Oleuropein Ameliorates Cisplatin-induced Hematological Damages Via Restraining Oxidative Stress and DNA Injury

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The prevalence of cancer, in the world is increasing steadily. Despite intense research efforts, no approved therapy is yet available. Cisplatin is a chemotherapeutic drug but induces acute tissue injury. Oleuropein (OLE) is a major phenolic compound and used as a possible natural antioxidant, antimicrobial, and anticancer agent. We hypothesized that antioxidant activity of OLE may decrease cisplatin-induced oxidative stress and prevent to the development of chemotherapeutic complications including abnormality in hematological condition. Male Sprague Dawley rats were used in the experiments. Rats were randomly assigned to one of eight groups: control group; group treated with i.p. injection in a single dose of 7 mg/kg/day cisplatin; groups treated with 50, 100 and 200 mg/kg/day OLE (i.p.); and groups treated with OLE for 3 days starting at 24 h following cisplatin injection. First, hematological assessment was appreciated between control and experimental groups. Second, total oxidative stress (TOS) and total antioxidant capacity (TAC) levels of blood were measured by biochemical studies. In addition to this, oxidative DNA damage was determined by measuring as increases in 8-hydroxy-deoxyguanosine (8-OH-dG) adducts. The treatment with cisplatin elevated the TOS and 8-OH-dG levels that were then reversed by OLE. Reductions in antioxidant capacity with respect to corresponding controls were also restored by OLE treatment. These findings suggest that the OLE treatment against cisplatin-induced toxicity improves the function of blood cells and helps them to survive in the belligerent environment created by free radicals. © 2016, Indian Society of Haematology & Transfusion Medicine.

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RDL Kalıcı Bağlantı (PID)
https://rdlopen.rawdatalibrary.net/r/ebyu/14584Resmi atıflarda kullanılan kalıcı adres
DOI
https://doi.org/10.1007/s12288-016-0718-3Yayıncı resmi DOI adresi
Tam Kayıt
AlanDeğerDil
dc.contributor.authorGeyikoğlu, Fatime
dc.contributor.authorÇolak, Suat
dc.contributor.authorTürkez, Hasan
dc.contributor.authorBakır, Murat
dc.contributor.authorKoç, Kübra
dc.contributor.authorHosseinigouzdagani, Mir Khalil
dc.contributor.authorÇeriğ, Salim
dc.contributor.authorSönmez, Merve
dc.date.accessioned2026-10-18T20:29:23.292911561Z
dc.date.available2026-10-18T20:29:23.292911561Z
dc.date.issued2017
dc.description.abstractThe prevalence of cancer, in the world is increasing steadily. Despite intense research efforts, no approved therapy is yet available. Cisplatin is a chemotherapeutic drug but induces acute tissue injury. Oleuropein (OLE) is a major phenolic compound and used as a possible natural antioxidant, antimicrobial, and anticancer agent. We hypothesized that antioxidant activity of OLE may decrease cisplatin-induced oxidative stress and prevent to the development of chemotherapeutic complications including abnormality in hematological condition. Male Sprague Dawley rats were used in the experiments. Rats were randomly assigned to one of eight groups: control group; group treated with i.p. injection in a single dose of 7 mg/kg/day cisplatin; groups treated with 50, 100 and 200 mg/kg/day OLE (i.p.); and groups treated with OLE for 3 days starting at 24 h following cisplatin injection. First, hematological assessment was appreciated between control and experimental groups. Second, total oxidative stress (TOS) and total antioxidant capacity (TAC) levels of blood were measured by biochemical studies. In addition to this, oxidative DNA damage was determined by measuring as increases in 8-hydroxy-deoxyguanosine (8-OH-dG) adducts. The treatment with cisplatin elevated the TOS and 8-OH-dG levels that were then reversed by OLE. Reductions in antioxidant capacity with respect to corresponding controls were also restored by OLE treatment. These findings suggest that the OLE treatment against cisplatin-induced toxicity improves the function of blood cells and helps them to survive in the belligerent environment created by free radicals. © 2016, Indian Society of Haematology & Transfusion Medicine.
dc.description.sponsorshipThis study was funded by Atatürk University (Grant Number: BAP- 2015/94).
dc.identifier.doi10.1007/s12288-016-0718-3
dc.identifier.eissn0974-0449
dc.identifier.endpage354
dc.identifier.issn0971-4502
dc.identifier.issue3
dc.identifier.pmcidPMC5544628
dc.identifier.pmid28824236
dc.identifier.scopus2-s2.0-84982124859
dc.identifier.startpage348
dc.identifier.urihttps://rdlopen.rawdatalibrary.net/r/ebyu/14584
dc.identifier.volume33
dc.identifier.wosWOS:000407326300008
dc.language.isoen
dc.publisherSpringer India
dc.relation.ispartofIndian Journal of Hematology and Blood Transfusion
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectCisplatin
dc.subjectDNA damage
dc.subjectHematological parameters
dc.subjectOleuropein
dc.subjectOxidative stress
dc.subjectTotal antioxidant capacity
dc.subject8 hydroxydeoxyguanosine
dc.subjecthemoglobin
dc.subjecthydrogen peroxide
dc.subjecttrolox C
dc.subjectanimal cell
dc.subjectanimal experiment
dc.subjectanimal model
dc.subjectantioxidant activity
dc.subjectantioxidant assay
dc.subjectArticle
dc.subjectbasophil
dc.subjectblood toxicity
dc.subjectcontrolled study
dc.subjecteosinophil
dc.subjecthematocrit
dc.subjecthemoglobin blood level
dc.subjectleukocyte differential count
dc.subjectlymphocyte
dc.subjectmean corpuscular hemoglobin
dc.subjectmean corpuscular volume
dc.subjectmonocyte
dc.subjectneutrophil
dc.subjectnonhuman
dc.subjectrat
dc.titleOleuropein Ameliorates Cisplatin-induced Hematological Damages Via Restraining Oxidative Stress and DNA Injury
dc.typeArticle
dspace.entity.typePublication
rdl.citation.scopus15
rdl.citation.wos14
rdl.departmentÜzümlü Vocational School, Erzincan University, Erzincan, Turkey. | Department of Biology, Faculty of Art and Science, Erzincan University, Erzincan, Turkey.
rdl.oa.statusgreen
rdl.source.indexSCOPUS
rdl.source.indexWOS
rdl.source.indexPUBMED
rdl.wos.indexScience Citation Index Expanded (SCI-EXPANDED)