Exam 2 Flashcards

1
Q
Administering a syustemic antidote that acts like a chemical "claw" to bind and accelerate elimination of absorbed metals after exposure is referred to as:
A) competitive inhibition	
B) chelation
C) phase 1 biotransformation
D) neutralization
A

B) chelation

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2
Q
Detectable and measurable exogenous environmental chemicals, such as lead, in a person's (or animal's) blood and/or urine sample, represents a biomarker of
A) effects
B) elimination
C) excretion
D) exposure
A

D) exposure

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3
Q
Detectable and measurable elevation of endogenous chemicals, such as liver enzymes, in a person's (or animal's) blood sample, represent a biomarker of:	
A) effects
B) elimination
C) excretion
D) exposure
A

A) effects

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4
Q
The most common biological matrix to sample and analyze for systemically absorbed toxic chemicals, their metabolites, and/or related biochemical changes is
A) saliva
B) adipose tissue	
C) hair		
D) blood
A

D) blood

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5
Q

**Select which of the following is NOT a biomarker from the perspective of clinical toxicology:
A) cadmium in urine
B) arsenic in hair
C) chlorinated hydrocarbons (e.g., PCBs) in adipose tissue
D) chelator in blood

A

D) chelator in blood

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6
Q
**One matrix to consider for screening of a person's exposure to a highly volatile and relatively blood (water) insoluble environmental chemical such as the organic solvent benzene is:
A) adipose tissue
B) hair
C) saliva
D) exhaled air
A

D) exhaled air

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7
Q

One clinical toxicology approach is to collect and analyze a biologic matrix such as blood or urine for a chemical parent compound to determine if internal exposure occurred, but instead, or as well, internal exposure can be documented by measuring:
A) another parent compound
B) a biotransformed parent compound or molecule
C) an antidote
D) a physiological response

A

B) a biotransformed parent compound or molecule

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8
Q

**Absorption across the skin
A) occurs equally well across the skin from all parts of the body
B) occurs predominantly by active transport across the stratum corneum
C) involves passive diffusion across the dried, keratin-filled cells of the stratum corneum
D) occurs predominantly via passive diffusion across the hair follicles, sweat ducts, and sebaceous glands

A

C) involves passive diffusion across the dried, keratin-filled cells of the stratum corneum

**answer was C) on the last test, and D) on this one (occurs predominantly via passive diffusion across the hair follicles, sweat ducts, and sebaceous glands). In the review session, Tyler stated that C) was in fact the better answer. Though absorption across the skin can occur across hair follicles/sweat ducts/sebaceous glands, crossing the stratum corneum is more common. Therefore since D) says “predominantly,” it’s factually incorrect

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9
Q

In primary irritation testing
A) the test animal is always given an analgesic
B) the test chemical is placed on normal and abraded skin under a patch for 24h
C) the test animal is usually a rat
D) the skin is evaluated only once

A

B) the test chemical is placed on normal and abraded skin under a patch for 24h

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10
Q

**The skin:
A) is a fairly permeable barrier to environmental toxicants
B) is not responsive to UV light
C) is fairly static as stratum corneum cells typically are not replaced with any regularity
D) is in a constant state of change as statum corneum cells typically are replaced monthly

A

D) is in a constant state of change as statum corneum cells typically are replaced monthly

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11
Q

Acute dermal irritation may be defined as:
A) wheal and flair reactions induced very shortly after cutaneous exposure to chemicals
B) reversible chemical-induced changes in sebaceous gland secretions
C) a local reversible inflammation of normal living skin that occurs shortly after a single exposure of the skin to a toxicant
D) a toxic effect resulting from DNA damage

A

C) a local reversible inflammation of normal living skin that occurs shortly after a single exposure of the skin to a toxicant

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12
Q

Which of the following mechanisms does NOT apply to percutaneous toxicity?
A) biliary excretion of the toxicant
B) integrity of the skin to the toxicant
C) physiochemical properties of the toxicant
D) vehicle used to dissolve the toxicant

A

A) biliary excretion of the toxicant

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13
Q

The blood-brain barrier:
A) is a semi-permeable barrier that excludes molecules great than 40kD
B) is found around all parts of the brain and spinal cord
C) is formed by having keratinocytes surround the neurons
D) is not an effective barrier

A

A) is a semi-permeable barrier that excludes molecules great than 40kD

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14
Q

**Axons:
A) are involved in receiving messages from other nerve cells
B) are short extensions of the cell body of the neuron
C) are fairly tolerant of the toxic effects of chemicals
D) are involved in the synthesis and release of neurotransmitters

A

D) are involved in the synthesis and release of neurotransmitters

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15
Q

**The autonomic nervous system normally does NOT function to:
A) control heart rate
B) stimulate breathing
C) stimulate skeletal muscle contractions
D) control pupil diameter

A

C) stimulate skeletal muscle contractions

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16
Q
Which of the following is a toxic effect on the nervous system? 	
A) nephropathy	
B) cardiomyopathy	
C) retinopathy	
D) axonopathy
A

D) axonopathy

17
Q

Which of the following morphologic descriptions of nerve damage is accurate?
A) loss of the white layer around myelinated neurons indicates myelinopathy
B) Nissl substance is increased markedly in neuronopathy
C) damage to the cell body is called axonopathy
D) loss of the white layer around myelinated neurons indicated a transmission defect

A

A) loss of the white layer around myelinated neurons indicates myelinopathy

18
Q

**Which of the following is NOT a criterion for a chemical to be called a neurotransmitter?
A) the chemical must cause the same response as stimulation of the nerve
B) synthesis of the chemical must be able to occur in the nerve
C) the chemical must be present in all nerves
D) the nerve must possess the ability to terminate the action of the chemical

A

C) the chemical must be present in all nerves

19
Q
Toxicant effects on the nervous system do NOT include:
A) alteration in neurotransmission	
B) nephropathy
C) axonopathy
D) demyelination
A

B) nephropathy

20
Q

**Particles approximately 1 micro-meter in diameter typically deposit in which part of the respiratory system?

A

Alveoli

21
Q

True or False: Asthma is characterized by open airways and easy gas exchange.

A

False

22
Q

In the conducting airway, what are the anatomic structures that induce protective effects?
1.
2.
3.

A

mucous
cilia
mucous layer

23
Q

What are the anatomic structures of the blood-gas barrier?
1.
2.
3.

A

epithelium
interstitial tissue
endothelium

24
Q

Which cells produce pulmonary surfactants?

A

alveolar type II cells

25
Q

**What is the definition of PM2.5?

A

ambient particles with diameters less than 2.5 micrometers

26
Q

**The critical effect is defined as…
A) The first adverse effect of a chemical that occurs as dose increases
B) The first effect of a chemical that occurs as dose increases
C) The most significant effect that is seen upon a clinical evaluation of a patient
D) The most severe effect that a chemical causes in a population of sensitive individuals

A

A) The first adverse effect of a chemical that occurs as dose increases

27
Q

Clear advantages and disadvantages exist in the use of a benchmark dose (BMD). Which item below is a disadvantage?
A) uses responses near the range of observation
B) includes a measure of variability in the response
C) determines consistent measure of response
D) applies to fewer, more robust, toxicity data sets
E) accounts for more dose response of critical effect

A

D) applies to fewer, more robust, toxicity data sets

28
Q

**Toxicology testing in the 21st century will include in silico testing of chemicals. Advantages are numerous when compared with standard bioassays, but some problems still need to be worked out. These problems include:
A) Cheaper and high throughput
B) Predictive analyses, more informative, and efficient
C) Minimize animal testing and focus on relevant dose levels
D) Human cells- minimal interspecies extrapolation

A

B) Predictive analyses, more informative, and efficient

29
Q

Research needs for the in silico testing of chemicals include all but which of the following:
A) Phenotypic anchoring for clinical, critical, or adverse effects
B) Markers for common critical effects, such as decreased body weight and models for specific “itices”- e.g., neurotoxicity
C) Address communication among tissues; endocrine effects, in vitro and in vivo extrapolation
D) Incorporate metabolism, differences in individauls, and durations
E) Testing for non-volatile chemicals

A

E) Testing for non-volatile chemicals

30
Q

**A properly executed assessment of risk considers all of the following EXCEPT
A) Evaluation of data from human exposures
B) Evaluation of data from laboratory animal studies
C) Evaluation of public perception of risks versus benefits
D) Evaluation of data regarding chemical production

A

D) Evaluation of data regarding chemical production

31
Q

Quantitative risk assessment:
A) is always influenced by political and financial concerns
B) ascertains the quality of the available experimental data
C) readily places little importance on animal data when scanty human data are available
D) readily ignores all data that may contain flaws from their collection

A

B) ascertains the quality of the available experimental data

32
Q
Cancer is a group of diseases characterized by uncontrolled what?
A) Pain
B) Cell proliferation
C) Mitochondrial growth
D) Gene expression
A

B) Cell proliferation

33
Q

Which of the following established cancer risk factors combinations are attributable to the most cancer deaths?
A) Environmental pollution and tobacco
B) Tobacco and excess weight/obesity
C) Excess weight/obesity and alcohol
D) Family history (hereditary) and UV radiation

A

B) Tobacco and excess weight/obesity

34
Q
Which of the following is NOT a feature of genotoxic carcinogens?
A) mutagenic 	
B) can be complete carcinogens 	
C) no threshold	
D) no direct DNA damage
A

D) no direct DNA damage

35
Q

Promoters:
A) Cause a change in DNA (i.e., mutations)
B) Increase expression of genes associated with cell proliferation
C) Induce DNA repair enzyme systems
D) Are effective modifier of carcinogenesis with a single exposure

A

B) Increase expression of genes associated with cell proliferation

36
Q
There can be a long period of time between exposure to carcinogens and the clinical appearance of cancer. This is known as the:
A) Treatment window
B) Initiation period
C) Latency period
D) Rest period
A

C) Latency period

37
Q
**A benign tumor found within the bone is known as a:	
A) Osteosarcoma
B) Osteoma
C) Fibroma
D) Squamous cell adenoma
E) Squamous cell carcinoma
A

B) Osteoma

38
Q

Which of the following is NOT a characteristic of cancer compared to normal cells?
A) Large number of dividing cells
B) Large, variable shaped cells
C) Small cytoplasmic volume relative to nuclei
D) Variation in cell size and shape
E) Well organized arrangement of cells

A

E) Well organized arrangement of cells