Please use this identifier to cite or link to this item: https://hdl.handle.net/11499/50451
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dc.contributor.authorTürkmen, Neşe Başak-
dc.contributor.authorYüce, Hande-
dc.contributor.authorTaşlıdere, Aslı-
dc.contributor.authorŞahin, Yasemin-
dc.contributor.authorAyhan, İdris-
dc.contributor.authorÜnüvar, Songül-
dc.contributor.authorÇiftci, Osman-
dc.date.accessioned2023-04-08T10:00:03Z-
dc.date.available2023-04-08T10:00:03Z-
dc.date.issued2022-
dc.identifier.issn1984-8250-
dc.identifier.issn2175-9790-
dc.identifier.urihttps://doi.org/10.1590/s2175-97902022e21219-
dc.identifier.urihttps://hdl.handle.net/11499/50451-
dc.description.abstractThe aim of the preŞent study is to investigate the cardioprotective effects of 1813-glycyrrhetinic acid (1813-GA) against oxidative and histological damage caused by global cerebral ischemia/ reperfusion (I/R) in C57BL/J6 mice. All male mice (n:40) were randomly divided into four groups: (1) sham-operated (Sham), (2) I/R, (3) 1813-GA, and (4) 1813-GA+I/R. Ischemia was not applied to the sham and 1813-GA groups. In the I/R group, the bilateral carotid arteries were clipped for 15 min to induce ischemia, and the mice were treated with the vehicle for 10 days. In the 1813-GA group, the mice were given 1813-GA (100 mg/kg) for 10 days following a median İncision without carotid occlusion. In the 1813-GA+I/R group, the ischemic procedure performed to the I/R model was applied to the animals and afterwards they were intraperitoneally (i.p.) treated with 1813-GA (100 mg/kg) for 10 days. It was found that global cerebral I/R increased TBARS levels and decreased antioxidant parameters. The 1813-GA treatment decreased the level of TBARS and increased GSH, GPx, CAT, SOD activities. Also, the control group cardiac tissue samples were observed to have a normal histological appearance with the Hematoxylin-Eosin staining method. Histopathological damage was observed in the heart tissue samples belonging to the I/R group. The 1813-GA treatment ameliorates oxidative and histological injury in the heart tissue after global ischemia reperfusion, and may be a beneficial alternative treatment.en_US
dc.language.isoenen_US
dc.publisherUniv Sao Paulo, Conjunto Quimicasen_US
dc.relation.ispartofBrazilian Journal of Pharmaceutical Sciencesen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectGlobal cerebral Ien_US
dc.subjectRen_US
dc.subject1813-glycyrrhetinic aciden_US
dc.subjectOxidative stressen_US
dc.subjectHeart injuryen_US
dc.subjectIschemia-Reperfusion Injuryen_US
dc.subjectMechanismsen_US
dc.subjectProtectsen_US
dc.subjectMyrceneen_US
dc.subjectModelen_US
dc.subjectAssayen_US
dc.title18 beta-glycyrrhetinic acid attenuates global cerebral ischemia/reperfusion-induced cardiac damage in C57BL/J6 miceen_US
dc.typeArticleen_US
dc.identifier.volume58en_US
dc.departmentPamukkale Universityen_US
dc.identifier.doi10.1590/s2175-97902022e21219-
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.authorscopusid57211524435-
dc.authorscopusid57222505412-
dc.authorscopusid57192546285-
dc.authorscopusid57209747802-
dc.authorscopusid57201614442-
dc.authorscopusid26024440900-
dc.authorscopusid27867577100-
dc.identifier.scopus2-s2.0-85146521928en_US
dc.identifier.wosWOS:000924004500001en_US
dc.institutionauthor-
dc.identifier.scopusqualityQ2-
item.languageiso639-1en-
item.openairetypeArticle-
item.grantfulltextnone-
item.cerifentitytypePublications-
item.fulltextNo Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
crisitem.author.dept14.02. Internal Medicine-
crisitem.author.dept14.02. Internal Medicine-
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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