Deck 1: Pharmacodynamics: Receptors and Concentration-Response Relationships

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Nalbuphine is an effective pain reliever because of its activity at mu-opioid receptors. However, if given to a patient who has recently received morphine (which also affects mu-opioid receptors) for postoperative pain, nalbuphine can worsen his or her pain. Thus nalbuphine is said to have what kind of activity at mu-opioid receptors?

A) Full agonist
B) Partial agonist
C) Competitive antagonist
D) Non-competitive antagonist
E) Allosteric modifier
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Question
The majority of medications available today act on which superfamily of cellular membrane receptor?

A) Ligand-gated ion channel
B) G-protein-coupled receptor
C) Receptor tyrosine kinase
D) Nuclear hormone receptor
E) Cytokine receptor
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Deck 1: Pharmacodynamics: Receptors and Concentration-Response Relationships
Nalbuphine is an effective pain reliever because of its activity at mu-opioid receptors. However, if given to a patient who has recently received morphine (which also affects mu-opioid receptors) for postoperative pain, nalbuphine can worsen his or her pain. Thus nalbuphine is said to have what kind of activity at mu-opioid receptors?

A) Full agonist
B) Partial agonist
C) Competitive antagonist
D) Non-competitive antagonist
E) Allosteric modifier
Partial agonist
The majority of medications available today act on which superfamily of cellular membrane receptor?

A) Ligand-gated ion channel
B) G-protein-coupled receptor
C) Receptor tyrosine kinase
D) Nuclear hormone receptor
E) Cytokine receptor
G-protein-coupled receptor
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