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Pharmacotherapy for acid/peptic disorders.

In the 1970s, the identification of the histamine H2-receptor by Black and the subsequent development of histamine H2-receptor antagonists revolutionized our understanding and treatment of acid/peptic disorders. More recently, the identification of hydrogen-potassium-stimulated adenosine triphosphat...

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Detalles Bibliográficos
Autor principal: Schubert, M. L.
Formato: Texto
Lenguaje:English
Publicado: Yale Journal of Biology and Medicine 1996
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2588982/
https://www.ncbi.nlm.nih.gov/pubmed/9112751
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author Schubert, M. L.
author_facet Schubert, M. L.
author_sort Schubert, M. L.
collection PubMed
description In the 1970s, the identification of the histamine H2-receptor by Black and the subsequent development of histamine H2-receptor antagonists revolutionized our understanding and treatment of acid/peptic disorders. More recently, the identification of hydrogen-potassium-stimulated adenosine triphosphatase (H+/K(+)-ATPase) as the proton pump of the parietal cell and the recognition of the prominent role of Helicobacter pylori in the pathogenesis of duodenal and gastric ulceration have heralded a new revolution in our understanding and treatment of these disorders. Substituted benzimidazole compounds (omeprazole, lansoprazole and pantoprazole) that covalently bind to and inactivate the proton pump allow complete and prolonged inhibition of acid secretion. Not only can peptic ulcers now be healed more rapidly with proton pump inhibitors, but refractory ulcers have all but disappeared. Eradication of H. pylori with antibiotics offers, for the first time, a permanent cure for most duodenal and many gastric ulcers.
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spelling pubmed-25889822008-12-01 Pharmacotherapy for acid/peptic disorders. Schubert, M. L. Yale J Biol Med Research Article In the 1970s, the identification of the histamine H2-receptor by Black and the subsequent development of histamine H2-receptor antagonists revolutionized our understanding and treatment of acid/peptic disorders. More recently, the identification of hydrogen-potassium-stimulated adenosine triphosphatase (H+/K(+)-ATPase) as the proton pump of the parietal cell and the recognition of the prominent role of Helicobacter pylori in the pathogenesis of duodenal and gastric ulceration have heralded a new revolution in our understanding and treatment of these disorders. Substituted benzimidazole compounds (omeprazole, lansoprazole and pantoprazole) that covalently bind to and inactivate the proton pump allow complete and prolonged inhibition of acid secretion. Not only can peptic ulcers now be healed more rapidly with proton pump inhibitors, but refractory ulcers have all but disappeared. Eradication of H. pylori with antibiotics offers, for the first time, a permanent cure for most duodenal and many gastric ulcers. Yale Journal of Biology and Medicine 1996 /pmc/articles/PMC2588982/ /pubmed/9112751 Text en
spellingShingle Research Article
Schubert, M. L.
Pharmacotherapy for acid/peptic disorders.
title Pharmacotherapy for acid/peptic disorders.
title_full Pharmacotherapy for acid/peptic disorders.
title_fullStr Pharmacotherapy for acid/peptic disorders.
title_full_unstemmed Pharmacotherapy for acid/peptic disorders.
title_short Pharmacotherapy for acid/peptic disorders.
title_sort pharmacotherapy for acid/peptic disorders.
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2588982/
https://www.ncbi.nlm.nih.gov/pubmed/9112751
work_keys_str_mv AT schubertml pharmacotherapyforacidpepticdisorders