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Antiemetics and Laxatives Quiz
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A 22-year-old woman is planning a long sea voyage and is concerned about developing motion sickness. She is prescribed a transdermal patch containing hyoscine hydrobromide. Which of the following best explains how this drug prevents motion sickness?
- A Blockade of 5-HT3 receptors on vagal afferents in the gut You picked ✕
- B Blockade of dopamine D2 receptors in the chemoreceptor trigger zone You picked ✕
- C Peripheral inhibition of smooth muscle contraction without central effects You picked ✕
- D Blockade of histamine H1 receptors in the vestibular nuclei You picked ✕
- E Blockade of central muscarinic receptors in vestibular pathways involved in vomiting You picked ✓
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The answer is E: Blockade of central muscarinic receptors in vestibular pathways involved in vomiting
Explanation
Why E is correct
See Antimuscarinics. Option E is correct because hyoscine hydrobromide is an antimuscarinic drug that crosses the blood-brain barrier, the tightly sealed lining of the brain's blood vessels, and blocks muscarinic receptors in the vestibular nuclei and the chemoreceptor trigger zone. Motion sickness arises when the vestibular system, the balance organs of the inner ear and the brainstem nuclei that receive their signals, is overstimulated and sends excessive signals to the vomiting centre in the medulla. The dominant receptors on this pathway are muscarinic (M) and histamine H1 receptors, so blocking muscarinic receptors reduces cholinergic (acetylcholine) transmission from the vestibular apparatus and prevents nausea and vomiting. Hyoscine hydrobromide is the standard treatment for motion sickness and is available as tablets or as a transdermal patch, which gives steady release for a long voyage. Its side effects are the typical antimuscarinic ones: dry mouth, blurred vision, urinary retention, constipation, drowsiness and confusion in older people, and it should be avoided in glaucoma and prostatic hyperplasia. A memory aid: hyoscine hydrobromide goes to the brain for travel sickness, whereas hyoscine butylbromide stays in the gut for cramps.
- Drug class: hyoscine hydrobromide is an antimuscarinic that crosses the blood-brain barrier.
- Site of action: it blocks muscarinic receptors in the vestibular nuclei and the chemoreceptor trigger zone.
- Use: standard treatment for motion sickness, as tablets or a transdermal patch.
- Cautions: dry mouth, blurred vision and urinary retention are typical, and avoid it in glaucoma and prostatic hyperplasia.
Why the other options are incorrect
- A. Blockade of 5-HT3 receptors on vagal afferents in the gut: 5-HT3 blockade is the action of ondansetron, which is mainly used for chemotherapy-induced nausea. Hyoscine is not a 5-HT3 antagonist. Your answer
- B. Blockade of dopamine D2 receptors in the chemoreceptor trigger zone: Dopamine D2 blockade is the mechanism of drugs such as metoclopramide. Hyoscine is an antimuscarinic and does not block D2 receptors. Your answer
- C. Peripheral inhibition of smooth muscle contraction without central effects: This describes hyoscine butylbromide, a quaternary derivative that does not cross the blood-brain barrier and is used for visceral cramping. Hyoscine hydrobromide acts in the brain. Your answer
- D. Blockade of histamine H1 receptors in the vestibular nuclei: H1 blockade is the action of antihistamines such as cyclizine and cinnarizine, which also treat motion sickness. Hyoscine is an antimuscarinic and acts on muscarinic receptors, not H1 receptors. Your answer
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1
Which of the following best describes the mechanism of action of bulk-forming laxatives such as ispaghula husk?
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A 22-year-old woman has severe nausea and vomiting 6 hours after starting cisplatin chemotherapy for ovarian cancer. The oncology team prescribes ondansetron. Which receptor does ondansetron mainly antagonise to produce its antiemetic effect?
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