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dc.contributor.authorÖzçiçek, Fatih
dc.contributor.authorÇankaya, Murat
dc.contributor.authorÇimen, Ferda K.
dc.contributor.authorKafa, Ayşe H. T.
dc.contributor.authorNalkıran, Hatice Sevim
dc.contributor.authorSüleyman, Bahadır
dc.contributor.authorAltuner, Durdu
dc.contributor.authorÇetin, Nihal
dc.date.accessioned2020-12-19T19:56:02Z
dc.date.available2020-12-19T19:56:02Z
dc.date.issued2016
dc.identifier.citationÖzçiçek, F., Çankaya, M., Çimen, F.K., Kafa, A.H.T., Nalkıran, H.S., Süleyman, B., Altuner, D. & Çetin, N. (2016). Effects of nimesulide on oxidative mucosal injury induced by cisplatin in rat duodenum and jejunum. Latin American Journal of Pharmacy, 35, 1110-1115.en_US
dc.identifier.issn0326-2383
dc.identifier.urihttps://hdl.handle.net/11436/2658
dc.descriptionCetin, Nihal/0000-0003-3233-8009en_US
dc.descriptionWOS: 000383364400005en_US
dc.description.abstractIn this study, the impact of nimesulide on oxidative stress induced by cisplatin in rat duodenum and jejunum tissue was assessed by evaluating the biochemical and histopathological changes. the rats in the study were assigned to three groups: the control group and cisplatin (Cis) group were given distilled water, and the nimesulide + cisplatin (Nim + Cis) group was given nimesulide (50 mg/kg) orally for seven days. the Cis and Nim + Cis groups were injected with a single dose of intraperitoneal cisplatin (6 mg/kg) on the first day. After the rats were euthanized, the duodenum and jejunum of each rat was removed for the assessment of biochemical markers and histopathological evaluation. Cisplatin administration in the Cis group resulted in increased levels of malondialdehyde and nitric oxide and decreased levels of total glutathione, glutathione reductase, and catalase compared to the healthy and Nim + Cis groups. Nimesulide significantly inhibited the increase of oxidants (p < 0.001) and the decrease of antioxidants caused by cisplatin (p < 0.001). Inflammation, damage to the villus epithelium, hemorrhage, and capillary proliferation were determined histopathologically in the Cis group. the results of this study indicate that oxidative stress caused by cisplatin may be preventable by co-administered nimesulide.en_US
dc.language.isoengen_US
dc.publisherColegio Farmaceuticos Provincia de Buenos Airesen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectNimesulideen_US
dc.subjectOxidative stressen_US
dc.subjectRatsen_US
dc.subjectSmall intestineen_US
dc.titleEffects of nimesulide on oxidative mucosal injury induced by cisplatin in rat duodenum and jejunumen_US
dc.typearticleen_US
dc.contributor.departmentRTEÜ, Tıp Fakültesi, Temel Tıp Bilimleri Bölümüen_US
dc.contributor.institutionauthorNalkıran, Hatice Sevim
dc.identifier.volume35en_US
dc.identifier.startpage1110en_US
dc.identifier.endpage1115en_US
dc.relation.journalLatin American Journal of Pharmacyen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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