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dc.contributor.authorColak, Mustafa
dc.contributor.authorKalemci, Serdar
dc.contributor.authorAlpaydin, Aylin Ozgen
dc.contributor.authorKaracam, Volkan
dc.contributor.authorMeteoglu, Ibrahim
dc.contributor.authorYilmaz, Osman
dc.contributor.authorItil, Bahriye Oya
dc.date.accessioned2020-11-20T14:40:04Z
dc.date.available2020-11-20T14:40:04Z
dc.date.issued2020
dc.identifier.issn1731-5530
dc.identifier.issn1897-4252
dc.identifier.urihttps://doi.org/10.5114/kitp.2020.97259
dc.identifier.urihttps://hdl.handle.net/20.500.12809/655
dc.descriptionWOS: 000552065400004en_US
dc.descriptionPubMed ID: 32728367en_US
dc.description.abstractIntroduction: Acute lung injury (ALI) and acute respiratory distress syndrome (ARDS) are acute onset syndromes affecting the lungs, which develop for several reasons and are characterized by hypoxemia and diffuse lung infiltration. The activity of thymoquinone (TO) is known in acute lung injury. It is considered that it could be effective in ALI/ARDS treatment by ensuring possible COX-2 inhibition. Aim: By this study was to show the protective activity of TO in lipopolysaccharide (LPS) induced acute lung injury. Material and methods: A total of 28 BALB/c male mice were randomized to 4 groups of 7 as the Control group, TO group (3 mg/kg), LPS group (5 mg/kg) and TQ treatment group. TQ was administered intraperitoneally 1 hour before the intratracheal administration of LPS (5 mg/kg). The mice were sacrificed 6 hours after the LPS administration and the lungs were extracted for histopathological examination. All experimental procedures complied with the requirements of the Animal Care and Ethics Committee of Dokuz Eylul University. Results: When all the study groups were compared, significant differences were found between the groups in terms of the degrees of neutrophil migration (p = 0.042), intra-alveolar hemorrhage (p = 0.004) and alveolar destruction (p < 0.0006). A significant recovery was observed in the lung histopathological changes (neutrophil migration, intra-alveolar hemorrhage and alveolar destruction) in the TO treatment group. Conclusions: The results of this study showed that TO may have a protective effect against LPS-induced acute lung injury. The possible mechanism could be considered to be cyclooxy-genase 2 (COX-2) inhibition.en_US
dc.item-language.isoengen_US
dc.publisherTermedia Publishing House Ltden_US
dc.item-rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectAcute Lung Injuryen_US
dc.subjectThymoquinoneen_US
dc.subjectLipopolysaccharideen_US
dc.titleEfficacy of thymoquinone in the treatment of experimental lipopolysaccharide-induced acute lung injuryen_US
dc.item-typearticleen_US
dc.contributor.departmenten_US
dc.contributor.departmentTemp[Colak, Mustafa; Alpaydin, Aylin Ozgen; Itil, Bahriye Oya] Dokuz Eylul Univ, Chest Dis Dept, Izmir, Turkey -- [Kalemci, Serdar] Mugla Sitki Kocman Univ, Chest Dis Dept, Mugla, Turkey -- [Karacam, Volkan] Dokuz Eylul Univ, Chest Surg Dept, Izmir, Turkey -- [Meteoglu, Ibrahim] Adnan Menderese Univ, Pathol Dept, Aydin, Turkey -- [Yilmaz, Osman] Dokuz Eylul Univ, Lab Anim Sci, Izmir, Turkeyen_US
dc.identifier.doi10.5114/kitp.2020.97259
dc.identifier.volume17en_US
dc.identifier.issue2en_US
dc.identifier.startpage65en_US
dc.identifier.endpage69en_US
dc.relation.journalKardiochirurgia I Torakochirurgia Polska-Polish Journal of Thoracic and Cardiovascular Surgeryen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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