Please use this identifier to cite or link to this item: https://hdl.handle.net/11499/10952
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dc.contributor.authorÇiftçi, Osman-
dc.contributor.authorDuman, A.S.-
dc.contributor.authorTurkmen, N.B.-
dc.contributor.authorTaslıdere, A.-
dc.date.accessioned2019-08-16T13:34:04Z
dc.date.available2019-08-16T13:34:04Z
dc.date.issued2018-
dc.identifier.issn1984-8250-
dc.identifier.urihttps://hdl.handle.net/11499/10952-
dc.identifier.urihttps://doi.org/10.1590/s2175-97902018000317674-
dc.description.abstract2,3,7,8-Tetrachlorodibenzo-p-dioxin (TCDD) is a widespread environmental contaminant which causes severe toxic effects. Despite there is some suggestion concerning with TCDD induced cardiotoxicity such as formation of free radicals, the main mechanism has not been entirely explained. Beta-glucan is known as strong antioxidant matter and can scavenge free radicals. Therefore this study aimed to investigate the protective effects of beta-glucan against TCDD induced cardiotoxicity in rats. In this study, 2-3 months of age and 190-250 g in weight 32 rats were randomly divided into four equal groups (n=8 for each group). Group 1 was control; Group 2 was TCDD group (2 µg/kg/week); group 3 was the beta-glucan group(50 mg/kg/day), and group 4 was TCDD and beta-glucan treatment group. The heart samples were taken from rats after 21 days treatment. The results were shown that Despite TCDD exposure visibly caused to increase (p ? 0.001) in TBARS levels, It caused a visible decline in the levels of GSH, CAT, GSH-Px, and SOD. However Beta glucan significantly increased GSH, CAT, GSH-Px, SOD levels and decreased generation of TBARS. Additionally, our histopathological observations were in agreement with the biochemical results. In conclusion, Beta-glucan treatment exhibited protective activity on TCDD induced cardiotoxicity. © 2018, Faculdade de Ciencias Farmaceuticas (Biblioteca). All rights reserved.en_US
dc.language.isoenen_US
dc.publisherFaculdade de Ciencias Farmaceuticas (Biblioteca)en_US
dc.relation.ispartofBrazilian Journal of Pharmaceutical Sciencesen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subject2, 3, 7, 8-tetrachlorodibenzo-p-dioxin (TCDD)en_US
dc.subjectBeta-glucan/protective effectsen_US
dc.subjectCardiotoxicityen_US
dc.subjectRatsen_US
dc.subject2,3,7,8 tetrachlorodibenzo para dioxinen_US
dc.subjectbeta glucanen_US
dc.subjectcatalaseen_US
dc.subjectglutathioneen_US
dc.subjectglutathione peroxidaseen_US
dc.subjectsuperoxide dismutaseen_US
dc.subjectthiobarbituric acid reactive substanceen_US
dc.subjectadulten_US
dc.subjectanimal experimenten_US
dc.subjectanimal tissueen_US
dc.subjectArticleen_US
dc.subjectcardiotoxicityen_US
dc.subjectcontrolled studyen_US
dc.subjectfemaleen_US
dc.subjectheart injuryen_US
dc.subjectheart protectionen_US
dc.subjectheart tissueen_US
dc.subjecthistopathologyen_US
dc.subjectnonhumanen_US
dc.subjectoxidative stressen_US
dc.subjectraten_US
dc.titleBeta-glucan prevents toxic effects of 2,3,7,8-TCDD in terms of oxidative and histopathological damage in heart tissue of ratsen_US
dc.typeArticleen_US
dc.identifier.volume54en_US
dc.identifier.issue3en_US
dc.identifier.doi10.1590/s2175-97902018000317674-
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.identifier.scopus2-s2.0-85059273272en_US
dc.identifier.wosWOS:000452199300001en_US
dc.identifier.scopusqualityQ2-
dc.ownerPamukkale University-
item.languageiso639-1en-
item.grantfulltextopen-
item.fulltextWith Fulltext-
item.cerifentitytypePublications-
item.openairetypeArticle-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
crisitem.author.dept14.02. Internal Medicine-
Appears in Collections:Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
Tıp Fakültesi Koleksiyonu
WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection
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