Protective effects of vitamin E on carbon tetrachloride-induced liver damage in rats

dc.contributor.authorNaziroglu, M
dc.contributor.authorÇay, M
dc.contributor.authorÜstündag, B
dc.contributor.authorAksakal, M
dc.contributor.authorYekeler, H
dc.date.accessioned2026-08-12T17:10:49Z
dc.date.issued1999
dc.departmentFırat Üniversitesi
dc.description.abstractIn this study we investigated whether the increase of hepatic vitamin E content by intraperitoneal administration, influences chronic liver damage induced by carbon tetrachloride (CCl4) in rats. Thirty adult male Wistar rats were divided into three groups. The first group was used as a control and the rats in the second group were administered CCl4 in olive oil subcutaneously. Rats in the third group were administered intraperitoneally vitamin E (dl-alpha-tocopherol acetate, 100 mg kg(-1)). This administration was performed three times per week for five weeks. Liver samples were used for the determination of vitamin E levels, glutathione peroxidase (GSHPx) activities and histological examination. Serum levels of alanine aminotransferase, lactate dehydrogenase, alkaline phosphatase, aspartate amino transferase, gamma-glutamyltranspeptidase, total and conjugated bilirubin were significantly (p < 005, p < 0.01, p < 0.001) higher in animals treated with CCl4 than in the controls and had returned to normal values by the administration of vitamin E + CCl4. Liver vitamin E levels were significantly (p < 0.05) lower in the CCl4 group than in he control group. However, the liver vitamin E content was significantly (p < 0.01, p < 0.001) increased in the vitamin E + CCl4 injected group. On the other hand, liver GSHPx activity was not statistically different among the groups. On histological examination, vitamin E administered animals showed incomplete, but significant, prevention of liver necrosis and cirrhosis induced by CCl4. these data indicate that intraperitoneally administered vitamin E has protective effects against CCl4-induced chronic liver damage and cirrhosis as evidenced by biochemical data and conventional histological examination. Copyright (C) 1999 John Wiley & Sons, Ltd.
dc.identifier.doi10.1002/(SICI)1099-0844(199912)17:4<253
dc.identifier.endpage259
dc.identifier.issn0263-6484
dc.identifier.issn1099-0844
dc.identifier.issue4
dc.identifier.orcid0000-0003-0887-6974
dc.identifier.orcid0000-0001-6621-2450
dc.identifier.pmid10587612
dc.identifier.scopus2-s2.0-0344577858
dc.identifier.scopusqualityQ3
dc.identifier.startpage253
dc.identifier.urihttps://doi.org/10.1002/(SICI)1099-0844(199912)17:4<253
dc.identifier.urihttps://hdl.handle.net/11508/50898
dc.identifier.volume17
dc.identifier.wosWOS:000084033100004
dc.identifier.wosqualityQ3
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.indekslendigikaynakPubMed
dc.language.isoen
dc.publisherWiley
dc.relation.ispartofCell Biochemistry and Function
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.snmzKA_WoS_20260511
dc.subjectvitamin E
dc.subjectglutathione peroxidase
dc.subjectcirrhosis
dc.subjectliver damage
dc.subjectCCl4
dc.subjectfree radicals
dc.subjectbiochemical and haematological parameters
dc.subjectrat
dc.titleProtective effects of vitamin E on carbon tetrachloride-induced liver damage in rats
dc.typeArticle

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