Last updated on June 21, 2019 at 15:37
Introduction to vomiting
Vomiting is a defensive response intended to rid the body of toxic or irritating material. It’s regulating by a vomiting centre, comprised of the reticular formation and the area postrema/chemosensitive trigger zone in the fourth ventricle.
Many receptors are involved in stimulating vomiting, including:
- Histamine H1 receptor
- Dopamine D2 receptor
- Muscarinic receptor
- Serotonin 5-HT3 receptor
- Neurokinin NK1 receptor
The chemoreceptor trigger zone expresses D2 and 5-HT3 receptors.
Sometimes it can be clinically useful to induce vomiting. This is most notably useful if someone has ingested something poisonous. For this emetine and apomorphine can be used. Apomorphine is a dopamine receptor agonist.
Antiemetics are more important clinically than emetics. Many receptors are involved in vomiting, so many different drugs with different mechanisms of actions have antiemetic effect.
The important drugs here are:
- 1st generation histamine H1 receptor antagonists
- Dopamine D2 receptor antagonists
- Muscarinic receptor antagonists
- Serotonin 5-HT3 receptor antagonists
- Neurokinin NK1 receptors antagonists
Antihistamines and scopolamine are particularly affective in nausea caused by motion sickness.
D2 antagonists, 5-HT3 antagonists, corticosteroids, cannabinoids and NK1 antagonists are particularly effective in nausea caused by chemotherapy or radiotherapy. Often two or more drugs from these classes are combined to give stronger antiemetic effect.
Most cytotoxic drugs induce nausea and vomiting, especially cisplatin, cyclophosphamide and doxorubicin.
Mechanism of action:
The drugs act on their respective receptors.
Scopolamine is often administered as a transdermal patch.
The D2 antagonists can give extrapyramidal symptoms. Serotonin antagonists can give headache.
These drugs increase the gastrointestinal motility. This can be useful in GERD, gastrointestinal hypomotility, decreased gastric emptying or obstipation.
Three drugs are important here; domperidone, metoclopramide and prucalopride.
Domperidone and metoclopramide are used in GERD and disorders of gastric emptying.
Prucalopride is used as a laxative when other laxative treatments have failed.
Mechanism of action:
Domperidone is a dopamine D2 receptor antagonist.
Metoclopramide is D2 receptor antagonist and a serotonin 5-HT4 receptor agonist.
Prucalopride is a serotonin 5-HT4 receptor agonist.
Blocking D2 receptors increases the tone of the lower oesophageal sphincter. Activating 5-HT4 receptors stimulate gastric emptying and duodenal peristalsis.
31. Drugs used in the treatment of peptic ulcer
33. Laxatives, antidiarrhoeal agents, drug treatment of inflammatory bowel disease and paralytic ileus, digestives, drugs used in cholelithiasis