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Combination of allopurinol and hyperbaric oxygen therapy

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dc.contributor.author Cömert, Bilgin
dc.contributor.author Işık, Ahmet Turan
dc.contributor.author Aydın, Sezai
dc.contributor.author Bozoğlu, Ergun
dc.contributor.author Ünal, Bülent
dc.contributor.author Deveci, Salih
dc.contributor.author Mas, Nuket
dc.contributor.author Çınar, Eşref
dc.contributor.author Mas, Mehmet Refik
dc.date.accessioned 2017-08-14T10:20:16Z
dc.date.available 2017-08-14T10:20:16Z
dc.date.issued 2008
dc.identifier.citation Cömert, B. Işık, A. T. Aydın, S. Bozoğlu, E. Ünal, B. Deveci, S. Mas, N. Çınar, E. Mas, M. R. (2008). Combination of allopurinol and hyperbaric oxygen therapy. Pancreas. 13(46): 6203-6207. tr_TR
dc.identifier.issn 0885-3177
dc.identifier.uri http://content.wkhealth.com/linkback/openurl?sid=WKPTLP:landingpage&an=00006676-200811000-00048
dc.identifier.uri http://hdl.handle.net/11616/7557
dc.description.abstract AIM: To investigate the individual and combined effects of allopurinol and hyperbaric oxygen (HBO) therapy on biochemical and histopathological changes, oxidative stress, and bacterial translocation (BT) in the experimental rat acute pancreatitis (AP). METHODS: Eighty-five Sprague-Dawley rats were included in the study. Fifteen of the eighty-five rats were used as controls (sham, GroupⅠ). AP was induced via intraductal taurocholate infusion in the remaining seventy rats. Rats that survived to induction of acute necrotizing pancreatitis were randomized into four groups. Group Ⅱ received saline, Group Ⅲ allopurinol, Group Ⅳ allopurinol plus HBO and Group Ⅴ HBO alone. Serum amylase levels, oxidative stress parameters, BT and histopathologic scores were determined. RESULTS: Serum amylase levels were lower in Groups Ⅲ, Ⅳ and Ⅴ compared to Group Ⅱ (974 ± 110, 384 ± 40, 851 ± 56, and 1664 ± 234 U/L, respectively, P < 0.05, for all). Combining the two treatment optionsrevealed significantly lower median [25-75 percentiles] histopathological scores when compared to individual administrations (13 [12.5-15] in allopurinol group, 9.5 [7-11.75] in HBO group, and 6 [4.5-7.5] in combined group, P < 0.01). Oxidative stress markers were significantly better in all treatment groups compared to the controls. Bacterial translocation into the pancreas and mesenteric lymph nodes was lower in Groups Ⅲ, Ⅳ and Ⅴ compared to Group Ⅱ (54%, 23%, 50% vs 100% for translocation to pancreas, and 62%, 46%, 58% vs 100% for translocation to mesenteric lymph nodes, respectively, P < 0.05 for all). CONCLUSION: The present study confirms the benefit of HBO and allopurinol treatment when administered separately in experimental rat AP. Combination of these treatment options appears to prevent progression of pancreatic injury parameters more effectively. tr_TR
dc.language.iso eng tr_TR
dc.publisher Pancreas tr_TR
dc.relation.isversionof 10.1097/01.MPA.0000335435.47969.20 tr_TR
dc.rights info:eu-repo/semantics/openAccess tr_TR
dc.subject Experimental pancreatitis tr_TR
dc.subject Allopurinol tr_TR
dc.subject Hyperbaric oxygen tr_TR
dc.title Combination of allopurinol and hyperbaric oxygen therapy tr_TR
dc.type article tr_TR
dc.relation.journal Pancreas tr_TR
dc.contributor.department İnönü Üniversitesi tr_TR
dc.contributor.authorID 116537 tr_TR
dc.identifier.volume 13 tr_TR
dc.identifier.issue 46 tr_TR
dc.identifier.startpage 6203 tr_TR
dc.identifier.endpage 6207 tr_TR


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