Test 4: 45 principles part 1 Flashcards

1
Q

most common toxins of tremorgenic mycotoxins

A

penitrem A (moldy walnuts)
roquefortine C (soft cheeses)

at least 20 mycotoxins have been identified as tremorgens- most commonly associated with penicillium species

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2
Q

tremorgenic mycotoxins cause intoxication in what type of animals

A

a bunch

dogs, cattle, sheep, rabbits, rodents, poultry

molds that lead to tremors

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3
Q

how does tremorgenic mycotoxins work

A

several proposed theories

May vary both between specific toxins and individual susceptible species

  • Penitrem-A inhibits the inhibitory neurotransmitter glycine in mice
  • Another tremorgen, verruculogen, reduces concentrations of GABA in the brain
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4
Q

treatment for tremorgenic mycotoxins

A

Diazepam and methocarbamol

if not responding to diazepam: barbiturates (pentobarbital)

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5
Q

how to decontaminate tremorgenic mycotoxin intoxication

A

sedate and gastric lavage if pt has not vomited

activated charcoal and a cathartic

sedation will decrease risk of tremor and ET tube will prevent aspiration

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6
Q

general treatment for tremorogenic mycotoxin poisoning

A
  • Thermoregulation
  • Treat for shock
  • Intravenous fluid support
  • Prognosis good with early and aggressive treatment
  • No long-term sequelae expected
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7
Q

1947 Federal Insecticide, Fungicide, and Rodenticide Act (FIFRA): Non-food, non-drug substances had to be shown to be —

A

safe and efficacious

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8
Q

alternate term for poison, any agent capable of producing a deleterious response in a biological system

A

toxicants

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9
Q

poison that originates from biological processes

A

toxin

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10
Q

Toxicity vs toxicosis

A

Toxicity = quantity or amount that causes a toxic effect

Toxicosis = disease state that results from exposure to a poison

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11
Q

threshold dose vs LD50 vs median lethal dose

A

Threshold dose = highest dose of toxicant at which toxic effects are not observed

Lethal dose 50% or LD50 = the dose at which 50% of the animals die

Median lethal dose (MLD) = used interchangeably with LD50

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12
Q

NOEL and NOAEL

A

no observed effect
level

no observed adverse effect level

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13
Q

LOEL and LOAEL

A

LOEL: lowest observed effect level

LOAEL: lowest observed adverse effect level

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14
Q

the — the therapeutic index, the safer the chemical

A

larger

TI= LD50/ED50

if large number, there is a wide dose that can be given before toxic effects

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15
Q

the smaller the standard safety margin the — the chemical

A

more dangerous

SSM= LD1/ED99

standard safety margin (SSM)= margin of safety (MoS)

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16
Q

chronic toxic effects may occur if chemicals —, toxic effects products are — or there is — between exposures

A

accumulate

irreversible

insufficient recovery time

17
Q

additive effect vs synergistic effect

A

additive: 2+3=5

synergistic: 2+3=20 (greater than the sum of the individual, occur if one chemical affects the solubility, binding, metabolism, or excretion of
the other

18
Q

potentiation

A

one otherwise non-toxic or only mildly-toxic chemical enhances the toxicity of another chemical

0 + 2 = 20

  • Isopropanol is not hepatotoxic, however enhances the hepatotoxicity of carbon tetrachloride
19
Q

antagonism can work in three ways

A

Physiologic – epinephrine antagonizes hypotensive effects of phenobarbital

Chemical – calcium EDTA complexes with lead

Metabolic – ethyl alcohol competes with ethylene glycol (EG), preventing EG’s activation to toxic metabolites

20
Q

for dose response what three assumptions are made

A
  • The chemical interacts with a molecule or receptor site to produce a response
  • The production of the response, or degree of response, is correlated to concentration of the chemical at that receptor site
  • The concentration of the chemical at the receptor site is related to the dose of chemical received
21
Q

hormesis

A

Some xenobiotics impart beneficial or stimulatory effects at low doses but have adverse effects at higher doses

selenium, Vit A

22
Q

cadmium will cause – is ingested, inhaled or touched

A

Oral exposure → renal lesions

Inhalation exposure → lungs 1st +/- kidneys

Dermal exposure → produces little if any toxicity

23
Q

Felines possess limited —capabilities, so must rely on the less- efficient sulfate & cysteine conjugation pathways compared to dogs

A

glucuronidation

24
Q

why are young animals usually more susceptible to toxins

A
  • GI mucosa and blood-brain barrier are less developed
  • Drug-metabolizing enzymes are generally less active
  • Higher proportions of body water and lower proportions of body fat influence distribution and storage of drugs and chemicals