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Pharmacology · Endocrine drugs: atosiban tocolysis
Sample itemA woman at 30 weeks in preterm labour has severe cardiac disease, so a beta-agonist and nifedipine are avoided. Atosiban is chosen. Atosiban inhibits uterine contractions by antagonising which receptor?
Original practice item, not a recalled exam question. Nothing here is recorded.
The answer and the reasoning
A. Oxytocin receptor
Atosiban is a competitive antagonist of oxytocin receptors (with some vasopressin V1a activity) in the myometrium, reducing contractions with few maternal cardiovascular effects. Beta-2 agonists cause tachycardia and pulmonary oedema, nifedipine blocks calcium channels, and indomethacin inhibits prostaglandin synthesis.
Option by option
A. Oxytocin receptor (correct)
Correct. Atosiban blocks the oxytocin receptor.
B. L-type calcium channel
Calcium channel blockade is the action of nifedipine.
C. Beta-2 adrenergic receptor
Beta-2 receptor stimulation is the action of terbutaline and ritodrine.
D. Cyclo-oxygenase-2 enzyme
Cyclo-oxygenase inhibition is the action of indomethacin.
Source note: Original NextPrep sample item — pending expert review. This item is original practice material awaiting independent expert review, so confirm important facts in a standard textbook.
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