticospinal tract
distal limb
o 4) Lateral Zone: Initiation, planning, timing of voluntary movements
Crosses 2 times so you get ipsilateral loss with lesion
Dentorubrspinothalamic tract:
Dentate corticopontine tract lateral zone
Dentate corticospinal tract spinal cord
Dentate red nucleus thalamus motor/premotor cortex
8. Symptoms of cerebellar dysfunction:
1) appendicular ataxia: agonist and antagonist arent coordinated; ipsilateral
2) dysdiadechkinesia: difficulty with rapid alternating movements; ipsilateral
3) Titubation: cant maintain upright posture (trunk muscles); lesion to vermis/floculonodular
4) Gait Imbalance: leg ataxia and impaired VOR suppression
5) Impaired VOR suppression: eyes following moving objects will be jerky; vermis isnt allowing
proper VOR suppression
6) Scanning Dysanthmia: clipped words; hesitation between syllables
7) decreased muscle tone, decreased reflexes: because cerebellar input via deep nuclei is primarily
excitatory
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9. What are some potential causes of cerebellar disorders?
Ischemic stroke/hemorrhagic stroke
Tumor
Infection
Atrophy: etOH, affects legs >>> arms (medial cerebellum)
10. What are the components of the basal ganglia?
Striatum: GABA
o
Caudate nucleus: cognitive function, less motor involvemento Putamen: motor function
Globus Pallidus: GABA
o GPe, GPi
STN (Subthalamic Nucleus): Glu
Substantia Nigra
o SNc- pars compacta: dorsal and dopaminergic (DA)
o SNr- pars reticulata: ventral (GABA)
Nucleus acumbens: connects caudate to putamen (DA)
GPi and SNr are final output of basal ganglia
Corpus striatum: putamen, caudate, GP Lentiform
11. Describe the direct and indirect pathways of the basal ganglia:
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12. What are the general functions of the basal ganglia? Regulate movement
Influence descending motor tracts
Control eye movements
Memory orientation in space
Contributes to cognition (caudate)MD and prefrontal cortex
Limbic function
Final Test Question: All of the following control eye movement except....
13. What are some symptoms of basal ganglia dysfunction? NT problem
Abnormal motor/movements: releasing motor cortex from inhibition
Resting tremor: pill rolling (Parkinsons)
Athetosis: striated lesion
Hemiballismus: STN lesion; contralateral
Dystonia: abnormal posture
Bradykinesia: slow movements
14. Describe the lesion and its associated symptoms in the following basal ganglia disorders:
-Huntington disease
Bilateral atrophy of caudate due to increased CAG repeats on chromosome 4
Autosomal dominant
Hyperkinesias from lesion to indirect pathway
Chorea, athetosis (excess movement)
Memory loss, cognitive dysfunction, psych disturbance
-Parkinsons disease
Direct pathway lesion: lose DA neurons at SNc
Bradykinesia
Hypophonic voice
Mask-like facial expression
Tardive dyskinesia: from L-Dopa treatment; involuntary face and tongue movement
-hemiballismus
Indirect path lesion; excess movement
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-stereotactic surgery
1) Pallidotomy: lesion of GPi in indirect pathway, trying to induce hyperkinesias to correct for
bradykinesia and rigidity
o Most dramatic effect; contralateral
2) Thalamatomy: lesion thalamus in direct pathway, stops movement induction; use: treat severe tremor
3) Deep brain stimulation: inhibit STN with high frequency stimulation; use to treat bradykinesia and
rigidity (inhibit indirect pathway)o Has contralateral effects
15.
Cerebellum Basal Ganglia
Input from spinal cord
Direct
None (input is cortical and
thalamic)
Output to spinal cord No direct output No direct output
Connections with brainstem Brainstem connections Less: SNc/SNr
Cortical connections Indirect via pons Direct cortical
Thalamic projections Yes Yes
Output Excitatory Inhibitory (through indirect)Disinhibitory (through direct)
*via thalamus
Function Coordinate movement execution;compare intention with actual
Planning and execution of complexmotor strategies; amplitude,
velocity, and strength of movement
Lesions Ipsilateral symptoms Contralateral of bilateral symptoms
Symptoms of lesions Intentional tremor, ataxia, impaired
balance
Resting tremor, hypokinesia
(Parkinsons)/hyperkinesias
(Huntingtons)