ME03 - Motor System 2 - Cerebellum, Basal Ganglia Flashcards

(84 cards)

1
Q

Also called the little brain
Helps control the rate, range, force, and direction
of movements (SYNERGY)
o sequences motor activities
o monitors and makes corrective adjustments in motor activities while they are being executed silent area of the brain

A

Cerebellum

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2
Q

Electrical excitation does not cause any sensation. True or False?

A

TRUE

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3
Q

Damage does not produce paralysis. True or False?

A

TRUE

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4
Q

Where is Cerebellum located?

A

Located dorsal to the pons and medulla and protrudes from under the occipital lobes

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5
Q

3 Lobes of Cerebellum

A

ANTERIOR, POSTERIOR, FLOCCULONODULAR

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6
Q

Crosswise folds in the Cerebellar Cortex

A

Folia

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7
Q

Lie deep beneath the folded mass of cerebellar cortex

A

Deep Cerebellar Nuclei

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8
Q

Nuclei of Cerebellum from Medial to Lateral

A

DENTATE, EMBOLIFORM, GLOBOSE, FASTIGIAL

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9
Q

What are the Brainstem Attachments of Cerebellum

A

superior cerebellar peduncles to MIDBRAIN
middle cerebellar peduncles to PONS
inferior cerebellar peduncles to MEDULLA OBLONGATA

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10
Q

Contains a somatotopic map of the body surface

A

VERMIS and INTERMEDIATE ZONE
o Axial portions of the body lie in the vermis

o Limbs and facial regions lie in the intermediate zones

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11
Q

Lateral portions of cerebellar hemispheres do not have topographical representations. True or False?

A

TRUE

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12
Q

Function of the lateral portion of cerebellar hemisphere

A

o Receive input signals exclusively from cerebral cortex
o Plays important roles in planning and coordinating the body’s rapid sequential muscular activities

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13
Q

3 Layers of Cerebellar Cortex

A

Granular Layer | Purkinje Cell Layer | Molecular Layer

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14
Q

Innermost layer that contains granule cells, Golgi type II cells and glomeruli

A

Granular Layer

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15
Q

Middle layer that contains inhibitory Purkinje cells

A

Purkinje Cell Layer

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16
Q

Outermost layer that contains stellate and basket cells, dendrites of Purkinje and Golgi type II cells and parallel fibers (axons of granule cells)

A

Molecular Layer

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17
Q

2 Types of Fibers that are known as Excitatory Cerebellar Inputs

A

Climbing Fibers | Mossy Fibers

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18
Q

o Originate in the INFERIOR OLIVE
o Demonstrate complex spikes
_ Action potentials beginning with a strong spike and followed by a trail of weakening secondary spikes
o Function in conditioning Purkinje cells (motor learning)

A

CLIMBING FIBERS

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19
Q

o Form the bulk of the input, originating in the cortico-, vestibulo-, reticulo- and spinocerebellar tracts_o demonstrate SIMPLE SPIKES
Much weaker short-duration action potentials in Purkinje cells

A

MOSSY FIBERS

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20
Q

What are the Different Afferent Pathways to the Cerebellum

A

Pontocerebellar System | Olivocerebellar Projections | Spinocerebellar Fibers | Reticulocerebellar Fibers | Vestibular Fibers

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21
Q

o Largest afferent projections
o Originate from the basilar pontine nuclei

A

PONTOCEREBELLAR SYSTEM

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22
Q

Originate from the inferior olivary nuclei

A

OLIVOCEREBELLAR PROJECTIONS

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23
Q

Originate in spinal cord or medulla

A

SPINOCEREBELLAR FIBERS

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24
Q

Originate from brainstem

A

RETICULOCEREBELLAR FIBERS

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25
Originate from vestibular nuclei and vestibular apparatus
VESTIBULAR FIBERS
26
What are the Cells seen in Cerebellum
Purkinje cells | Granule cells | Golgi Type II Cells | Stellate Cells | Basket Cells | Glomerulus
27
o central neurons with fan-shaped dendritic trees o always inhibitory with GABA as its neurotransmitter
Purkinje cells
28
o smallest and most numerous neurons in the brain o parallel fibers are axons of granule cells o excitatory input from mossy fibers which use glutamate as its neurotransmitter
Granule cells
29
o small interneurons with numerous arborizations o inhibitory in function
Golgi Type II Celks
30
o inhibitory star-shaped cells found in superficial cerebellum
Stellate Cell
31
o inhibitory cells whose axons form baskets around Purkinje fibers and are found in deep cerebellar layers
Basket Cells
32
o complex of synapses having a mossy fiber at its core o synapsing with axons of Golgi type II neurons and dendrites of granule cells
Glomerulus
33
Modulates Purkinje cell output
Cerebellar Interneurons
34
All of the cerebellar interneurons are inhibitory EXCEPT _______________
Granule Cells
35
Have excitatory input to basket cells, stellate cells, Golgi II cells, and Purkinje cells
Granule Cells
36
Inhibits Purkinje cells (via parallel fibers)
Basket cells and Stellate cells
37
Inhibit granule cells, thereby reducing their excitatory effect on Purkinje cells
Golgi II cells
38
Only output of the cerebellar cortex
Purkinje Cells
39
Output is always inhibitory, using _______________ as NT
GABA
40
Inhibitory output modulates the output of the cerebellum and regulates rate, range, and direction of movement (synergy). True or False
TRUE
41
Projects to fastigial nucleus, vestibular nucleus and reticular formation
Vermis
42
Project to globose and emboliform nuclei (interposed nuclei)
Intermediate Zone
43
Project to the dentate nucleus, ventral anterior thalamic nuclei and cerebral cortex
Lateral Hemispheres
44
Follow the Cerebellar Pathway
Cortex >> Pons* >> Cerebellum >> Dentate nucleus* >> Red Nucleus >> Thalamus >> Corticospinal tract
45
o consists of the small flocculonodular lobes o for control of balance and eye movement
Vestibulocerebellum
46
Consists of lateral zones of cerebellar hemispheres For planning and initiation of movement
Cerebrocerebellum
47
o consists of vermis and intermediate zones o for control of rate, force, range, and direction of movement (synergy)
Spinocerebellum
48
o During nearly every movement, certain muscles must be rapidly turned on and then quick turned off
TURN ON/TURN OFF FUNCTION
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TURN ON/TURN OFF FUNCTION is made possible by
Made possible by interplay of mossy and climbing fibers and Purkinje cells
50
What fibers are involved in Motor Learning?
CLIMBING FIBERS. Climbing fibers modify sensitivity to parallel fiber input o when mismatch between anticipated result of movement and its actual result occurs, climbing fiber input is more vigorous o as movement is practiced, mismatch declines gradually
51
o During any movement, momentum develops and must be overcome to stop the movement o Appropriate learned, subconscious signals from spinocerebellum stop the movement precisely at the intended point
Damping Function
52
Patient with cerebellar lesion assumes unsteady stance and reeling gait (like a drunk person)
Ataxia
53
How does a Patient with Ataxia compensate?
To compensate, he assumes a broad-based stance and a broad-based gait
54
Failure to meter the contractions that set the distance of motion
Dysmetria
55
Inability to perform rapid alternating movements
Dysdiadochokinesia
56
Failure of a movement to be terminated at a proper time
Past Pointing
57
Difficulty in maintaining position against sudden unexpected displacement
Overshooting
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Slowness and slurring of speech
Dysarthria
59
Volume of voice varies from low to high from peak to peak
Scanning Speech
60
Tremor of intentionally maintained head or trunk posture or of a limb suspended in front of the body
POSTURAL, POSITIONAL or STATIC TREMOR
61
Unsteady oscillations of the head or trunk
TIUTIBATION
62
o Tremor as a limb approaches its target o Results from cerebellar overshooting and failure of the cerebellar system to "damp" the motor movements
INTENTION, END-POINT or KINETIC TREMOR
63
Jerkiness of eye movement o rapid, tremulous movements of the eyes rather than steady fixation
Nystagmus
64
What is affected in Nystagmus?
Nystagmus is due to failure of damping by the cerebellum Occurs especially when the flocculonodular lobes of the cerebellum are damaged
65
Decreased tone of the peripheral body musculature on the side of the cerebellar lesion
Hypotonia
66
What is affected in Hypotonia?
Results from loss of cerebellar facilitation of the motor cortex and brain stem motor nuclei
67
Extremity tested swings to and fro several times like a pendulum after eliciting the reflex seen in HYPOTONIA
Pendulous reflexes
68
What are the Different Cerebellar Syndromes
ANTERIOR (ROSTRAL) VERMIS SYNDROME_- involves the anterior cerebellar lobe ; o ataxia of the lower limbs only POSTERIOR (CAUDAL) VERMIS SYNDROME - involves the flocculonodular and posterior lobes ; o axial ataxia without extremity ataxia CEREBELLAR HEMISPHERE SYNDROME - cerebellar signs lateralized to one half of the body PANCEREBELLAR SYNDROME_- bilateral cerebellar signs due to involvement of all cerebellar lobes
69
Deep cerebral nuclei involved in motor control modulates thalamic outflow to the motor cortex to plan and execute smooth movements demonstrates programming functions o generate basic patterns of movement in response to cues from cortical association areas
Basal Ganglia
70
Components of Basal Ganglia
Globus Pallidus | Putamen | Caudate Nucleus | Subthalamic Nucleus of Substantia Nigra Globus Pallidus x Putamen = Lentiform Nucleus Putamen x Caudate Nucleus = Striatum Lentiform Nucleus + Striatum = Corpus Striatum CORPUS STRIATUM + SUBTHALAMIC NUCLEUS OF SUBSTANTIA NIGRA = BASAL GANGLIA
71
NT used in connections between striatum and substantia nigra
Dopamine
72
Dopamine in relation to Basal Ganglia Pathways
o inhibitory on the indirect pathway (D2 receptors) o excitatory on the direct pathway (D1 receptors) o overall action is excitatory
73
Responsible for the COGNITIVE CONTROL OF MOTOR ACTIVITY o most of our motor actions occur as a consequence of thoughts generated in the mind
CAUDATE NUCLEUS
74
Controls the speed and size of movement
Basal Ganglia
75
Locus for Spatial Coordination
Posterior Parietal Cortex
76
TIMING AND SCALING FUNCTIONS are lost with lesions in the?
Basal Ganglia, specifically CAUDATE NUCLEUS
77
snake-like or writhing movements of the hand and arm or face result from lesions of the GLOBUS PALLIDUS
Athetosis
78
flailing movements of the extremities result from lesions to the SUBTHALAMIC NUCLEUS OF LUS
Hemiballismus
79
brief, irregular, non-purposeful movements that are vaguely comparable to dancing result from lesions to the CORPUS STRIATUM (specially on caudate nucleus)
Chorea
80
Results from widespread destruction of the dopaminergic cells in the substantia nigra
Parkinson's Disease
81
Manifestations of Parkinson's Disease
o cogwheel rigidity o resting pill-rolling tremor o slowness or difficulty in initiating movement (bradykinesia, akinesia) o postural instability (shuffling or FESTINATING gait)
82
Autosomal dominant genetic disorder caused by CAG trinucleotide repeats o displays ANTICIPATION with succeeding generations
Huntington's Disease
83
Characteristics of Huntington's Disease
Characterized by flicking movements in individual muscles (chorea) o leads to progressive severe distortional movements
84
Huntington's Disease is caused by the depletion of what neurotransmitters?
Depletion of GABA and acetylcholine from many areas of the brain