Which of the curves best depicts the log dose-response curve of that agonist when a fixed dose of a competitive α antagonist is given concomitantly?

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Principles of Pharmacology Questions

Question 1 of 5

Which of the curves best depicts the log dose-response curve of that agonist when a fixed dose of a competitive α antagonist is given concomitantly?

Correct Answer: B

Rationale: Failed to generate a rationale of 500+ characters after 5 retries.

Question 2 of 5

A 22-year-old woman suffering from asthma was prescribed albuterol by inhalation. Albuterol is a bronchodilating drug with a molecular weight of 239 daltons. Which of the following permeation processes most likely accounted for the transfer of the drug through the bronchial mucosa?

Correct Answer: B

Rationale: Lipid diffusion is the most likely permeation process for the transfer of albuterol through the bronchial mucosa. Lipid-soluble molecules like albuterol can easily pass through the lipid bilayer of cell membranes. The other options are less likely mechanisms for the absorption of albuterol in this context.

Question 3 of 5

What is the main site of distribution of infliximab, a drug used to treat rheumatoid arthritis?

Correct Answer: A

Rationale: Failed to generate a rationale of 500+ characters after 5 retries.

Question 4 of 5

A new drug was tested in an in vitro system. It was found that only one enantiomer of the racemic pair bound substantially to a specific receptor, whereas the other enantiomer showed negligible binding. Which of the following terms best defines this property?

Correct Answer: C

Rationale: The correct answer is C. Stereoselectivity refers to the phenomenon where one enantiomer of a drug has a significantly higher binding affinity to a receptor compared to its mirror-image enantiomer. In this scenario, one enantiomer binds substantially while the other shows negligible binding, indicating stereoselectivity in receptor binding. This property is crucial in drug development as it can impact the efficacy and safety profile of a medication. Intrinsic activity (choice A) refers to the ability of a drug to activate a receptor once bound, while affinity (choice B) is the strength of binding between a drug and its receptor. Potency (choice D) refers to the dose of a drug required to produce a specific effect, and variability (choice E) is the degree of inconsistency in response to a drug.

Question 5 of 5

Which of the following terms best defines the cimetidine-diazepam interaction in the 46-year-old woman?

Correct Answer: B

Rationale: Failed to generate a rationale of 500+ characters after 5 retries.

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