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dc.contributor.authorCan, Güray
dc.contributor.authorAyvaz, Süleyman
dc.contributor.authorCan, Hatice
dc.contributor.authorDemirtaş, Selim
dc.contributor.authorAkşit, Hasan
dc.contributor.authorYılmaz, Bülent
dc.contributor.authorKorkmaz, Uğur
dc.contributor.authorKurt, Mevlüt
dc.contributor.authorKaraca, Turanen_US
dc.date.accessioned2019-10-17T07:08:06Z
dc.date.available2019-10-17T07:08:06Z
dc.date.issued2015en_US
dc.identifier.issn1873-9946
dc.identifier.issn1876-4479
dc.identifier.urihttps://doi.org/10.1093/ecco-jcc/jjv114
dc.identifier.urihttps://hdl.handle.net/20.500.12462/7498
dc.descriptionAkşit, Hasan (Balikesir Author)en_US
dc.description.abstractBackground and aims: Inflammatory bowel disease is a chronic inflammatory disease of the gastrointestinal system. In some cases, current medications used for inflammatory bowel disease may not be enough for remission, creating a need for more potent and reliable medications. There is no study showing the efficacy of fostamatinib, with proven effects on some inflammatory diseases, on ulcerative colitis. In our study we planned to research the efficacy of fostamatinib, a spleen tyrosine kinase inhibitor, on acetic acid-induced colitis. Methods: The study included 28 male Sprague-Dawley rats, randomly divided into control group, fostamatinib group, colitis group and fostamatinib + colitis group, each containing seven rats. Colitis induction was performed with 4% acetic acid. Colonic inflammation was assessed with disease activity index, macroscopic and histological damage scores, colonic myeloperoxidase, malondialdehyde and superoxide dismutase activity, and tumour necrosis factor alpha [TNF alpha], CD3, Syk, and phospho-Syk expression. Results: There was a significant difference between the colitis and control groups in terms of all parameters. The disease activity index, macroscopic and microscopic damage scores, immunohistochemical TNF alpha, CD3, Syk, and phospho-Syk expression, and tissue myeloperoxidase activity were found to be significantly lower in the colitis + fostamatinib group compared with the colitis group. There was no significant difference between the two groups in terms of myeloperoxidase and malondialdehyde activity. Conclusions: Fostamatinib reduced the inflammatory damage in the experimental colitis. This effect may be due to suppression of TNF alpha, T-lymphocytes, and neutrophils in colonic mucosa via suppression of Syk. Fostamatinib may be an appropriate treatment alternative for ulcerative colitis. Further clinical studies are required to support this.en_US
dc.language.isoengen_US
dc.publisherOxford Univ Pressen_US
dc.relation.isversionof10.1093/ecco-jcc/jjv114en_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectAcetic Acid-Induced Colitisen_US
dc.subjectFostamatiniben_US
dc.subjectRatsen_US
dc.subjectSpleen Tyrosine Tinaseen_US
dc.titleThe syk inhibitor fostamatinib decreases the severity of colonic mucosal damage in a rodent model of colitisen_US
dc.typearticleen_US
dc.relation.journalJournal of Crohns & Colitisen_US
dc.contributor.departmentVeteriner Fakültesien_US
dc.contributor.authorID0000-0002-2500-7781en_US
dc.contributor.authorID0000-0003-3726-5945en_US
dc.contributor.authorID0000-0002-6054-9244en_US
dc.contributor.authorID0000-0001-5430-9917en_US
dc.identifier.volume9en_US
dc.identifier.issue10en_US
dc.identifier.startpage907en_US
dc.identifier.endpage917en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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