New horizons in the pharmacologic management of peptic ulceration

Am J Surg. 1986 Mar;151(3):422-30. doi: 10.1016/0002-9610(86)90483-6.

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.

Publication types

  • Review

MeSH terms

  • Acetylcholine / physiology
  • Benzimidazoles / therapeutic use
  • Chemical Phenomena
  • Chemistry
  • Cimetidine / administration & dosage
  • Cimetidine / therapeutic use
  • Disease Susceptibility
  • Dose-Response Relationship, Drug
  • Duodenal Ulcer / drug therapy
  • Gastric Acid / metabolism
  • Gastric Mucosa / metabolism
  • Gastrins / physiology
  • Histamine / physiology
  • Histamine H2 Antagonists / therapeutic use*
  • Humans
  • Imidazoles / administration & dosage
  • Imidazoles / therapeutic use
  • Intestinal Mucosa / metabolism
  • Peptic Ulcer / drug therapy*
  • Ranitidine / administration & dosage
  • Ranitidine / therapeutic use
  • Receptors, Muscarinic / drug effects
  • Stimulation, Chemical
  • Stomach Ulcer / drug therapy

Substances

  • Benzimidazoles
  • Gastrins
  • Histamine H2 Antagonists
  • Imidazoles
  • Receptors, Muscarinic
  • Cimetidine
  • Histamine
  • Ranitidine
  • etintidine
  • Acetylcholine