Quiz Answers Midterm Flashcards
The blood brain barrier is most permeable to what kind of molecule?
small, lipid-soluble
The central nervous system (CNS) is comprised of
the brain and the spine
Which of the following is NOT a part of the “reward circuit”?
A. frontal lobe
B. tectum
C. ventral tegmental area (VTA)
D. nucleus accumbens
B. tectum
Which division of the nervous system controls bodily organs, glands, ducts, and pupils?
A. somatic
B. enteric
C. central
D. autonomic
D. autonomic
What division of the nervous system controls the gut?
A. enteric
B. central
C. somatic
D. autonomic
A. enteric
What ionic movement begins an action potential?
A. exit of sodium ions
B. exit of potassium ions
C. entrance of sodium ions
D. entrance of potassium ions
C. entrance of sodium ions
An ion channel that contains a receptor site is called
an ionotropic receptor
Which of the following is NOT a monoamine?
A. dopamine
B. glutamate
C. norepinephrine
D. serotonin
B. glutamate
Which neurotransmitter is particularly important for mood, appetite, and sleep?
A. serotonin
B. GABA
C. glutamate
D. dopamine
A. serotonin
Drugs administered “sublingually” (under the tongue) and drugs administered orally are absorbed mostly in the ____ and ____ respectively.
A. mouth; stomach
B. small intestine; large intestine
C. stomach; small intestine
D. mouth; small intestine
D. mouth; small intestine
Which route of administration is characterized as “enteral”?
A. topical
B. inhalation
C. injection
D. oral
D. oral
All of the following drug attributes decrease the likelihood of drug absorption EXCEPT:
A. small size
B. low lipid-solubility
C. high water-solubility
D. large size
A. small size
What are the two main differences between capillaries in the periphery and capillaries in the brain?
capillaries in the brain have tighter junctions & are surrounded by membranes of astrocyte cells
Of the following, which is the most dangerous mode of drug administration?
A. subcutaneous
B. topical
C. intramuscular
D. intravenous
D. intravenous
The degradation of drugs by enzymes present in the gastrointestinal tract and liver is known as:
first-pass metabolism
Most drugs are excreted via the
kidneys
The time for the plasma level of a drug to fall by 50% is called the
elimination half-life
The “steady-state” concentration of a drug (the stable level achieved in blood with repeated, regular dosing) is
achieved when the amount of drug administered per unit time equals the amount eliminated per unit time
The ability of liver enzymes to degrade a drug more efficiently in the continued presence of the drug is termed
metabolic tolerance
“Pharmacodynamic” tolerance occurs in the ____; “metabolic” tolerance occurs in the _____.
synapse/neuron; liver
The term placebo is best described as
A pharmacologically inactive substance that elicits a significant therapeutic response
A drug that is more potent than another drug has
a smaller ED50
Most side effects are:
A. predictable and serious
B. predictable and mild
C. unpredictable and mild
D. unpredictable and serious
B. predictable and mild
The therapeutic index (TI) refers to the
relative safety of a drug