Publication:
Effect of black tea on lipid peroxidation in carbon tetrachloride treated male rats

dc.contributor.authorsSür-Altiner D., Yenice B.
dc.date.accessioned2022-03-15T01:54:00Z
dc.date.accessioned2026-01-10T19:25:57Z
dc.date.available2022-03-15T01:54:00Z
dc.date.issued2000
dc.description.abstractThis study examined the effects of black tea (Camellia sinensis L.) on lipid peroxidation and glutathione levels in carbon tetrachloride (CCl4)- treated male Wistar rats. Three groups of rats formed two control groups and one treatment group. The control groups were fed with a standard diet, while the black tea group were fed the standard diet plus 6% by weight dried black tea leaves. After two months, the rats in the black tea group and in one control group were administered a single dose of CCl4 (1 ml/kg, i.p.) and sacrificed two hours later. Rats in the other control group were administered olive oil in a similar fashion. Lipid peroxide levels in liver and plasma, glutathione (GSH) levels in liver and alanine transaminase (ALT) and aspartate transaminase (AST) activities in plasma were measured. Rats in the black tea group were found to have significantly decreased liver lipid peroxide levels, and ALT and AST activities compared with the rats in the CCl4-treated control group. In addition, liver glutathione levels were decreased in the black tea group. These data suggest that black tea attenuates CCl4-induced hepatic injury.
dc.identifier.doi10.1515/DMDI.2000.16.2.123
dc.identifier.issn7925077
dc.identifier.pubmed10962644
dc.identifier.urihttps://hdl.handle.net/11424/246446
dc.language.isoeng
dc.publisherFreund Publishing House Ltd
dc.relation.ispartofDrug Metabolism and Drug Interactions
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectALT
dc.subjectAST
dc.subjectBlack tea
dc.subjectGlutathione
dc.subjectLipid peroxidation
dc.titleEffect of black tea on lipid peroxidation in carbon tetrachloride treated male rats
dc.typearticle
dspace.entity.typePublication
oaire.citation.endPage128
oaire.citation.issue2
oaire.citation.startPage123
oaire.citation.titleDrug Metabolism and Drug Interactions
oaire.citation.volume16

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