Chapter 15 Flashcards

(37 cards)

1
Q

Functions of BG

A

Refinement of cortically initiated motor activity

By suppression of competing movements extraneous to the target motor activity

Regulation of associated automatic motor movements

Contributes to species specific learned motor control and built in reflex control for highly skilled movements

Plays roll in skilled movements, higher mental functions, memory, emotion, cognitive, linguistic function

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2
Q

BG is NOT involved with

A

Movement initiation

Direct protections to LMN

UMN symptoms

Lesions induced paralysis

Spinal motor neuron activity or cranial

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3
Q

BG lesions cause

A

Inhibitory control

Involuntary movements

Dyskinesia, bradykinesia, hypokinesia, akinesia, dystonia

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4
Q

BG lesions

A

BG nuclei communicate to and from motor cortex on ipsilateral side

Symptoms would be contralateral

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5
Q

Structures of BG

A

Caudate nucleus, putamen, and globus pallidus

Functionally relates nuclei- subthalamus, substantia nigra

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6
Q

Primary BG neurotransmitters

A

Glutamate

Dopamine

GABA

Acetylcholine

Substance P

Enkephalin

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7
Q

BG First loop

A

Projections from sensorimotor and prefrontal cortex to neostriatum, GP, thalamus, and MC

Incorporation of integrated BG projections to neocortex

Most central

Motor impulses from sensorimotor and prefrontal to cn and putamen and GP int & ext
From here projection travel back to cortex after passing through VL and VANT thalamus

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8
Q

BG loop 2

A

Bidirectional projections connecting striatum to substantial nigra

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9
Q

BG loop 3

A

GP ext projections to sunthalamic nucleus and projections back to GP int

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10
Q

BG loop 4

A

Intralaminar and pontoreticular projections to striatum

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11
Q

Striatum

A

Caudate nucleus and putamen

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12
Q

BG is important for

A

Cognition

Personality

Refining motor activity

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13
Q

BG diseases cause

A

Loss of precision and inhibitory control

Loss of adequate inhibitory control on MC leading to involuntary motor behavior

Dyskinesia, bradykinesia, chorea, tremor, and impaired postural positions

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14
Q

Signs of BG dynfunctioming

A

Athetosis

Buccofacial muscles

Hemiballism

Chorea

Tremor

Dystonia

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15
Q

Athetosis

A

Sow involuntary twisting of axial and speech muscles with hypertonic

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16
Q

Hemballism

A

Forceful swinging her key and sudden movements of arms and legs

Subthalamic nucleus- suspected site for BG dysfuntionjng

17
Q

Chorea

A

Rhythmic quick and graceful looking involuntary movements

18
Q

Sydenham chorea

A

Post infections condition appearing in childhood between ages 5-13 years after streptococcal infection and fever

19
Q

Huntington chorea

A

Progressive neurologic condition with dementia, dysarthric speech, and personality change

Caudate degeneration leading to depletion of striatal cholingeric and GABAergic neurons

Disinhibition induced involuntary motor movements of chorea

Caudate nucleus and protein gal cortical atrophy suspected sites

Autosomal dominant disease

Adult onset

50% chance inheritance

20
Q

Caudate nucleus

A

Suspected site BG dysfunctioning chore

21
Q

Tremor

A

Constantly alternating motor activity in one or more part of body

22
Q

Resting tremor

A

Degenerative changes in substantial nigra PD

23
Q

Intention tremor

A

Approaching voluntary movements (cerebellar lesions)

24
Q

Associated symptoms with tremor (BG Dysfunctioning)

A

Masked face

Infrequent blinking

Slow
Movements

Disequilibrium

Stopped posture

Dysarthria

Dysphasia

25
Dystonia
Torticollis- lateral fixation of neck Musculorum deformAns- sustained involuntary movements of axial and limb muscles Tics- common dyskinesia behaviors like throats clearing, sniffling, excessive blinking Gilles de lA Tourette syndrome- hypersensitive dopMinergic receptors
26
Lesion of globus pallidus and corpus striatum (putamen)
Athetosis Toxicity, striatAl degeneration, and hypoxia owning to carbon monoxide poisoning
27
Subthalamic nucleus lesion
Ballism Stroke or denervation
28
Striatum lesion
Chorea Huntington chorea
29
Substantial nigra lesion
Dyskinesia Akinesia Bradykinesia Hypokinesia Tremor Parkinson's
30
BG diseases
Parkinson's Resting tremor Cogwheel muscular rigidity Bradykinesia Loss of postural reflexes Paucity of facial expressions Shuffling gait
31
BG disease treatment
L-dopa Deep brain stimulation Pallidotomy
32
Deep brain stimulation
Intralaminar or subthalamic stimulation
33
Pallidotomy
Or STN stimulation to reduce inhibitory output from GPM thereby facilitating movement
34
Tardive dyskinesia
Involuntary movements of facial and lingual muscles from psychotropic drugs Drugs used to treat mental illness
35
Wilson disease
Hepatolenticular degeneration Progressive disease (10-25 years onset) Metabolism Degeneration of BG cirrhosis of liver Muscular rigidity, tremor dynarthria and progressive dementia Treatment- diet and medication
36
Progressive Supra unclear palsy- brain stem cellular degeneration
Symptoms- initial- gaze palsy and imbalance Late- bradykinesia m, impaired Gait control, facial grimaces, dysarthria, and dysphasia Personality changes- socially withdrawn with possible cognitive impairments Treatment- l-dopa
37
BG and psychiatric disorders
Neurotransmitter dysfunctions in associated psychiatric illness High incidence of depression Parkinsonsims High depression and suicide Depression and altered personality Altered dopaminergic protections- Tourette and schizophrenia