Pharmacology for Anaesthesia and Intensive Care

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19 Drugs acting on the gut

activation. Gastrin and ACh also stimulate the adjacent paracrine cells to produce
and release histamine, which acts on the parietal cell, increasing cAMP and therefore
acid secretion.

H 2 receptor antagonists
Cimetidine
Cimetidine is the only H 2 receptor antagonist with an imidazole structure.

Uses
Itis used in peptic ulcer disease, reflux oesophagitis, Zollinger–Ellison syndrome and
pre-operatively in those at risk of aspiration. It has not been shown to be of benefit in
active haematemesis, although it does have a prophylactic role in those with critical
illness.

Mechanism of action
Cimetidine is a competitive and specific antagonist of H 2 receptors at parietal cells.

Effects
Gut–the gastric pH is raised and the volume of secretions reduced, while there is
no change in gastric emptying time or lower oesophageal sphincter tone.
Cardiovascular – bradycardia and hypotension follow rapid intravenous adminis-
tration.
Central nervous system – confusion, hallucinations and seizures are usually only
seen when impaired renal function leads to high plasma levels.
Respiratory system – low-grade aspiration of gastric content that has been stripped
of its acidic, antibacterial environment will result in increased nosocomial pul-
monary infections in critically ill ventilated patients.
Endocrine – gynaecomastia, impotence and a fall in sperm count is seen in men
due to its anti-androgenic effects.
Metabolic – it inhibits hepatic cytochrome P450 and will slow the metabolism of
the following drugs: lidocaine, propranolol, diazepam, phenytoin, tricyclic antide-
pressants, warfarin and aminophylline.

Kinetics
Cimetidine is well absorbed from the small bowel (oral bioavailability approximately
60%), poorly plasma protein bound (20%), partially metabolized (up to 60% if admin-
istered orally) in the liver by cytochrome P450 and approximately 50% excreted
unchanged in the urine.

Ranitidine
Ranitidine is more potent than cimetidine.
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