Abstract
Greatly improved understanding of the cellular basis for gastric acid secretion and gastroduodenal mucosal defense has led to a dramatic improvement in the pharmacologic treatment of peptic ulcer disease. The advances produced by cimetidine and ranitidine are being continued by a new generation of histamine receptor antagonists, as well as by other anti-ulcer agents. These new drugs, when used appropriately, will greatly expand the surgeon's ability to treat patients with peptic ulcer disease. A knowledge of the pathophysiologic characteristics of peptic ulceration and of the inherent limitations of each agent will become increasingly important for surgeons who treat these patients.
MeSH terms
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Acetylcholine / physiology
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Benzimidazoles / therapeutic use
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Chemical Phenomena
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Chemistry
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Cimetidine / administration & dosage
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Cimetidine / therapeutic use
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Disease Susceptibility
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Dose-Response Relationship, Drug
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Duodenal Ulcer / drug therapy
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Gastric Acid / metabolism
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Gastric Mucosa / metabolism
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Gastrins / physiology
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Histamine / physiology
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Histamine H2 Antagonists / therapeutic use*
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Humans
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Imidazoles / administration & dosage
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Imidazoles / therapeutic use
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Intestinal Mucosa / metabolism
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Peptic Ulcer / drug therapy*
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Ranitidine / administration & dosage
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Ranitidine / therapeutic use
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Receptors, Muscarinic / drug effects
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Stimulation, Chemical
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Stomach Ulcer / drug therapy
Substances
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Benzimidazoles
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Gastrins
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Histamine H2 Antagonists
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Imidazoles
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Receptors, Muscarinic
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Cimetidine
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Histamine
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Ranitidine
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etintidine
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Acetylcholine