Protective Effects of Petroselinum Crispum (parsley) Extract Against Methotrexate-Induced Hepatotoxicity

dc.authorscopusid57196052987
dc.authorscopusid57564895300
dc.authorscopusid6504603410
dc.authorscopusid6701546641
dc.authorscopusid8368813400
dc.authorscopusid55662834600
dc.contributor.authorŞener, Göksel
dc.contributor.authorTuran, F.B.
dc.contributor.authorOzbeyli, D.
dc.contributor.authorYanardag, R.
dc.contributor.authorSacan, O.
dc.contributor.authorSener, G.
dc.contributor.otherEczacılık Meslek Bilimleri Bölümü
dc.date.accessioned2025-01-11T13:04:50Z
dc.date.available2025-01-11T13:04:50Z
dc.date.issued2021
dc.departmentFenerbahçe Universityen_US
dc.department-tempErtas B., Marmara University, School of Pharmacy, Department of Pharmacology, Istanbul, Turkey; Turan F.B., Marmara University, School of Pharmacy, Department of Pharmacology, Istanbul, Turkey; Ozbeyli D., Marmara University, Vocational School of Health Services, Medical Pathology Techniques, Istanbul, Turkey; Yanardag R., Istanbul University, Faculty of Engineering, Department of Biochemistry, Istanbul, Turkey; Sacan O., Istanbul University, Faculty of Engineering, Department of Biochemistry, Istanbul, Turkey; Sener G., Fenerbahce University, Vocational School of Health Services, Istanbul, Turkeyen_US
dc.description.abstractObjective: By inhibiting the synthesis of thymidine and purine, and thereby DNA synthesis, Methotrexate (MTX), suppresses the proliferation of cancer cells. It is thought that the side-effect mechanism is related to oxidant molecules derived from MTX metabolism. In this study, we examined whether the Petroselinum crispum extracts (PCr; parsley) of which the antioxidant properties have been previously shown, was protective against MTX induced liver damage. Materials and Methods: Sprague Dawley rats (female/male; 200-250 g) were used. MTX was injected intraperitoneally and PCr extract was given orally. A single dose of 20mg/kg MTX was administered to the groups that were to experience hepatotoxicity. Then, a physiological saline (MTX group) or PCr (2 g/kg, MTX + PCr group) treatment was applied for 5 days. The same treatments were applied to the other groups (control group, PCr group) for 5 days after a single dose saline injection. At the end of the study, the biochemical parameters were examined in the blood and liver tissues taken from animals sacrificed by decapitation. Results: MTX caused a significant increase in malondialdehyde and collagen levels and myeloperoxidase and caspase-3 activities, while glutathione levels were found to have decreased. PCr treatment showed protective efficacy by preventing these increases. Conclusion: It appears that the administration of PCr to MTX treated rats prevented the accumulation of lipid peroxides, inflamatory reactions and depletion of antioxidant glutathione, and thus protected liver tissues against oxidative stress. © 2021 European Journal of Biology. All rights reserved.en_US
dc.identifier.citation7
dc.identifier.doi10.26650/EurJBiol.2021.1023136
dc.identifier.endpage178en_US
dc.identifier.issn2602-2575
dc.identifier.issue2en_US
dc.identifier.scopus2-s2.0-85127692356
dc.identifier.scopusqualityQ4
dc.identifier.startpage173en_US
dc.identifier.urihttps://doi.org/10.26650/EurJBiol.2021.1023136
dc.identifier.urihttps://hdl.handle.net/20.500.14627/403
dc.identifier.volume80en_US
dc.identifier.wosqualityN/A
dc.language.isoenen_US
dc.publisherIstanbul University Pressen_US
dc.relation.ispartofEuropean Journal of Biologyen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectAnti-Inflammatoryen_US
dc.subjectHepatotoxicityen_US
dc.subjectMethotrexateen_US
dc.subjectOxidative Injuryen_US
dc.subjectPetroselinum Crispumen_US
dc.titleProtective Effects of Petroselinum Crispum (parsley) Extract Against Methotrexate-Induced Hepatotoxicityen_US
dc.typeArticleen_US
dspace.entity.typePublication
relation.isAuthorOfPublication68ac39be-51c5-4820-a6c9-0bef06348d93
relation.isAuthorOfPublication.latestForDiscovery68ac39be-51c5-4820-a6c9-0bef06348d93
relation.isOrgUnitOfPublication5052e089-e75d-4aec-a280-6353973e4819
relation.isOrgUnitOfPublication.latestForDiscovery5052e089-e75d-4aec-a280-6353973e4819

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