Ellagic acid impedes carbontetrachloride-induced liver damage in rats through suppression of NF-kB, Bcl-2 and regulating Nrf-2 and caspase pathway

dc.contributor.authorAslan, Abdullah
dc.contributor.authorGok, Ozlem
dc.contributor.authorErman, Orhan
dc.contributor.authorKuloglu, Tuncay
dc.date.accessioned2026-08-12T16:41:25Z
dc.date.issued2018
dc.departmentFırat Üniversitesi
dc.description.abstractThe use of natural antioxidants instead of conventional treatments is considered effective and safe alternative therapy for hepatotoxicity. Ellagic acid (EA) is a strong antioxidant matter having protecting effect particularly on the liver. Hepatotoxic compounds can cause very heavy damage. Among these chemical hepatotoxins, CCl4 are responsible for the trichloromethyl radical resulting from biotransformation of the liver. The aim of this study was to examine whether EA plays a protective role against to liver damage induced with carbon tetrachloride (CCl4) in rats. In this study, 36 male wistar albino (n = 36, 8 weeks old) rats were used. The rats were distributed into 4 groups, and 9 rats involved in each group. The groups were: (i) Control Group: Fed with standard diet; (ii) EA Group: Fed with standard diet + EA; (iii) CCl4 Group: Fed with standard diet + CCl4; (iv) CCl4 + EA Group: Fed with standard diet + CCl4 + EA. After 8 weeks, the rats were decapitated and the liver tissue were examined. As a result; EA application created a significant difference (p < 0.05) on caspase-3, bcl-2, NF-kB and Nrf-2 expression in the CCl4 + EA group in comparison to CCl4 group. Caspase-3 and Nrf-2 expression levels were increased in the CCl4 + EA group in comparison to CCl4 group, but bcl-2 and NF-kB expression levels were decreased. In TUNEL assay examinations, apoptotic index ratio was decreased in the CCl4 + EA group in comparison to CCl4 group. These results show that EA reduce liver damage ratio M wistar albino rats and also these results suggest that ellagic acid may be a potentially protective drug against to liver damage in future.
dc.description.sponsorshipFirat University Scientific Research Projects Unit (FUBAP) [FF.16.42]
dc.description.sponsorshipThe article supported by Firat University Scientific Research Projects Unit (FUBAP) with FF.16.42 project number.
dc.identifier.doi10.1016/j.biopha.2018.06.020
dc.identifier.endpage669
dc.identifier.issn0753-3322
dc.identifier.issn1950-6007
dc.identifier.orcid0000-0001-9874-3838
dc.identifier.orcid0000-0001-8521-6369
dc.identifier.orcid0000-0002-6243-4221
dc.identifier.pmid29902765
dc.identifier.scopus2-s2.0-85048260478
dc.identifier.scopusqualityQ1
dc.identifier.startpage662
dc.identifier.urihttps://doi.org/10.1016/j.biopha.2018.06.020
dc.identifier.urihttps://hdl.handle.net/11508/45825
dc.identifier.volume105
dc.identifier.wosWOS:000438312600075
dc.identifier.wosqualityN/A
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.indekslendigikaynakPubMed
dc.language.isoen
dc.publisherElsevier France-Editions Scientifiques Medicales Elsevier
dc.relation.ispartofBiomedicine & Pharmacotherapy
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.snmzKA_WoS_20260511
dc.subjectEllagic acid
dc.subjectLiver
dc.subjectApoptosis
dc.subjectCaspase-3
dc.subjectBcl-2
dc.subjectNrf-2
dc.subjectNF-kB
dc.titleEllagic acid impedes carbontetrachloride-induced liver damage in rats through suppression of NF-kB, Bcl-2 and regulating Nrf-2 and caspase pathway
dc.typeArticle

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