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Antioxidant efficiency of Prunus laurocerasus L. fruit extract on doxorubicin induced hepatic and renal damage

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dc.contributor.author Cirrik, Selma
dc.contributor.author Hacioglu, Gulay
dc.contributor.author Cokeli, Emel Kabartan
dc.contributor.author Peker, Emine Gulceri Gulec
dc.date.accessioned 2024-03-15T11:54:45Z
dc.date.available 2024-03-15T11:54:45Z
dc.date.issued 2024
dc.identifier.citation Cirrik, 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.v62i02.4286 en_US
dc.identifier.issn 0019-5189
dc.identifier.issn 0975-1009
dc.identifier.uri http://dx.doi.org/10.56042/ijeb.v62i02.4286
dc.identifier.uri https://www.webofscience.com/wos/woscc/full-record/WOS:001158401800005
dc.identifier.uri http://earsiv.odu.edu.tr:8080/xmlui/handle/11489/4588
dc.description WoS Categories: Biology en_US
dc.description Web of Science Index: Science Citation Index Expanded (SCI-EXPANDED) en_US
dc.description Research Areas: Life Sciences & Biomedicine - Other Topics en_US
dc.description.abstract In 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.sponsorship Ordu University [A-2101] en_US
dc.language.iso eng en_US
dc.publisher NATL INST SCIENCE COMMUNICATION-NISCAIR-NEW DELHI en_US
dc.relation.isversionof 10.56042/ijeb.v62i02.4286 en_US
dc.rights info:eu-repo/semantics/openAccess en_US
dc.subject Albumin, 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 damage en_US
dc.subject OXIDATIVE STRESS, INDUCED NEPHROTOXICITY, LEAF EXTRACT, HYPERGLYCEMIA, APOPTOSIS, PROPOLIS en_US
dc.title Antioxidant efficiency of Prunus laurocerasus L. fruit extract on doxorubicin induced hepatic and renal damage en_US
dc.type article en_US
dc.relation.journal INDIAN JOURNAL OF EXPERIMENTAL BIOLOGY en_US
dc.contributor.department Ordu Üniversitesi en_US
dc.contributor.authorID 0000-0002-6289-2310 en_US
dc.identifier.volume 62 en_US
dc.identifier.issue 2 en_US
dc.identifier.startpage 103 en_US
dc.identifier.endpage 111 en_US


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