Corticobulbospinal Tracts & Basal Ganglia Motor Systems II Flashcards

1
Q

baseline activity

A

can increase or decrease

-change in frequency of APs

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2
Q

disinhibition

A

removal of inhibitory effect of stimulus

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3
Q

basal nuclei

A

subcortical grey matter

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4
Q

components of basal nuclei

A
striatum (caudate + putamen)
globus pallidus (external and internal)
nucleus accumbens
subthalamic nucleus
substantia nigra
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5
Q

lentiform nucleus

A

putamen and globus pallidus

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6
Q

GPe and GPi

A

globus pallidus internal and external

internal - medial
external - lateral

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7
Q

division of substantia nigra

A

pars compacta - dopamine
-lost in parkinsons Dx
pars reticulata

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8
Q

basal nuclei arrangement

A

paired parallel circuits

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9
Q

role of basal nuclei

A

determine what behavior is appropriate

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10
Q

direct pathway

A

yes pathway

-basal nuclei > cortex

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11
Q

indirect pathway

A

no pathway

-basal nuclei > cortex

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12
Q

basal nuclei

A

balance of direct vs. indirect pathway

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13
Q

3 kinds of behavior through basal nuclei

A

motor
cognition
affect (emotion)

not vision / audition**

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14
Q

seen rostrally

A

nucleus accumbens

appears to connect caudate and putamen

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15
Q

input to basal nuclei

A

striatum

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16
Q

output of basal nuclei

A

GPi and SNr

influence cortex via thalamus

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17
Q

to striatum

A

motor activity
cognitive processes - prefrontal
emotional behavior - limbic

18
Q

caudate

A

cognitive processes

19
Q

ventral striatum

A

emotional behaviors

20
Q

putamen

A

motor activity

21
Q

basal nuclei blood supply

A

branches of anterior cerebral artery - caudate head and nucleus accumbens

branches of middle cerebral artery (lenticulostriate ) - lentiform and striatum

branches of posterior cerebral artery - substantia nigra and subthalamic nucleus

22
Q

basal nuclei pathology

A

movement disorders
-don’t affect strength, coordination, or sensation

affect voluntary systems**

23
Q

akinetic

A

without movement

24
Q

negative sign

A

reduced movement

25
Q

positive sign

A

increased movement

26
Q

hypokinesia

A

reduced movement

27
Q

bradykinesai

A

slow movement

28
Q

dyskinesia

A

inappropriate movements

29
Q

tremor

A

oscillatory movement

-at rest, decreased with voluntary movement

30
Q

athetosis

A

slow, writhing movement

31
Q

chorea

A

abrupt, rapid, jerking, dance-like movements

32
Q

choreoathetosis

A

overlap of athetosis and chorea

33
Q

ballism

A

violent jerking of one limb

usually unilateral - hemiballismus

34
Q

parkinsons

A

cause unknown
degeneration of SNc

lack in melanin containing dopaminergic neurons

35
Q

Sx of parkinsons

A

hypokinesia and bradykinesia

  • negative signs
  • gait - small shuffle steps
  • facial masking - no facial communication
  • tremor and rigidity
  • positive signs

loss of postural reflexes
-close eyes, shove, can’t recover

36
Q

substantia nigra compacta

A

drives cortex

  • increase direct loop
  • decrease indirect loop
37
Q

parkinsons therapy

A

L-dopa
-doesn’t work long term

replace missing cells
-will get killed too

deep brain stimulation

38
Q

huntingtons disease

A

earlier onset - age 30-40
multiple CAG repeats on chromosome for protein huntungtin
-results in cell death

autosomal dominant

39
Q

pathology of huntingtons

A

degeneration of striatum

-loss of cholinergic neurons

40
Q

Sx of huntingtons

A

hyperkinesias
-choreoathetosis

dementia and cognitive changes

little treatment

hallucinations/paranoia