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Pharmacology Test Bank Questions and Answers

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  • Course
  • Pharmacology
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  • Pharmacology

The multi drug resistance proteins (or p-glycoproteins) can protect liver and kidney cells by exporting harmful chemicals against a concentration gradient in an energydependent manner. WThe multi drug resistance proteins (or p-glycoproteins) can protect liver and kidney cells by exporting harm...

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  • August 16, 2024
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  • Pharmacology
  • Pharmacology
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Pharmacology Test Bank Questions
and Answers

The pKa (for the COOH group) of each of the three drugs is as follows: thyroxine =

3.0, mesothyroxine = 4.0, neothyroxine = 5.0. Of these, which will be absorbed to the

greatest extent from the stomach (pH = 1.0)?

✓ ~~~ neothyroxine



The multi drug resistance proteins (or p-glycoproteins) can protect liver and kidney

cells by exporting harmful chemicals against a concentration gradient in an energy-

dependent manner. What is this called?

✓ ~~~ active transport



Phase II conjugates typically have the following property/properties

✓ ~~~ rapidly excreted in the urine



A drug with a half-life of 2 hours is administered by continuous intravenous infusion.

How long will it take for the drug to reach 50% of its steady state concentration?

✓ ~~~ 2 hours



Caffeine is eliminated primarily by metabolism and with first order kinetics. The half-

life of caffeine varies significantly with individuals, but is on average 5.0 hours. The

volume of distribution is 0.60 L/kg. Joe has a mass of 70 kg and is an average

subject with regard to caffeine pharmacokinetics. He has a regular habit of

consuming a cup of coffee (85 mg of caffeine) at 8 am.

,What is the clearance value (CL) of caffeine in a normal individual?

✓ ~~~ 0.083 L/hr/kg



Which of the following routes is most likely to be affected by the first-pass effect?

✓ ~~~ oral



A drug, given as a 150 mg single dose, results in a peak plasma concentration of 10

ug/mL. The apparent volume of distribution is (rapid distribution and negligible

elimination prior to measuring the peak plasma level):

✓ ~~~ 15 L



Which of the following are routes of drug clearance?

-renal

-sweat

-intestines

✓ ~~~ all of the above



What factor(s) may reduce drug bioavailability?

-gastric acid instability

-first-pass affect

-exposure to digestive enzymes

✓ ~~~ all of the above



What type of receptor is the muscarinic receptor?

, ✓ ~~~ G-protein coupled receptor



For a cholinesterase modified by an organophosphate compound (e.g. soman), what

is the time-dependent dealkylation process called yielding an enzyme refractory

toward reactivation?

✓ ~~~ aging



Muscarinic receptors bind

✓ ~~~ acetylcholine



Which of the following is a clinical use for a muscarinic agonist?

✓ ~~~ "switching on" the urinary tract after surgery



Indirect cholinergic agonists cause

✓ ~~~ inhibition of acetylcholinesterase and a corresponding increase in the synaptic
acetylcholine levels



Which of the following is characteristic of the sympathetic nervous system?

✓ ~~~ responded predominate during physical activity or when experiencing fright



A patient with an acute attack of glaucoma is treated with pilocarpine. The primary

reason for its effectiveness in this condition is its:

✓ ~~~ ability to lower intraocular pressure



Put the following steps in the correct order for neurotransmission at the cholinergic

neuron

, ✓ ~~~ 1. acetylcholine is synthesized from choline and acetyl-CoA
2. acetylcholine is released from storage vesicles into the synaptic cleft

3. acetylcholine is synthesized from choline and acetyl-CoA

4. acetylcholine is degraded by acetylcholinesterase




The autonomic nervous system innervates all of these except

✓ ~~~ skeletal muscle



A soldiers' unit has come under attack with a nerve agent. The symptoms exhibited

are skeletal muscle paralysis, profuse brachial secretions, miosis, bradycardia, and

convulsions. The alarm indicates exposure to an organophosphate. What is the

correct treatment?

✓ ~~~ administer atropine and 2-PAM (pralidoxime)



a study examining how a drug is distributed throughout the body and how the drug is

changed before eliminated is an example of

✓ ~~~ pharmacokinetics



knowing that all three drugs interact with the same receptor, which drug is a

competitive antagonist?

✓ ~~~ C on graph



rate the following drugs labeled 1-4 based on increasing efficacy

✓ ~~~ 2<4<1<3

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