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dc.creatorMirkov, Ivana
dc.creatorPopov Aleksandrov, Aleksandra
dc.creatorDemenesku, Jelena
dc.creatorNinkov, Marina
dc.creatorTucović, Dina
dc.creatorKataranovski, Dragan
dc.creatorKataranovski, Milena
dc.date.accessioned2017-02-17T14:51:36Z
dc.date.available2017-02-17T14:51:36Z
dc.date.issued2017
dc.identifier.issn1556-9527
dc.identifier.issn1556-9527
dc.identifier.urihttps://www.tandfonline.com/doi/full/10.1080/15569527.2016.1275664
dc.identifier.urihttps://radar.ibiss.bg.ac.rs/handle/123456789/2555
dc.description.abstractPurpose: Warfarin (WF) is an anticoagulant which also affects physiological processes other than hemostasis. Our previous investigations showed the effect of WF which gained access to the organism via skin on resting peripheral blood granulocytes. Based on these data, the aim of the present study was to examine whether WF could modulate the inflammatory processes as well. To this aim the effect of WF on the inflammatory response induced by subcutaneous sponge implantation in rats was examined. Materials and methods: Warfarin-soaked polyvinyl sponges (WF-sponges) were implanted subcutaneously and cell infiltration into sponges, the levels of nitric oxide (NO) and inflammatory cytokines tumor necrosis factor (TNF) and interleukin-6 (IL-6) production by sponge cells were measured as parameters of inflammation. T cell infiltration and cytokine interferon-γ (IFN-γ), interleukin-17 (IL-17) and interleukin-10 (IL-10) were measured at day 7 post implantation. Results: Warfarin exerted both stimulatory and suppressive effects depending on the parameter examined. Flow cytometry of cells recovered from sponges showed higher numbers of granulocytes (HIS48+ cells) at days 1 and 3 post implantation and CD11b+ cells at day 1 compared to control sponges. Cells from WF-sponges had an increased NO production (Griess reaction) at days 1 and 7. In contrast, lower levels of TNF (measured by ELISA) production by cells recovered from WF-soaked sponges were found in the early (day one) phase of reaction with unchanged levels at other time points. While IL-6 production by cells recovered from WF-soaked sponges was decreased at day 1, it was increased at day 7. Higher T cell numbers were noted in WF sponges at day 7 post implantation, and recovered cells produced more IFN-γ and IL-17, while IL-10 production remained unchanged. Conclusions: Warfarin affects some of the parameters of inflammatory reaction induced by subcutaneous polyvinyl sponge implantation. Differential (both stimulatory as well as inhibitory) effects of WF on inflammatory response to sponge implants might affect the course and/or duration of this reaction.en
dc.relationinfo:eu-repo/grantAgreement/MESTD/Basic Research (BR or ON)/173039/RS//
dc.rightsrestrictedAccess
dc.sourceCutaneous and Ocular Toxicology
dc.subjectInflammation
dc.subjectRats
dc.subjectSubcutaneous polyvinyl sponge implants
dc.subjectT cells
dc.subjectWarfarin
dc.titleWarfarin affects acute inflammatory response induced by subcutaneous polyvinyl sponge implantation in ratsen
dc.typearticle
dc.rights.licenseARR
dcterms.abstractНинков, Марина; Милеуснић, Дина; Катарановски, Милена; Попов Александров, Александра; Деменеску, Јелена; Мирков, Ивана; Катарановски, Драган
dc.rights.holder© 2017 Informa UK Limited, trading as Taylor & Francis Group
dc.description.otherCutaneous and Ocular Toxicology (2017)
dc.identifier.doi10.1080/15569527.2016.1275664
dc.identifier.pmid28067070
dc.identifier.scopus2-s2.0-85010705047
dc.identifier.wos000404791400012
dc.citation.apaMirkov, I., Popov Aleksandrov, A., Demenesku, J., Ninkov, M., Mileusnic, D., Kataranovski, D., & Kataranovski, M. (2017). Warfarin affects acute inflammatory response induced by subcutaneous polyvinyl sponge implantation in rats. Cutaneous and Ocular Toxicology. "in press"
dc.citation.vancouverMirkov I, Popov Aleksandrov A, Demenesku J, Ninkov M, Mileusnic D, Kataranovski D, Kataranovski M. Warfarin affects acute inflammatory response induced by subcutaneous polyvinyl sponge implantation in rats. Cutan Ocul Toxicol. 2017;DOI:10.1080/15569527.2016.1275664.
dc.type.versionacceptedVersion
dc.citation.rankM23


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