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

dc.authorscopusid 57196052987
dc.authorscopusid 57564895300
dc.authorscopusid 6504603410
dc.authorscopusid 6701546641
dc.authorscopusid 8368813400
dc.authorscopusid 55662834600
dc.contributor.author Şener, Göksel
dc.contributor.author Turan, F.B.
dc.contributor.author Ozbeyli, D.
dc.contributor.author Yanardag, R.
dc.contributor.author Sacan, O.
dc.contributor.author Sener, G.
dc.contributor.other Eczacılık Meslek Bilimleri Bölümü
dc.date.accessioned 2025-01-11T13:04:50Z
dc.date.available 2025-01-11T13:04:50Z
dc.date.issued 2021
dc.department Fenerbahçe University en_US
dc.department-temp Ertas 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, Turkey en_US
dc.description.abstract Objective: 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.citation 7
dc.identifier.doi 10.26650/EurJBiol.2021.1023136
dc.identifier.endpage 178 en_US
dc.identifier.issn 2602-2575
dc.identifier.issue 2 en_US
dc.identifier.scopus 2-s2.0-85127692356
dc.identifier.scopusquality Q4
dc.identifier.startpage 173 en_US
dc.identifier.uri https://doi.org/10.26650/EurJBiol.2021.1023136
dc.identifier.uri https://hdl.handle.net/20.500.14627/403
dc.identifier.volume 80 en_US
dc.identifier.wosquality N/A
dc.language.iso en en_US
dc.publisher Istanbul University Press en_US
dc.relation.ispartof European Journal of Biology en_US
dc.relation.publicationcategory Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı en_US
dc.rights info:eu-repo/semantics/openAccess en_US
dc.scopus.citedbyCount 9
dc.subject Anti-Inflammatory en_US
dc.subject Hepatotoxicity en_US
dc.subject Methotrexate en_US
dc.subject Oxidative Injury en_US
dc.subject Petroselinum Crispum en_US
dc.title Protective Effects of Petroselinum Crispum (parsley) Extract Against Methotrexate-Induced Hepatotoxicity en_US
dc.type Article en_US
dspace.entity.type Publication
relation.isAuthorOfPublication 68ac39be-51c5-4820-a6c9-0bef06348d93
relation.isAuthorOfPublication.latestForDiscovery 68ac39be-51c5-4820-a6c9-0bef06348d93
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relation.isOrgUnitOfPublication.latestForDiscovery 5052e089-e75d-4aec-a280-6353973e4819

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