Chapter 5 Flashcards

1
Q

basal ganglia located all over the brain but all have one thing in common

A
  • prepare the starting and stopping of voluntary motions, by means of direct and indirect pathways for motor movements
  • work together
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2
Q

major components of basal ganglia

A
  • caudate and putamen (striatum)
  • globus pallidus
  • subthalamic nucleus
  • substantia nigra
  • nucleus accumbens
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3
Q

basal ganglia striatum

A

caudate nucleus and putamen

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4
Q

direct pathways for motor movements in the basal ganglia

A

implicated in functions concerned with the initiation (or excitation) of motor movements

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5
Q

indirect pathways for motor movements in the basal ganglia

A

implicated in the stopping (or inhibition) of motor movements

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6
Q

movement disorders (basal ganglia disorders) classified into two broad categories

A

hyperkinetic disorders and hypokinetic disorders

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7
Q

hyperkinetic disorders

A

when the excitatory pathways become overactive relative to the inhibitory pathways

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8
Q

hypokinetic disorders

A

when the inhibitory pathways become overactive relative to the excitatory pathways

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9
Q

substantia nigra divided into two parts

A

pars compacta (SNc) and pars reticulata (SNr)

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10
Q

pars compacta (SNc) of the substantia nigra

A

source to one of the major domaince projections, the nigrostriatal pathway (from SNc to neostriatum)

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11
Q

pars reticulata (SNr) of the substantia nigra

A

mostly GABA (inhibitory) neurons to thalamus

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12
Q

dopamine

A

excitatory

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13
Q

GABA

A

inhibitory

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14
Q

Parkinson’s Disease

A
  • movement disorder
  • results from the degeneration of the pars compacta neurons
  • characterized by: muscle rigidity, bradykinesia/akinesia, resting tremor
  • most common treatment is replacement therapy with L-DOPA, a precursor of dopamine
  • can treat by lesioning part of the pars compacta (SNc) to reduce inhibition of dopamine
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15
Q

hypokinetic disorder

A

Parkinson’s disease

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16
Q

stages of progression of physical signs of Parkinson’s disease

A
  • stage 1: unilateral movement; early masking of facial expression, affected arm in semiflexed position with tremor
  • stage 2: bilateral involvement with early postural changes; slow, shuffling gait with decreased excursion of legs
  • stage 3: pronounced gait disturbances and moderate generalized disability; postural instability with tendency to fall
17
Q

hyperkinetic disorders

A
  • Huntington’s disease
  • Hemiballismus
  • Athetosis
18
Q

nigrostriatal pathway

A

from the substantia nigra in the midbrain, dopamine, to the caudate/putamen (straitum)
- initiate movement

19
Q

reverse of nigrostriatal pathway

A

from the caudate/putamen (striatum), GABA, to the substantia nigra
- stop movement

20
Q

Huntington’s Chorea

A

symptoms include:
- involuntary jerking or fidgety movements of the limbs and body
- stumbling and clumsiness
- cognitive impairment: difficulty planning and determining the direction of movement
- emotional and motivational issues: difficulty controlling the emotional and motivational aspects of movement

  • no caudate, so no GABA –> over-movement
21
Q

Hemiballismus

A
  • onset can occur at any age and always due to stroke
  • damage in subthalamic nucleus (STN) or globus pallidus (GPc)
  • severe contralateral flinging movements (arms or legs)