Lecture 11: Motor Systems Flashcards

1
Q

Distinguish between direct and indirect corticobulbar fiber

A

Direct: fibers that project to cranial motor neurons

Indirect: fibers that project to midbrain and pontine reticular formations adjacent to CN nuclei

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2
Q

Where are axons terminating in upper spinal cord levels vs. lower spinal cord levels located in the posterior limb of the internal capsule?

A
  • Axons terminating in upper spinal cord levels are rostral
  • Axons terminating in lower levels are caudal
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3
Q

The Supplementary Motor Cortex is in which Brodmann’s area and is involved in what function?

A
  • Medial portion of Area 6
  • Involved in organizing or planning the sequence of muscle activation required to make a movement
  • M1 will be the one executing the movement
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4
Q

The Premotor Cortex is located in what Broadmann’s area and is closely associated with what other cortex?

A
  • Area 6
  • Closely associated with Supplementary Cortex
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5
Q

Premotor cortex receives inputs from where and projects to which areas?

A
  • Receives inputs from sensory areas of the parietal lobe
  • Projects to M1, the SC, and RAS
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6
Q

The Premotor cortex is involved with what function of movement?

A
  • The PREPARATION to move
  • Organizes those postural adjustments required to produce movement
  • Directs control of proximal limb muscles use to position the arm for movement tasks or to orietn the body for movement
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7
Q

What artery may contribute to the catastrophic lesions of the posterior limb of the internal capsule and what deficits will occur?

A
  • Lenticulostriate branches of the M1 segment of the MCA
  • Motor symptoms in the contralateral UE and LE’s = weakness and transient flaccid paralysis
  • Followed by spastic paralysis (UMN signs) that typically never resolve
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8
Q

What makes up the striatum?

A

Caudate + Putamen + Nucleus Accumbens + Olfactory Tubercle

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9
Q

What 3 things make up the Corpus Striatum?

A

Globus pallidus + Caudate + Putamen

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10
Q

What 2 things make up the Lentricular nucleus?

A

Globus pallidus + Putamen

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11
Q

What 2 things make up the neostriatum?

A

Caudate + Putamen

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12
Q

What is the Subthalamic Fasciculus (Basal Nuclei Tract); what type of fibers?

A
  • Reciprocal fiber tracts between globus pallidus and subthalamus
  • Contain excitatory fibers
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13
Q

What are the Nigro-Thalamic Fibers (Basal Nuclei Tract); where do they terminate and is it the same area as the fibers from globus pallidus?

A
  • Non-dopaminergic fibers that originate in pars reticularis of substantia nigra
  • Terminate in VA and VL thalamic nuclei

*Fibers from the globus pallidus and the substantia nigra DO NOT terminate in the same areas of the VL and VA thalamic nuclei

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14
Q

What are the Nigro-striatal fibers (Basal Nuclei tracts); where do they terminate and what disease are they related to?

A
  • Dopaminergic fibers that originate in pars compacta of substantia nigra
  • Terminate in the caudate and putamen
  • Neurons in this area of the substantia nigra are destroyed in Parkinson’s disease
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15
Q

Neurons in which area are destroyed in Parkinson’s disease?

A

Dopaminergic fibers that originate in pars compacta of the Substantia Nigra

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16
Q

What are the Striatonigral fibers (Basal Nuclei tract); what disease are they related to?

A
  • GABAergic fibers (INHIBITORY) originate in putamen
  • Terminate in the pars compact of the substantia nigra and medial/lateral segments (GP)
  • Thought to contribute to Huntington’s disease
17
Q

Huntington’s disease is caused by loss of what type of neurons; typically recognized on imaging as atrophy where?

A
  • Loss of INHIBITORY GABAergic neurons of the basal ganglia (Striatonigral fibers)
  • Atrophy of the caudate nucleus with concomitant enlargement of the frontal horns of the lateral ventricles
18
Q

What is Syndenham’s Chorea (cause and presentation)?

A
  • Childhood autoimmune disease
  • Major manifestation of rheumatic fever (infection with group Aβ-hemolytic streptococci)
  • Present with rapid, irregular, aimless movements of the limbs, face, and trunk.
19
Q

What is Ballismus, how does it present, and what causes it?

A
  • Most typically presents as hemiballismus
  • Uncontrolled flinging (ballistic) movements of limb
  • Common with vascular lesions localized to contralateral SUBTHALAMIC NUCLEUS or SUBTHALAMIC FASCICULUS
20
Q

What is Chorea, how does it present, and what causes it?

A
  • Rapid, irregular, involuntary, dance-like movements that flow randomly from one body region to another
  • Characteristic of Huntington disease, but may occur as side effect of treatment in Parkinson disease
  • Loss of neurons in indirect pathway
21
Q

What is Athetosis, how does it present, and how is it classified when the movements are more brisk and when more intense?

A
  • Continous writhing of distal portions of one or more extremities
  • Slow, sinous, and writhing movements more obvious in the UE and hands/face
  • When more brisk and resemble chorea —> choreoathetosis
  • When more intense, sustained, and resemble dystonia —> athetotic dystonia
22
Q

Corticonuclear fibers consist of UMN’s that influence which nuclei of CN’s?

A
  • Motor nuclei of CN V, VII, XII
  • Nucleus Ambiguus of CN IX and X
  • Accessory nucleus of CN XI
23
Q

The nucleus accumbens and olfactory tubercle comprise what structure that links the amygdala and hippocampus to the dorsalmedial nucleus of the thalamus and the globus pallidus; what role does this nucleus have in movement?

A
  • Comprise the Ventral Striatum
  • Nucleus accumbens plays a role in the motivational and emotional aspects of movements
24
Q

What are the motor nuclei of the thalamus?

A

Ventral anterior and Ventral lateral nuclei