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https://hdl.handle.net/11499/10711
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DC Field | Value | Language |
---|---|---|
dc.contributor.author | Kamışlı, S. | - |
dc.contributor.author | Çiftçi, Osman | - |
dc.contributor.author | Taşlıdere, A. | - |
dc.contributor.author | Başak Türkmen, N. | - |
dc.contributor.author | Özcan, C. | - |
dc.date.accessioned | 2019-08-16T13:32:33Z | |
dc.date.available | 2019-08-16T13:32:33Z | |
dc.date.issued | 2018 | - |
dc.identifier.issn | 0892-3973 | - |
dc.identifier.uri | https://hdl.handle.net/11499/10711 | - |
dc.identifier.uri | https://doi.org/10.1080/08923973.2018.1490318 | - |
dc.description.abstract | Aim: 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.iso | en | en_US |
dc.publisher | Taylor and Francis Ltd | en_US |
dc.relation.ispartof | Immunopharmacology and Immunotoxicology | en_US |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.subject | 18ß-glycyrrhetinic acid | en_US |
dc.subject | C57BL/6 | en_US |
dc.subject | EAE | en_US |
dc.subject | multiple sclerosis | en_US |
dc.subject | TNF-alpha | en_US |
dc.subject | caspase 3 | en_US |
dc.subject | glycyrrhetinic acid | en_US |
dc.subject | interleukin 17 | en_US |
dc.subject | interleukin 1beta | en_US |
dc.subject | tumor necrosis factor | en_US |
dc.subject | 18alpha-glycyrrhetinic acid | en_US |
dc.subject | Casp3 protein, mouse | en_US |
dc.subject | cytokine | en_US |
dc.subject | animal experiment | en_US |
dc.subject | animal model | en_US |
dc.subject | Article | en_US |
dc.subject | biochemical analysis | en_US |
dc.subject | brain tissue | en_US |
dc.subject | clinical feature | en_US |
dc.subject | controlled study | en_US |
dc.subject | experimental autoimmune encephalomyelitis | en_US |
dc.subject | female | en_US |
dc.subject | histology | en_US |
dc.subject | histopathology | en_US |
dc.subject | lipid peroxidation | en_US |
dc.subject | mouse | en_US |
dc.subject | nonhuman | en_US |
dc.subject | oxidative stress | en_US |
dc.subject | priority journal | en_US |
dc.subject | analogs and derivatives | en_US |
dc.subject | animal | en_US |
dc.subject | brain | en_US |
dc.subject | chemically induced | en_US |
dc.subject | drug effect | en_US |
dc.subject | metabolism | en_US |
dc.subject | pathology | en_US |
dc.subject | Animals | en_US |
dc.subject | Brain | en_US |
dc.subject | Caspase 3 | en_US |
dc.subject | Cytokines | en_US |
dc.subject | Encephalomyelitis, Autoimmune, Experimental | en_US |
dc.subject | Female | en_US |
dc.subject | Glycyrrhetinic Acid | en_US |
dc.subject | Lipid Peroxidation | en_US |
dc.subject | Mice | en_US |
dc.subject | Oxidative Stress | en_US |
dc.title | The beneficial effects of 18ß-glycyrrhetinic acid on the experimental autoimmune encephalomyelitis (EAE) in C57BL/6 mouse model | en_US |
dc.type | Article | en_US |
dc.identifier.volume | 40 | en_US |
dc.identifier.issue | 4 | en_US |
dc.identifier.startpage | 344 | |
dc.identifier.startpage | 344 | en_US |
dc.identifier.endpage | 352 | en_US |
dc.identifier.doi | 10.1080/08923973.2018.1490318 | - |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.identifier.pmid | 30052483 | en_US |
dc.identifier.scopus | 2-s2.0-85050989401 | en_US |
dc.identifier.wos | WOS:000444439100013 | en_US |
dc.identifier.scopusquality | Q2 | - |
dc.owner | Pamukkale University | - |
item.grantfulltext | none | - |
item.fulltext | No Fulltext | - |
item.cerifentitytype | Publications | - |
item.openairetype | Article | - |
item.openairecristype | http://purl.org/coar/resource_type/c_18cf | - |
item.languageiso639-1 | en | - |
crisitem.author.dept | 14.02. 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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