The effect of Hippophae rhamnoides extract on ischemia reperfusion-induced brain injury in rats

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The aim of this study was to examine the effects of Hippophae rhamnoides extract (HRE), known to have antioxidant properties, on ischemia reperfusion-induced brain injury in rats. Eighteen albino Wistar male rats were divided into three equal groups: 15 min of brain ischemia-3 h of reperfusion (BIR) group, 50 mg/kg HRE + brain ischemia-reperfusion (HRE + BIR) group, and control group for sham operation (SHAM). Malondialdehyde (MDA) level, myeloperoxidase (MPO) activity and 8-OHdG levels significantly increased, whereas total glutathione (tGSH) level, glutathione reductase (GSHRd), glutathione s-transferase (GST) activities decreased in the brain tissues of BIR group compared to SHAM group. HR application reversed these changes and brought the levels closer to the level of SHAM group. This study has revealed that HR inhibits IR-induced oxidative damage and inflammation in rat’s brain biochemically and it is effective in maintaining antioxidant activity and protecting against DNA damage in the tissue. © 2019, Colegio de Farmaceuticos de la Provincia de Buenos Aires. All rights reserved.

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AlanDeğerDil
dc.contributor.authorOzbek Bilgin, Asli
dc.contributor.authorAltuner, Durdu
dc.contributor.authorCankaya, Murat
dc.contributor.authorCakir, Tayfun
dc.contributor.authorMammadov, Renad
dc.contributor.authorBilgin, Yasin
dc.contributor.authorSüleyman, Halis
dc.date.accessioned2026-10-18T20:28:55.759345310Z
dc.date.available2026-10-18T20:28:55.759345310Z
dc.date.issued2019
dc.description.abstractThe aim of this study was to examine the effects of Hippophae rhamnoides extract (HRE), known to have antioxidant properties, on ischemia reperfusion-induced brain injury in rats. Eighteen albino Wistar male rats were divided into three equal groups: 15 min of brain ischemia-3 h of reperfusion (BIR) group, 50 mg/kg HRE + brain ischemia-reperfusion (HRE + BIR) group, and control group for sham operation (SHAM). Malondialdehyde (MDA) level, myeloperoxidase (MPO) activity and 8-OHdG levels significantly increased, whereas total glutathione (tGSH) level, glutathione reductase (GSHRd), glutathione s-transferase (GST) activities decreased in the brain tissues of BIR group compared to SHAM group. HR application reversed these changes and brought the levels closer to the level of SHAM group. This study has revealed that HR inhibits IR-induced oxidative damage and inflammation in rat’s brain biochemically and it is effective in maintaining antioxidant activity and protecting against DNA damage in the tissue. © 2019, Colegio de Farmaceuticos de la Provincia de Buenos Aires. All rights reserved.
dc.identifier.endpage2462
dc.identifier.issn0326-2383
dc.identifier.issue12
dc.identifier.scopus2-s2.0-85077842590
dc.identifier.startpage2455
dc.identifier.urihttps://rdlopen.rawdatalibrary.net/r/ebyu/14142
dc.identifier.volume38
dc.language.isoen
dc.publisherColegio de Farmaceuticos de la Provincia de Buenos Aires
dc.relation.ispartofLatin American Journal of Pharmacy
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectBrain
dc.subjectHippophae rhamnoides
dc.subjectIschemia reperfusion injury
dc.subjectRat
dc.subjectglutathione
dc.subjectglutathione reductase
dc.subjectglutathione transferase
dc.subjectHippophae rhamnoides extract
dc.subjectmalonaldehyde
dc.subjectmyeloperoxidase
dc.subjectreactive oxygen metabolite
dc.subjectthiobarbituric acid reactive substance
dc.subjectanimal experiment
dc.subjectanimal model
dc.subjectanimal tissue
dc.subjectantiinflammatory activity
dc.subjectantioxidant activity
dc.subjectArticle
dc.subjectbiochemical analysis
dc.subjectbiochemistry
dc.subjectcerebral ischemia reperfusion injury
dc.subjectcontrolled study
dc.subjectDNA damage
dc.subjectDNA determination
dc.subjectelectrochemical detection
dc.subjectenzyme activity
dc.subjecthigh performance liquid chromatography
dc.subjectmale
dc.subjectnonhuman
dc.subjectoxidative stress
dc.titleThe effect of Hippophae rhamnoides extract on ischemia reperfusion-induced brain injury in rats
dc.typeArticle
dspace.entity.typePublication
rdl.citation.scopus0
rdl.source.indexSCOPUS