Final exam select topics-neurotox Flashcards

1
Q

neuropathy

A

irreversible death, apoptosis, necrosis (only some myelin left, no axon)

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2
Q

axonopathy + where repaired

A

repaired in PNS not CNS, change in cell body too

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3
Q

myelinopathy + where repaired

A

some repaired in PNS not CNS, slows conduction

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4
Q

nissl substance

A

clusters of ribosomal complex

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5
Q

what disease foes trimethyltin chloride make

A

limbic-cerebellar syndrome (neuropathy)

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6
Q

what is a main way that trimethyltin chloride causes limbic-cerebellar syndrome (neuropathy)

A

stannins

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7
Q

what are stannins + where are they

A

proteins associated with ER and mito

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8
Q

where are high levels of stannins

A

limbic cerebellar areas, hippo amyg

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9
Q

what do stannins contain

A

cytoplasmic metal binding domain

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10
Q

how does trimethyltin chloride affect stannins

A

they bind, causes Ca++ flux then initiates apoptosis

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11
Q

what does rayon and CS2 cause (simple)

A

axonopathy

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12
Q

what does CS2 do generally

A

modified proteins

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13
Q

who does CS2 cause irreversible damage to

A

amino groups (draw it out)

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14
Q

who does CS2 cause reversible damage to

A

sulfhydryl groups (draw it out)

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15
Q

what are 2 CS2 markers

A

valine-lysine and lysine-lysine thiourea

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16
Q

where does lysine-lysine thiourea happen

A

globin

17
Q

where does valine-lysine thiourea happen

A

spectrin

18
Q

what reaction happens to form acrylamide (what 2 things join)

A

asparagines and reducing sugars (Maillard reaction)

19
Q

how is acrylamide metabolized + what into

A

CYP2E1 into glycidamide

20
Q

what is the deal with glycidamide

A

its a much stronger electrophile than acrylamide (can modify proteins, DNA)

21
Q

what happens to glycidamide

A

it is converted into glyceramide (non toxic) or detoxed by GSH

22
Q

so what are the 2 compounds in order that acrylamide can become

A

glycidamide then glyceramide

23
Q

what are the steps to make acrylamide (think maillard, 4 steps)

A
  • asparagine and reducing sugar join
  • water loss to make Schiff base
  • amadori rearrangement to make amadori compound
  • amadori loses CO2 to make acrylamide
24
Q

what is the main acrylamide toxicity (1 main thing)

A

forms adducts with proteins, esp with SH groups

25
Q

what are 3 possible acrylamide mechanisms

A
  • defective kinesin based anterograde transport
  • mitochondrial disfunction (energy deficit)
  • direct effect on NT release
26
Q

what kind of toxicity does Domoic acid cause

A

amnesic shellfish poisoning

27
Q

what causes amnesic shellfish poisoning

A

domoic acid

28
Q

what is the structure of domoic acid and what is it similar to

A

tricarboxylic acid, structural analog to kainic acid

29
Q

what is the mechanism of domoic acid

A

stimulates kainate glutamate receptors to conduct Ca++ into cells (excitatory)

30
Q

does domoic acid cause receptor desensitization

A

no

31
Q

what part of brain does domoic acid preferentially effect

A

hippocampus

32
Q

what are the 2 stages of domoic acid poisonings

A

24 hours is GI

48 is neurolgical

33
Q

what are the 4 compounds that happen after CS2 modified a protein

A

dithiocarbamate, isothiocyonate then either dithiocarbamate ester or thiourea linkage