- H2 antagonist
The H2-receptor antagonists (H2RA, often shortened to H2 antagonist) are a class of drugs used to block the action of
histamineon parietal cells in the stomach, decreasing the production of acidby these cells. H2 antagonist are used in the treatment of dyspepsia, although they have largely been surpassed in popularity by the more effective proton pump inhibitors. In the United States, all four FDA-approved members of the group— cimetidine, ranitidine, famotidine, and nizatidine—are available over the counter in relatively low doses.
The prototypical H2 antagonist was cimetidine, developed by Smith, Kline & French (now
GlaxoSmithKline) in the mid-to-late 1960s and first marketed in 1976; sold under the trade name Tagamet, cimetidine would later become the first ever blockbuster drug. The use of quantitative structure-activity relationships (QSAR) led to the development of other agents—starting with ranitidine, first sold as Zantac—which had fewer adverse effects and drug interactions and were more potent.
History and development
Cimetidinewas the prototypical histamine H2-receptor antagonist from which the later members of the class were developed. Cimetidine was the culmination of a project at Smith, Kline & French (SK&F; now GlaxoSmithKline) to develop a histamine receptorantagonist that would suppress stomach acid secretion.
In 1964 it was known that
histaminewas able to stimulate the secretion of stomach acid, but also that traditional antihistamines had no effect on acid production. From these facts the SK&F scientists postulated the existence of two histamine receptors. They designated the one acted on by the traditional antihistamines H1, and the one acted on by histamine to stimulate the secretion of stomach acid H2.
The SK&F team used a
rational drug designprocess starting from the structure of histamine. Hundreds of modified compounds were synthesised in an effort to develop a model of the then-unknown H2 receptor. The first breakthrough was "Nα"-guanylhistamine, a partial H2-receptor antagonist. From this lead the receptor model was further refined and eventually led to the development of burimamide, a specific competitive antagonistat the H2 receptor 100-times more potent than "Nα"-guanylhistamine, proving the existence of the H2 receptor.
Burimamide was still insufficiently potent for oral administration and further modification of the structure, based on modifying the
pKaof the compound, led to the development of metiamide. Metiamide was an effective agent; however, it was associated with unacceptable nephrotoxicityand agranulocytosis. It was proposed that the toxicity arose from the thioureagroup, and similar guanidineanalogues were investigated until the discovery of cimetidine, which would become the first clinically successful H2 antagonist. Ranitidine(common brand name Zantac) was developed by Glaxo (also now GlaxoSmithKline) in an effort to match the success of Smith, Kline & French with cimetidine. Ranitidine was also the result of a rational drug design process utilising the by-then-fairly-refined model of the histamine H2 receptor and quantitative structure-activity relationships ( QSAR).
Glaxo refined the model further by replacing the
imidazole-ring of cimetidine with a furan-ring with a nitrogen-containing substituent, and in doing so developed ranitidine. Ranitidine was found to have a far-improved tolerability profile (i.e. fewer adverse drug reactions), longer-lasting action, and ten times the activity of cimetidine.
Ranitidine was introduced in 1981 and was the world's biggest-selling prescription drug by 1988. The H2-receptor antagonists have since largely been superseded by the even more effective
proton pump inhibitors, with omeprazolebecoming the biggest-selling drug for many years.
The H2 antagonists are competitive antagonists of
histamineat the parietal cellH2 receptor. They suppress the normal secretion of acid by parietal cells and the meal-stimulated secretion of acid. They accomplish this by two mechanisms: histamine released by ECL cells in the stomach is blocked from binding on parietal cell H2 receptors which stimulate acid secretion, and other substances that promote acid secretion (such as gastrinand acetylcholine) have a reduced effect on parietal cells when the H2 receptors are blocked.
Like the H1-antihistamines, the H2 antagonists are
inverse agonists rather than true receptor antagonists.
H2-antagonists are clinically used in the treatment of acid-related
Gastrointestinalconditions. Specifically, these indications may include:Rossi S (Ed.) (2005). Australian Medicines Handbook2005. Adelaide: Australian Medicines Handbook. ISBN 0-9578521-9-3]
Peptic ulcerdisease (PUD)
Gastroesophageal reflux disease(GERD/GORD)
stress ulcer(a specific indication of ranitidine)
People that suffer from heartburn infrequently may take either
antacidsor H2-receptor antagonists for treatment. The H2-antagonists offer several advantages over antacids, including longer duration of action (6–10 hours vs 1–2 hours for antacids), greater efficacy, and ability to be used prophylactically before meals to reduce the chance of heartburn occurring. Proton pump inhibitors, however, are the preferred treatment for erosive esophagitissince they have been shown to promote healing better than H2-antagonists.
Some studies suggest that H2-antagonists might be effective in treating
herpes viruses, such as shinglesand herpes simplex[http://www.lef.org/magazine/mag2001/mar2001_report_tagamet_1.html] .
The H2 antagonists are generally well-tolerated, except for
cimetidinewhere all of the following adverse drug reactions (ADRs) are "common". Infrequent ADRs include hypotension. Rare ADRs include: headache, tiredness, dizziness, confusion, diarrhea, constipation, and rash. Additionally, cimetidine may also cause gynecomastiain males, loss of libido, and impotence, which are reversible upon discontinuation.
longitudinal studyof elderly African Americans published in 2007, long-term use of H2 blockers appeared to increase the risk of cognitive decline. [cite journal |author=Boustani M, Hall KS, Lane KA, "et al" |title=The association between cognition and histamine-2 receptor antagonists in African Americans |journal=J Am Geriatr Soc |volume=55 |issue=8 |pages=1248–53 |year=2007 |month=August |pmid=17661965 |doi=10.1111/j.1532-5415.2007.01270.x |laysummary=http://www.webmd.com/alzheimers/news/20070803/acid-blockers-linked-to-mental-decline |laysource= WebMD|laydate=2007-08-03]
With regard to
pharmacokinetics, cimetidine in particular interferes with some of the body's mechanisms of drug metabolismand elimination through the liver cytochrome P450pathway. Specifically, cimetidine is an inhibitor of the P450 enzymes CYP1A2, CYP2C9, CYP2C19, CYP2D6, CYP2E1, and CYP3A4. By reducing the metabolism of drugs through these enzymes, cimetidine may increase their serum concentrations to toxiclevels. Many drugs are affected, including warfarin, theophylline, phenytoin, lidocaine, quinidine, propranolol, labetalol, metoprolol, tricyclic antidepressants, some benzodiazepines, dihydropyridine calcium channel blockers, sulfonylureas, metronidazole,cite journal |author=Humphries TJ, Merritt GJ |title=Review article: drug interactions with agents used to treat acid-related diseases |journal=Aliment. Pharmacol. Ther. |volume=13 Suppl 3 |issue= |pages=18–26 |year=1999 |month=August |pmid=10491725 |doi=10.1046/j.1365-2036.1999.00021.x |url=http://www3.interscience.wiley.com/cgi-bin/fulltext/119090200] and some recreational drugs such as ethanoland MDMA.
The more recently developed H2-receptor antagonists are less likely to alter CYP metabolism.
Ranitidineis not as potent a CYP inhibitor as cimetidine, although it still shares several of the latter's interactions (such as with warfarin, theophylline, phenytoin, metoprolol, and midazolam). [cite journal |author=Kirch W, Hoensch H, Janisch HD |title=Interactions and non-interactions with ranitidine |journal=Clin Pharmacokinet |volume=9 |issue=6 |pages=493–510 |year=1984 |pmid=6096071] Famotidinehas negligible effect on the CYP system, and appears to have no significant interactions.
* Katzung, Bertram G. (2004). Basic and Clinical Pharmacology, 9th ed. ISBN 0-07-141092-9
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