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dc.contributor.authorCan, Güray
dc.contributor.authorAyvaz, Süleyrnan
dc.contributor.authorCan, Hatice
dc.contributor.authorKaraboğa, İhsan
dc.contributor.authorYılmaz, Bülent
dc.contributor.authorKurt, Mevlüt
dc.contributor.authorKaraca, Turan
dc.contributor.authorAkşit, Hasan
dc.date.accessioned2019-10-10T08:19:31Z
dc.date.available2019-10-10T08:19:31Z
dc.date.issued2016en_US
dc.identifier.issn2210-7401
dc.identifier.issn2210-741X
dc.identifier.urihttps://doi.org/ 10.1016/j.clinre.2015.12.006
dc.identifier.urihttps://hdl.handle.net/20.500.12462/6780
dc.descriptionAkşit, Hasan (Balikesir Author)en_US
dc.description.abstractBackground and objective: Ulcerative colitis is an inflammatory condition of the colon in the gastrointestinal system. Currently, the most potent medications used for ulcerative colitis produce no response in 20-30% of cases. There is a need for more efficient and reliable medications. Tyrosine kinase inhibitors have shown efficacy in some inflammatory diseases. Although dasatinib, a tyrosine kinase inhibitor, suppresses proinflammatory cytokines in colonic tissue, there are a few cases of hemorrhagic colitis with dasatinib. There is no study investigating the effect of dasatinib on experimental colitis. We aimed to investigate the effect of dasatinib in a colitis model induced with acetic acid in our study.Methods: In the study, 24 male Sprague-Dawley rats randomly distributed into 4 groups of 6 rats each as control, dasatinib, colitis and dasatinib + colitis groups. For colitis induction, 4% acetic acid was used. Sacrificing of the rats was performed on the seventh day. Disease activity, morphologic and histological injury, superoxide dismutase, myeloperoxidase and malondialdehyde activity, TNF alpha and CD3 expression were assessed in colonic tissue. Results: Apart from malondialdehyde, significant difference in all parameters between the control and colitis groups was determined. Difference between the colitis and colitis + dasatinib groups was not significant in only weight loss and biochemical parameters. Though dasatinib does not fully resolve the changes in colitis, there was significant regression. Conclusions: Dasatinib decreased the inflammation in a rodent model of colitis. It may be provide this effect by the suppression of TNF alpha. Dasatinib may be one of the treatment options for ulcerative colitis.en_US
dc.language.isoengen_US
dc.publisherElsevier Massonen_US
dc.relation.isversionof10.1016/j.clinre.2015.12.006en_US
dc.rightsinfo:eu-repo/semantics/embargoedAccessen_US
dc.subjectInflammatory-Bowel-Diseaseen_US
dc.subjectChronic Myeloid-Leukemiaen_US
dc.subjectDextran Sulfate Sodiumen_US
dc.subjectTumor-Necrosis-Factoren_US
dc.subjectUlcerative-Colitisen_US
dc.subjectCrohns-Diseaseen_US
dc.subjectRat Modelen_US
dc.subjectPatıenten_US
dc.subjectRemissionen_US
dc.subjectMoleculeen_US
dc.titleThe efficacy of tyrosine kinase inhibitor dasatinib on colonic mucosal damage in murine model of colitisen_US
dc.typearticleen_US
dc.relation.journalClinics and Research in Hepatology and Gastroenterologyen_US
dc.contributor.departmentVeteriner Fakültesien_US
dc.contributor.authorID0000-0002-2500-7781en_US
dc.contributor.authorID0000-0001-5430-9917en_US
dc.identifier.volume40en_US
dc.identifier.issue4en_US
dc.identifier.startpage504en_US
dc.identifier.endpage516en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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