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  5. Άρθρα σε επιστημονικά περιοδικά ( Ανοικτά) - ΙΑΤ
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Please use this identifier to cite or link to this item: https://olympias.lib.uoi.gr/jspui/handle/123456789/18959
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dc.contributor.authorGiannoukas, A. D.en
dc.contributor.authorBaltoyiannis, G.en
dc.contributor.authorMilonakis, M.en
dc.contributor.authorNastos, D.en
dc.contributor.authorPapagikos, L.en
dc.contributor.authorKappas, A. M.en
dc.contributor.authorFatouros, M.en
dc.contributor.authorPapadimitriou, C.en
dc.contributor.authorCassioumis, D.en
dc.date.accessioned2015-11-24T18:55:57Z-
dc.date.available2015-11-24T18:55:57Z-
dc.identifier.issn0364-2313-
dc.identifier.urihttps://olympias.lib.uoi.gr/jspui/handle/123456789/18959-
dc.rightsDefault Licence-
dc.subjectAnimalsen
dc.subjectAnti-Inflammatory Agents, Non-Steroidal/*toxicityen
dc.subjectAnti-Ulcer Agents/*pharmacologyen
dc.subjectCombined Modality Therapyen
dc.subjectDiclofenac/*toxicityen
dc.subjectDogsen
dc.subjectDuodenum/drug effects/pathologyen
dc.subjectFemaleen
dc.subjectGastric Acidity Determinationen
dc.subjectGastric Mucosa/*drug effects/pathologyen
dc.subjectInjections, Intramuscularen
dc.subjectIntestinal Mucosa/*drug effects/pathologyen
dc.subjectMaleen
dc.subjectMisoprostol/*pharmacologyen
dc.subjectPeptic Ulcer/*chemically induced/pathology/prevention & controlen
dc.subjectTreatment Outcomeen
dc.subject*Vagotomy, Proximal Gastricen
dc.titleProtection of the gastroduodenal mucosa from the effects of diclofenac sodium: role of highly selective vagotomy and misoprostolen
heal.typejournalArticle-
heal.type.enJournal articleen
heal.type.elΆρθρο Περιοδικούel
heal.identifier.secondaryhttp://www.ncbi.nlm.nih.gov/pubmed/8662142-
heal.languageen-
heal.accesscampus-
heal.recordProviderΠανεπιστήμιο Ιωαννίνων. Σχολή Επιστημών Υγείας. Τμήμα Ιατρικήςel
heal.publicationDate1996-
heal.abstractThe aim of this study was to determine the effectiveness of highly selective vagotomy (HSV) or misoprostol, a prostaglandin E1 (PGE1) analog, for protecting the gastroduodenal mucosa (GDM) from the effects of diclofenac sodium (DS). Fifty mongrel dogs were randomly allocated to five groups. HSV alone was performed in group I dogs (controls) to standardize the operation. DS was given intramuscularly for 12 consecutive days to the group II dogs, whereas in the group III dogs HSV was performed, followed a month later by DS administration, as in group II. DS was given in combination with misoprostol for 12 days to the group IV dogs. HSV was performed on the group V dogs, and a month later DS and misoprostol were given, as in group IV. After sacrificing the animals the GDM was examined for macroscopic and histologic lesions. Statistical analysis was made by Fisher's exact test. HSV alone did not protect the gastric or duodenal mucosa from the effects of DS (p = 0.474 and p = 0.62, respectively). Misoprostol alone also did not offer significant protection to the gastric or the duodenal mucosa (p = 0.08 and p = 0.65, respectively). The combination of HSV plus misoprostol protected the gastric mucosa (group V, p = 0.007) but not the duodenal mucosa (group V, p = 0.08). Hence HSV or misoprostol alone offers no protection to the GDM from the effects of DS. The combination of HSV and misoprostol offers significant protection only to gastric mucosa. Enhancement of the mucosal defense mechanisms combined with strong reduction of gastric acidity may offer adequate protection to gastric mucosa from the effects of nonsteroidal antiinflammatory drugs.en
heal.journalNameWorld J Surgen
heal.journalTypepeer-reviewed-
heal.fullTextAvailabilityTRUE-
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