Effect of oleuropein against chemotherapy drug-induced histological changes, oxidative stress, and DNA damages in rat kidney injury

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Özet

Cisplatin-based chemotherapy is responsible for a large number of renal failures, and it is still associated with high rates of mortality today. Oleuropein (OLE) presents a plethora of pharmacological beneficial properties. In this study we investigated whether OLE could provide sufficient protection against cisplatin-induced nephrotoxicity. With this aim, Sprague-Dawley rats were divided into eight groups: control; 7 mg/kg/d cisplatin, 50 mg/kg, 100 mg/kg, and 200 mg/kg OLE; and treatment with OLE for 3 days starting at 24 hours following cisplatin injection. After exposure to the chemotherapy agent and OLE, oxidative DNA damage was quantitated in the renal tissue of experimental animals by measuring the amount of 8-hydroxy-2′-deoxyguanosine (8-OHdG) adducts. Malondialdehyde (MDA) level, total oxidative stress (TOS), and total antioxidant status (TAS) were assessed to determine the oxidative injury in kidney cells. The histology of the kidney was examined using four different staining methods: hematoxylin-eosin (H&E), periodic acid Schiff (PAS), Masson trichrome, and amyloid. In addition, the blood urea nitrogen (BUN), uric acid (UA), and creatinine (CRE) levels were established. Our experimental data showed that tissue 8-OHdG levels were significantly higher in the cisplatin group when compared to the control group. The glomerular cells were sensitive to cisplatin as tubular cells. In addition, treatment with cisplatin elevated the levels of BUN, UA, CRE, and TOS, but lowered the level of TAS compared to the control group. The OLE therapy modulated oxidative stress in order to restore normal kidney function and reduced the formation of 8-OHdG induced by cisplatin. Furthermore, the OLE treatment significantly reduced pathological findings in renal tissue. We demonstrate for the first time that OLE presents significant cytoprotective properties against cisplatin-induced genotoxicity by restoring the antioxidant system of the renal tissue. According to our findings, OLE is a promising novel natural source for the prevention of serious kidney damage in current chemotherapies. © 2016

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RDL Kalıcı Bağlantı (PID)
https://rdlopen.rawdatalibrary.net/r/ebyu/14896Resmi atıflarda kullanılan kalıcı adres
DOI
https://doi.org/10.1016/j.jfda.2016.07.002Yayıncı resmi DOI adresi
Tam Kayıt
AlanDeğerDil
dc.contributor.authorGeyikoglu, Fatime
dc.contributor.authorEmir, Murat
dc.contributor.authorColak, Suat
dc.contributor.authorKoc, Kubra
dc.contributor.authorTurkez, Hasan
dc.contributor.authorBakir, Murat
dc.contributor.authorHosseinigouzdagani, Mirkhalil
dc.contributor.authorCerig, Salim
dc.contributor.authorKeles, Osman Nuri
dc.contributor.authorOzek, Nihal Simsek
dc.date.accessioned2026-10-18T20:29:41.660560609Z
dc.date.available2026-10-18T20:29:41.660560609Z
dc.date.issued2017
dc.description.abstractCisplatin-based chemotherapy is responsible for a large number of renal failures, and it is still associated with high rates of mortality today. Oleuropein (OLE) presents a plethora of pharmacological beneficial properties. In this study we investigated whether OLE could provide sufficient protection against cisplatin-induced nephrotoxicity. With this aim, Sprague-Dawley rats were divided into eight groups: control; 7 mg/kg/d cisplatin, 50 mg/kg, 100 mg/kg, and 200 mg/kg OLE; and treatment with OLE for 3 days starting at 24 hours following cisplatin injection. After exposure to the chemotherapy agent and OLE, oxidative DNA damage was quantitated in the renal tissue of experimental animals by measuring the amount of 8-hydroxy-2′-deoxyguanosine (8-OHdG) adducts. Malondialdehyde (MDA) level, total oxidative stress (TOS), and total antioxidant status (TAS) were assessed to determine the oxidative injury in kidney cells. The histology of the kidney was examined using four different staining methods: hematoxylin-eosin (H&E), periodic acid Schiff (PAS), Masson trichrome, and amyloid. In addition, the blood urea nitrogen (BUN), uric acid (UA), and creatinine (CRE) levels were established. Our experimental data showed that tissue 8-OHdG levels were significantly higher in the cisplatin group when compared to the control group. The glomerular cells were sensitive to cisplatin as tubular cells. In addition, treatment with cisplatin elevated the levels of BUN, UA, CRE, and TOS, but lowered the level of TAS compared to the control group. The OLE therapy modulated oxidative stress in order to restore normal kidney function and reduced the formation of 8-OHdG induced by cisplatin. Furthermore, the OLE treatment significantly reduced pathological findings in renal tissue. We demonstrate for the first time that OLE presents significant cytoprotective properties against cisplatin-induced genotoxicity by restoring the antioxidant system of the renal tissue. According to our findings, OLE is a promising novel natural source for the prevention of serious kidney damage in current chemotherapies. © 2016
dc.description.sponsorshipThis work was financially supported by BAP (accepted in 2015, project no. 2015/94) from Ataturk University.
dc.identifier.doi10.1016/j.jfda.2016.07.002
dc.identifier.endpage459
dc.identifier.issn1021-9498
dc.identifier.issue2
dc.identifier.pmcidPMC9332526
dc.identifier.pmid28911689
dc.identifier.scopus2-s2.0-84995403814
dc.identifier.startpage447
dc.identifier.urihttps://rdlopen.rawdatalibrary.net/r/ebyu/14896
dc.identifier.volume25
dc.identifier.wosWOS:000399338100028
dc.language.isoen
dc.publisherElsevier Taiwan LLC
dc.relation.ispartofJournal of Food and Drug Analysis
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectantioxidant activity
dc.subjectcisplatin
dc.subjecthistology
dc.subjectoleuropein
dc.subjectoxidative DNA damage
dc.subjectrenal damage
dc.subjectAnimals
dc.subjectDNA Damage
dc.subjectIridoids
dc.subjectKidney
dc.subjectOxidative Stress
dc.subjectRats
dc.subjectRats, Sprague-Dawley
dc.subject8 hydroxydeoxyguanosine
dc.subjectcreatinine
dc.subjectDNA
dc.subjectmalonaldehyde
dc.subjecturea
dc.subjecturic acid
dc.subjectiridoid
dc.subjectadult
dc.subjectanimal cell
dc.subjectanimal experiment
dc.subjectanimal model
dc.subjectanimal tissue
dc.subjectArticle
dc.subjectcontrolled study
dc.subjectcreatinine blood level
dc.subjectDNA determination
dc.subjectdrug mechanism
dc.titleEffect of oleuropein against chemotherapy drug-induced histological changes, oxidative stress, and DNA damages in rat kidney injury
dc.typeArticle
dspace.entity.typePublication
rdl.citation.scopus63
rdl.citation.wos56
rdl.departmentDepartment of Biology, Erzincan University, Uzumlu Vocational School, Erzincan, Turkey.
rdl.oa.statusgold
rdl.source.indexSCOPUS
rdl.source.indexWOS
rdl.source.indexPUBMED
rdl.wos.indexScience Citation Index Expanded (SCI-EXPANDED)