Please use this identifier to cite or link to this item: https://hdl.handle.net/11499/10711
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dc.contributor.authorKamışlı, S.-
dc.contributor.authorÇiftçi, Osman-
dc.contributor.authorTaşlıdere, A.-
dc.contributor.authorBaşak Türkmen, N.-
dc.contributor.authorÖzcan, C.-
dc.date.accessioned2019-08-16T13:32:33Z
dc.date.available2019-08-16T13:32:33Z
dc.date.issued2018-
dc.identifier.issn0892-3973-
dc.identifier.urihttps://hdl.handle.net/11499/10711-
dc.identifier.urihttps://doi.org/10.1080/08923973.2018.1490318-
dc.description.abstractAim: The aim of this study was to investigate the beneficial effects of 18ß-glycyrrhetinic acid (GA) on the experimental allergic encephalomyelitis (EAE) in C57BL/6 mice. GA is a natural substance found in the root of licorice and is used in traditional Chinese medicine. It has many pharmacological activities such as antioxidant, anti-inflammatory, and anti-cancer effects. Materials and methods: A total of 40 C57BL/6 mice were divided equally into four groups: (1) Control, (2) EAE, (3) GA and (4) GA + EAE. 14 days after induction of EAE with MOG35-55 and pertussis toxin, mice were treated with GA at doses of 100 mg/kg/day for 7 days intraperitoneally. Results: To our results, oxidative stress and lipid peroxidations (elevated TBARS levels, decreased GPx, SOD, CAT, and GSH levels) were significantly (p <.01) increased, causing EAE in brain tissue. Also, histopathological damage (Caspase-3 and IL-17 activity, p ?.01) and cytokine levels (TNF-? and IL-1ß, p <.01) were induced with EAE in mice brain tissue. On the other hand, GA treatment significantly (p <.01) reversed oxidative histological and immunological alterations caused by EAE. Conclusions: In conclusion, the GA treatment can protect the brain tissue against EAE in mice with its antioxidant and anti-inflammatory properties. © 2018, © 2018 Informa UK Limited, trading as Taylor & Francis Group.en_US
dc.language.isoenen_US
dc.publisherTaylor and Francis Ltden_US
dc.relation.ispartofImmunopharmacology and Immunotoxicologyen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subject18ß-glycyrrhetinic aciden_US
dc.subjectC57BL/6en_US
dc.subjectEAEen_US
dc.subjectmultiple sclerosisen_US
dc.subjectTNF-alphaen_US
dc.subjectcaspase 3en_US
dc.subjectglycyrrhetinic aciden_US
dc.subjectinterleukin 17en_US
dc.subjectinterleukin 1betaen_US
dc.subjecttumor necrosis factoren_US
dc.subject18alpha-glycyrrhetinic aciden_US
dc.subjectCasp3 protein, mouseen_US
dc.subjectcytokineen_US
dc.subjectanimal experimenten_US
dc.subjectanimal modelen_US
dc.subjectArticleen_US
dc.subjectbiochemical analysisen_US
dc.subjectbrain tissueen_US
dc.subjectclinical featureen_US
dc.subjectcontrolled studyen_US
dc.subjectexperimental autoimmune encephalomyelitisen_US
dc.subjectfemaleen_US
dc.subjecthistologyen_US
dc.subjecthistopathologyen_US
dc.subjectlipid peroxidationen_US
dc.subjectmouseen_US
dc.subjectnonhumanen_US
dc.subjectoxidative stressen_US
dc.subjectpriority journalen_US
dc.subjectanalogs and derivativesen_US
dc.subjectanimalen_US
dc.subjectbrainen_US
dc.subjectchemically induceden_US
dc.subjectdrug effecten_US
dc.subjectmetabolismen_US
dc.subjectpathologyen_US
dc.subjectAnimalsen_US
dc.subjectBrainen_US
dc.subjectCaspase 3en_US
dc.subjectCytokinesen_US
dc.subjectEncephalomyelitis, Autoimmune, Experimentalen_US
dc.subjectFemaleen_US
dc.subjectGlycyrrhetinic Aciden_US
dc.subjectLipid Peroxidationen_US
dc.subjectMiceen_US
dc.subjectOxidative Stressen_US
dc.titleThe beneficial effects of 18ß-glycyrrhetinic acid on the experimental autoimmune encephalomyelitis (EAE) in C57BL/6 mouse modelen_US
dc.typeArticleen_US
dc.identifier.volume40en_US
dc.identifier.issue4en_US
dc.identifier.startpage344
dc.identifier.startpage344en_US
dc.identifier.endpage352en_US
dc.identifier.doi10.1080/08923973.2018.1490318-
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.identifier.pmid30052483en_US
dc.identifier.scopus2-s2.0-85050989401en_US
dc.identifier.wosWOS:000444439100013en_US
dc.identifier.scopusqualityQ2-
dc.ownerPamukkale University-
item.grantfulltextnone-
item.fulltextNo Fulltext-
item.cerifentitytypePublications-
item.openairetypeArticle-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.languageiso639-1en-
crisitem.author.dept14.02. Internal Medicine-
Appears in Collections:PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection
Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
Tıp Fakültesi Koleksiyonu
WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection
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