Caffeic acid phenethyl ester protects rabbit brains against permanent focal ischemia by antioxidant action: A biochemical and planimetric study

dc.contributor.authorAltug, Muhammed Enes
dc.contributor.authorSerarslan, Yurdal
dc.contributor.authorBal, Ramazan
dc.contributor.authorKontas, Tuenay
dc.contributor.authorEkici, Fatih
dc.contributor.authorMelek, Ismet M.
dc.contributor.authorDuman, Taskin
dc.date.accessioned2026-08-12T17:13:49Z
dc.date.issued2008
dc.departmentFırat Üniversitesi
dc.description.abstractThe present study was conducted to investigate whether caffeic acid phenethyl ester (CAPE), an active component of propolis extract, has a protective effect on brain injury after focal permanent cerebral ischemia, and to determine the possible antioxidant mechanisms. Cerebral infarction in adult male New Zealand rabbits was induced by microsurgical procedures producing right focal permanent middle cerebral artery occlusion (pMCAO). CAPE was administered to the treatment group after pMCAO at a dose of 10 mu mol kg(-1) once a day intraperitoneally for 7 days. Neurological deficits were evaluated, using a modified six-point scale. Spectrophotometric assay was used to determine the contents of malondialdehyde (MDA), glutathione (GSH), catalase (CAT), nitric oxide (NO) and xanthine oxidase (XO). In the ipsilateral hemisphere, the infarct volume of the brain was assessed in brain slices stained with heamatoxylen and eosin. The results showed that treatment with CAPE significantly reduced the percentage of infarction in the ipsilateral hemisphere compared with the ischemia group. CAPE treatment significantly attenuated the elevation of plasma MDA, CAT and XO content (p < 0.05), whereas it significantly increased the levels of plasma GSH and NO (p < 0.05). Therefore, subacute CAPE administration plays a protective role in focal pMCAO due to attenuation of lipid peroxidation and its antioxidant activity. All of these findings suggest that CAPE provides neuroprotection against cerebral ischemia injury through its antioxidant action. (C) 2008 Elsevier B.V. All rights reserved.
dc.identifier.doi10.1016/j.brainres.2008.01.053
dc.identifier.endpage142
dc.identifier.issn0006-8993
dc.identifier.issn1872-6240
dc.identifier.orcid0000-0003-3829-8669
dc.identifier.orcid0000-0002-6552-4193
dc.identifier.pmid18308295
dc.identifier.scopus2-s2.0-40849101557
dc.identifier.scopusqualityQ2
dc.identifier.startpage135
dc.identifier.urihttps://doi.org/10.1016/j.brainres.2008.01.053
dc.identifier.urihttps://hdl.handle.net/11508/51559
dc.identifier.volume1201
dc.identifier.wosWOS:000255065600017
dc.identifier.wosqualityQ3
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.indekslendigikaynakPubMed
dc.language.isoen
dc.publisherElsevier
dc.relation.ispartofBrain Research
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.snmzKA_WoS_20260511
dc.subjectcaffeic acid phenethyl ester
dc.subjectantioxidant activity
dc.subjectfocal permanent cerebral ischemia
dc.subjectneuroprotection
dc.subjectrabbit
dc.titleCaffeic acid phenethyl ester protects rabbit brains against permanent focal ischemia by antioxidant action: A biochemical and planimetric study
dc.typeArticle

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