Misc. Neuro disorders Flashcards

(55 cards)

1
Q

what is the purpose of astrocytes

A

form contacts between neuronal surfaces and and blood cells. transports nutrients and metabolites
IMPORTANT PART OF BLOOD BRAIN BARRIER

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2
Q

what is the function of microglia

A

clear cellular debris

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3
Q

what is the function of non-myelinating Schwann cells

A

neuronal metabolic support and regrowth within PNS

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4
Q

what is the function of satellite glial cells

A

surround the sensory, sympathetic, parasympathetic nerves to help protect and promote cellular communication

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5
Q

what is the function of myelin

A

segments of lipid wrap that insulates the axon - allows for saltatory conduction

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6
Q

oligodendrocyte location

A

CNS

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7
Q

Schwann cell location

A

PNS

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8
Q

what is a deymelination of oligodendrocytes

A

Multiple sclerosis

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9
Q

what is demylination of schwann cells

A

Guillain-Barre

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10
Q

what is MS

A

degenerative, chronic disease
autoimmune inflammatory state leading to demyelination - will occur over hours to days
affects to myelin of the CNS (oligodendrocytes)

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11
Q

what is the pathophysiology of MS

A

genetic predisposition with environmental triggers
HLA-DRB mutation - causes abnormal response to MHC proteins

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12
Q

what is the etiology of MS

A

F>M
low vitamin D
viral infections

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13
Q

what is EBV

A

Epstein Barr virus
type of herpes virus - asymptomatic or may cause mono

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14
Q

what is necessary for MS to develop

A

EBV - since EBC antigen looks very similar to myelin and demyelination during the inflammatory response to autoimmune reaction

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15
Q

what type of cell mediated disease is MS

A

B-cell mediated disease

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16
Q

how does MS start

A

starts with clinically isolated syndrome
must occur for > 24 hours
typically recover (remyelination)

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17
Q

what is gliosis

A

scar tissue of glial cells

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18
Q

what is the most common symptom of MS

A

optic neuritic - can also be spinal cord syndrome, brain stem syndrome, cerebellar syndrome

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19
Q

what is possible presentation of MS

A

may present with spasticity, muscular weakness, sensory changes, incontinence (if autonomic system involved, ataxia(cerebrellum))

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20
Q

as MS progressed what is most likely to be affected

A

cognitive deficits (memory, attention, psychiatric, depression, dementia)

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21
Q

what are the MS classifications

A

relapsing remitting
primary progressive
secondary progressive
progressive relapsing

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22
Q

what is relapsing remitting MS

A

most common
will have recurrent relapses during inflammatory activation
may or may not have symptoms
typically worsens clinically over time - progressive disability

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23
Q

what environmental factor affects MS

24
Q

what is primary progressive MS

A

more consistent worsening of symptoms without relief

25
what is secondary progressive MS
relapsing turned progressive
26
what is progressive relapsing MS
will have consistent worsening with flairs
27
what can be repaired, axons or myelin
myelin can be repaired
28
what Cranial nerves have oligodendrocytes
CN1 and CN2
29
what is Marcus Gun pupil
vasodilation with light sign of optic neuritis
30
what part of your brain makes you emotional
limbic system
31
what is function of the limbic system
mediates emotional response with memory/learning visceral reaction
32
what makes up the limbic system
Basal Ganglia, hypothalamus, thalamus, amygdala and hippocampus
33
what is the function of the basal ganglia
part of the limbic system includes caudate and putamen (together = striatum) these pathways help with motor, emotional and learning reward
34
what is the cause of tourettes disorder
lack of inhibiting factors of the limbic and motor syndrome lead to motor and phonic tics - specifically the cortico-striatal-thalamic-cortical (mesolimbic) circuit which is important in decision making, regulation of affect, goal-directed behaviors
35
what is used to ID changes in the structural as well as metabolic processes in pts with tourettes
functional imaging
36
what portion of the brain is triggered just prior to a tourettes tic
insula implicated which typically helps to monitor sensation/urges changes in basal ganglio functionally
37
what is structurally smaller in patients with tourettes
decrease in size of the caudate which is part of the basal ganglion and helps to organize our motor movements
38
what is decreased wtihin the basal ganglio
GABA - creates stimulating effect without GABA receptor
39
when is the peak symptom of tourettes
around puberty with many patients and resolving their ticks after puberty
40
how is ICP assessed
lumbar puncture
41
what is NPH
Normal pressure hydrocephalus normal flow of CSF, no constriction or blockage of flow of the CSF
42
what is the presentation of NPH
dementia, gait alteration, incontinence gait is the first thing affected
43
how can NPH be treated/reversed
VP shunt
44
what is the cause of NPH
Idiopathic or secondary to hemorrhage or infection
45
what are the cause of Idiopathic NPH
HTN, CAD, PAD increase risk decreased absorption increased venous pressure
46
what is the triad of NPH
wacky, wobbly, wet dementia, wide gait, urinary incontinence
47
what is the most common NMJ disorder
Myasthenia gravis
48
what is M. gravis
autoimmune response to the Ach receptors of NMJ antibodies attack ocular, respiratory, head/neck and limb muscles
49
what do antibodies target in M. gravis
AChR antigen
50
what type of hypersensitivity reaction is M. gravis
type 2 tissue specific hypersensitivities
51
what is ALS
amytrophic lateral sclerosis progressive neurodegenerative disease - ultimately fatal
52
what is degenerated in ALS
the upper and lower motor neurons - causes thinning of spinal cord and causes muscle atrophy
53
where does ALS begin
neck/head muscles, limbs and then respiratory muscles
54
what causes fatality in ALS patients
respiratory compromise
55
what is decreased in uptake in ALS
decreased glutamate uptake which causes excitotoxicity and calcium goes crazy and triggers microglia to cause inflammation and damage axons