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PUBH 6011 FINAL EXAM QUESTIONS AND ANSWERS VERIFIED 100% CORRECT

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PUBH 6011 FINAL EXAM QUESTIONS AND ANSWERS VERIFIED 100% CORRECT Exposure pattern influencing dose response - ANSWER- acute toxicity: happens quickly - usually after 1 dose - include death, CNS effects, irritation, etc. Chronic: - result of prolonged exposure, usually lower doses than acute - organ damage, cancer - eventually it will build up to a point where the adverse effect occurs frequently little relationship between the two Pharmacokinetics influencing dose response - ANSWER- can differ by species, sex, age, nutrition, disease, enzyme induction (prior exposure) - how the body responds to a specific dose/exposure DDT LD50 in rats - ANSWER- - newborn rats have a higher tolerance for DDT - the lower the LD50, the more toxic the chemical is (bc it takes less of it to have effects) - age influences toxicity/response in either direction Species and strain in dose response - ANSWER- - can differ between strains due to different mechanisms of action/different receptors between species - common to assume that humans are the most sensitive when studying and use the most sensitive species to begin studying the chemical LD50 - ANSWER- - dose (mg/kg) lethal to 50% of test animals - determined orally, through inhalation or by dermal exposure LC50 - ANSWER- - concentration (in ppm or mass/volume) lethal to 50% of test animals - something in the water, air, etc. where you can measure the concentration in the environment Subchronic/chronic tox testing - ANSWER- - concerned with long term exposure to lower doses - test for damage to certain organs - damage to functional systems (neuro, immuno, etc.) - test for carcinogenicity Mechanic studies - ANSWER- - study of potential models of action in lab animals (in vivo) or with isolated tissues, cells or components (in vitro) strengths: - compound specific info - understanding biology should improve problems: - difficult to rule out alternative theories - lack necessary data for humans Assessing risks - ANSWER- - personal: risk of walking, driving, etc. - public health - occupational health: setting workplace standards - architects: risk of structure injuring people, earthquakes - medical: risk of side effects from new drugs - dept of transportation: traffic, hazardous material transport actuarial risks - ANSWER- - based on experience with the same risk - predictions made with great deal of precision - diseases, auto accidents, etc. modeled risks - ANSWER- - based on data and theory - predictions subject to uncertainty - cancer risk from chemicals, climate change, etc. - don't have data exactly on what we are interested in/may not predict exactly Risk assessment paradigm - ANSWER- - hazard identification: which adverse effects? - dose-response: how much does it take? - exposure assessment: how much do people take in?; usually the level that you would manage at bc you can't change the toxicity of the thing itself - risk characterization: estimate magnitude of risk and uncertainty Hazard identification - ANSWER- - physical/chemical properties - epidemiology - toxicology - asks what harmful effects is the agent capable of causing? Types of adverse effects - ANSWER- - acute toxicity - irritation - corrosivity - sensitization - repeated dose toxicity - mutagenicity - carcinogenicity - toxicity for reproduction

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PUBH 6011 FINAL EXAM QUESTIONS AND ANSWERS
VERIFIED 100% CORRECT

Exposure pattern influencing dose response - ANSWER- acute toxicity:
happens quickly
- usually after 1 dose
- include death, CNS effects, irritation, etc.

Chronic:
- result of prolonged exposure, usually lower doses than acute
- organ damage, cancer
- eventually it will build up to a point where the adverse effect occurs

frequently little relationship between the two

Pharmacokinetics influencing dose response - ANSWER- can differ by
species, sex, age, nutrition, disease, enzyme induction (prior exposure)

- how the body responds to a specific dose/exposure

DDT LD50 in rats - ANSWER- - newborn rats have a higher tolerance
for DDT
- the lower the LD50, the more toxic the chemical is (bc it takes less of
it to have effects)
- age influences toxicity/response in either direction

Species and strain in dose response - ANSWER- - can differ between
strains due to different mechanisms of action/different receptors
between species
- common to assume that humans are the most sensitive when studying
and use the most sensitive species to begin studying the chemical

,LD50 - ANSWER- - dose (mg/kg) lethal to 50% of test animals
- determined orally, through inhalation or by dermal exposure

LC50 - ANSWER- - concentration (in ppm or mass/volume) lethal to
50% of test animals
- something in the water, air, etc. where you can measure the
concentration in the environment

Subchronic/chronic tox testing - ANSWER- - concerned with long term
exposure to lower doses
- test for damage to certain organs
- damage to functional systems (neuro, immuno, etc.)
- test for carcinogenicity

Mechanic studies - ANSWER- - study of potential models of action in
lab animals (in vivo) or with isolated tissues, cells or components (in
vitro)

strengths:
- compound specific info
- understanding biology should improve

problems:
- difficult to rule out alternative theories
- lack necessary data for humans

Assessing risks - ANSWER- - personal: risk of walking, driving, etc.
- public health
- occupational health: setting workplace standards
- architects: risk of structure injuring people, earthquakes
- medical: risk of side effects from new drugs
- dept of transportation: traffic, hazardous material transport

,actuarial risks - ANSWER- - based on experience with the same risk
- predictions made with great deal of precision
- diseases, auto accidents, etc.

modeled risks - ANSWER- - based on data and theory
- predictions subject to uncertainty
- cancer risk from chemicals, climate change, etc.
- don't have data exactly on what we are interested in/may not predict
exactly

Risk assessment paradigm - ANSWER- - hazard identification: which
adverse effects?
- dose-response: how much does it take?
- exposure assessment: how much do people take in?; usually the level
that you would manage at bc you can't change the toxicity of the thing
itself
- risk characterization: estimate magnitude of risk and uncertainty

Hazard identification - ANSWER- - physical/chemical properties
- epidemiology
- toxicology
- asks what harmful effects is the agent capable of causing?

Types of adverse effects - ANSWER- - acute toxicity
- irritation
- corrosivity
- sensitization
- repeated dose toxicity
- mutagenicity
- carcinogenicity
- toxicity for reproduction

, IARC Carcinogen Classification - ANSWER- - organization of WHO,
mission to review the evidence for carcinogenicity of chemicals
- human evidence is almost always epi data
- always none, inadequate, sufficient, limited evidence

Exposure assessment - ANSWER- - how much of the substance of
concern are people exposed to?
- what are the sources of exposure?

Exposure and dose - ANSWER- exposure: air breathed, water ingested,
dermal contact; usually measured as concentration

dose: quantity taken into the body
- administered dose: amount taken into the body (ie pill)
- absorbed dose: crosses a biological barrier into the body

Measuring and modeling exposure - ANSWER- measured:
- more precise
- more expensive
- source must be present

modeled:
- rely on models using chemical and climate information
- require many assumptions
- models imprecise and rarely validated
- allow better incorporation of time into exposure estimates

exposure pathways - ANSWER- - inhalation, absorption, ingestion

- air, soil, water, diet

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