Please use this identifier to cite or link to this item: http://earsiv.odu.edu.tr:8080/xmlui/handle/11489/4588
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dc.contributor.authorCirrik, Selma-
dc.contributor.authorHacioglu, Gulay-
dc.contributor.authorCokeli, Emel Kabartan-
dc.contributor.authorPeker, Emine Gulceri Gulec-
dc.date.accessioned2024-03-15T11:54:45Z-
dc.date.available2024-03-15T11:54:45Z-
dc.date.issued2024-
dc.identifier.citationCirrik, S., Hacioglu, G., Cokeli, EK., Peker, EGG. (2024). Antioxidant efficiency of Prunus laurocerasus L. fruit extract on doxorubicin induced hepatic and renal damage. Indian J. Exp. Biol., 62(2), 103-111. https://doi.org/10.56042/ijeb.v62i02.4286en_US
dc.identifier.issn0019-5189-
dc.identifier.issn0975-1009-
dc.identifier.urihttp://dx.doi.org/10.56042/ijeb.v62i02.4286-
dc.identifier.urihttps://www.webofscience.com/wos/woscc/full-record/WOS:001158401800005-
dc.identifier.urihttp://earsiv.odu.edu.tr:8080/xmlui/handle/11489/4588-
dc.descriptionWoS Categories: Biologyen_US
dc.descriptionWeb of Science Index: Science Citation Index Expanded (SCI-EXPANDED)en_US
dc.descriptionResearch Areas: Life Sciences & Biomedicine - Other Topicsen_US
dc.description.abstractIn Turkish traditional medicine, the leaves, fruit and seeds of Prunus laurocerasus L., commonly called Cherry laurel, are used to treat various diseases such as cancer, diabetes, influenza, tonsillitis and scalp dandruff. The medicinal value of this plant can be attributed to its rich phenolic content and high antioxidant capacity. In this study, we investigated the efficacy of P. laurocerasus (PL) fruit extract in reducing the hepatorenal side effects of doxorubicin (DOX). SpragueDawley rats were divided into 4 groups as Control, DOX, PL500+DOX and PL1000+DOX (n=8). PL -extracts were given perorally for two weeks (500 or 1000 mg.kg(-1).day(-1)). After 48-h of DOX injection (15 mg/kg, i.p.), the animals were sacrificed. Compared to control, in DOX group, we observed lower levels of serum albumin, higher alanine transaminase (ALT), aspartate transaminase (AST) and creatinine levels (P <0.001 for each one); decreased Glomerular filtration rate (GFR) (P <0.01); increased urinary neutrophil gelatinase-associated lipocalin (P <0.01); and kidney injury molecule -1 (P <0.001) levels. DOX-induced hepatorenal oxidative stress was approved by increased malondialdehyde (MDA) and decreased glutathione (GSH) levels and decreased superoxide dismutase (SOD) and catalase (CAT) (P <0.001 for each one) activities. Although PL -treatment did not change serum and urinary parameters, it significantly returned hepatic MDA and GSH levels, SOD and CAT activities (P <0.001 for each one) as well as renal MDA (P <0.001) and GSH (P <0.05) levels and CAT activity (P <0.001) to control levels. While high dose PL provided a more significant (P <0.05) reduction in renal lipid peroxidation, it did not significantly affect other parameters. With these observations, it can be suggested that rather than increasing the dose, a longer duration of PL treatment after DOX induction may be more effective in preventing tissue damage and oxidative stress.en_US
dc.description.sponsorshipOrdu University [A-2101]en_US
dc.language.isoengen_US
dc.publisherNATL INST SCIENCE COMMUNICATION-NISCAIR-NEW DELHIen_US
dc.relation.isversionof10.56042/ijeb.v62i02.4286en_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectAlbumin, Cherry laurel, Creatinine, Glomerular filtration rate (GFR), Kidney injury molecule-1 (Kim-1), Liver, Neutrophil gelatinase-associated lipocalin (NGAL), Oxidative stress, Reactive oxygen species (ROS), Tissue damageen_US
dc.subjectOXIDATIVE STRESS, INDUCED NEPHROTOXICITY, LEAF EXTRACT, HYPERGLYCEMIA, APOPTOSIS, PROPOLISen_US
dc.titleAntioxidant efficiency of Prunus laurocerasus L. fruit extract on doxorubicin induced hepatic and renal damageen_US
dc.typearticleen_US
dc.relation.journalINDIAN JOURNAL OF EXPERIMENTAL BIOLOGYen_US
dc.contributor.departmentOrdu Üniversitesien_US
dc.contributor.authorID0000-0002-6289-2310en_US
dc.identifier.volume62en_US
dc.identifier.issue2en_US
dc.identifier.startpage103en_US
dc.identifier.endpage111en_US
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