Chemoprotective effects of curcumin on doxorubicin-induced nephrotoxicity in wistar rats: by modulating inflammatory cytokines, apoptosis, oxidative stress and oxidative DNA damage

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Özet

Doxorubicin (DXR) is one of the most important chemotherapeutic agent. However, nephrotoxicity reduces its clinical utility in humans. The aim of the study was to investigate protective effects of curcumin (CMN) against DXR-induced nephrotoxicity. Rats were subjected to oral treatment of CMN (100 and 200 mg/kg body weight) for 7 days. Nephrotoxicity was induced by single intra peritoneal injection of DXR (40 mg/kg body weight) on the fifth day and then the experiment was terminated on the eighth day. Nephroprotective effects of CMN were associated with decrease in serum toxicity markers and increase in antioxidant enzyme activities. CMN was able to reduced the levels of inflammatory markers such as TNF-α, NF-κB, IL-1β, iNOS and COX-2 in the rats. It also reduced the expressions of apoptotic marker including caspase-3, and oxidative DNA damage marker including 8-OHdG. Collectively, these findings indicated that CMN protect against DXR-induced nephrotoxicity.

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OpenAlex
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Tam Kayıt
AlanDeğerDil
dc.contributor.authorBenzer, Fulya
dc.contributor.authorKandemir, Fatih Mehmet
dc.contributor.authorKucukler, Sefa
dc.contributor.authorComaklı, Selim
dc.contributor.authorCaglayan, Cuneyt
dc.date.accessioned2026-10-28T14:56:40.418738379Z
dc.date.available2026-10-28T14:56:40.418738379Z
dc.date.issued2018
dc.description.abstractDoxorubicin (DXR) is one of the most important chemotherapeutic agent. However, nephrotoxicity reduces its clinical utility in humans. The aim of the study was to investigate protective effects of curcumin (CMN) against DXR-induced nephrotoxicity. Rats were subjected to oral treatment of CMN (100 and 200 mg/kg body weight) for 7 days. Nephrotoxicity was induced by single intra peritoneal injection of DXR (40 mg/kg body weight) on the fifth day and then the experiment was terminated on the eighth day. Nephroprotective effects of CMN were associated with decrease in serum toxicity markers and increase in antioxidant enzyme activities. CMN was able to reduced the levels of inflammatory markers such as TNF-α, NF-κB, IL-1β, iNOS and COX-2 in the rats. It also reduced the expressions of apoptotic marker including caspase-3, and oxidative DNA damage marker including 8-OHdG. Collectively, these findings indicated that CMN protect against DXR-induced nephrotoxicity.
dc.description.sponsorshipMunzur University, (YLTUB016–01)
dc.identifier.doi10.1080/13813455.2017.1422766
dc.identifier.eissn1744-4160
dc.identifier.endpage457
dc.identifier.issn1381-3455
dc.identifier.issue5
dc.identifier.pmid29302997
dc.identifier.scopus2-s2.0-85040971802
dc.identifier.startpage448
dc.identifier.urihttps://rdlopen.rawdatalibrary.net/r/munzur/3463
dc.identifier.volume124
dc.identifier.wosWOS:000447305900011
dc.language.isoen
dc.publisherTaylor and Francis Ltd
dc.relation.ispartofArchives of Physiology and Biochemistry
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectApoptosis
dc.subjectcurcumin
dc.subjectdoxorubicin
dc.subjectinflammation
dc.subjectnephrotoxicity
dc.subject.classificationBiochemistry & Molecular Biology
dc.subject.classificationBiophysics
dc.subject.classificationEndocrinology & Metabolism
dc.subject.classificationPhysiology
dc.subject.otherAnimals
dc.subject.otherAnti-Inflammatory Agents, Non-Steroidal
dc.subject.otherAntibiotics, Antineoplastic
dc.subject.otherAntioxidants
dc.subject.otherApoptosis
dc.subject.otherBiomarkers
dc.subject.otherCurcumin
dc.subject.otherCyclooxygenase 2
dc.subject.otherDNA Damage
dc.subject.otherDose-Response Relationship, Drug
dc.subject.otherDoxorubicin
dc.subject.otherKidney
dc.subject.otherLipid Peroxidation
dc.subject.otherMale
dc.subject.otherNitric Oxide Synthase Type II
dc.subject.otherOxidation-Reduction
dc.subject.otherOxidative Stress
dc.subject.otherProtective Agents
dc.subject.otherRandom Allocation
dc.subject.otherRats, Wistar
dc.subject.otherRenal Insufficiency
dc.subject.otherTopoisomerase II Inhibitors
dc.subject.otherantineoplastic antibiotic
dc.subject.otherantioxidant
dc.subject.otherbiological marker
dc.subject.othergyrase inhibitor
dc.subject.otherinducible nitric oxide synthase
dc.subject.othernonsteroid antiinflammatory agent
dc.subject.otherNos2 protein, rat
dc.subject.otherprotective agent
dc.subject.otherPtgs2 protein, rat
dc.subject.otheranimal
dc.subject.otherantagonists and inhibitors
dc.subject.otherblood
dc.subject.otherchemically induced
dc.subject.otherchemistry
dc.subject.otherdose response
dc.subject.otherdrug effect
dc.subject.otherimmunology
dc.subject.otherkidney failure
dc.subject.othermetabolism
dc.subject.otheroxidation reduction reaction
dc.subject.otherpathology
dc.subject.otherrandomization
dc.subject.otherWistar rat
dc.titleChemoprotective effects of curcumin on doxorubicin-induced nephrotoxicity in wistar rats: by modulating inflammatory cytokines, apoptosis, oxidative stress and oxidative DNA damage
dc.typeArticle
rdl.citation.openalex122
rdl.citation.scopus116
rdl.citation.wos111
rdl.departmenta Department of Food Engineering, Faculty of Engineering , Munzur University , Tunceli , Turkey
rdl.departmentb Department of Biochemistry, Faculty of Veterinary Medicine , Ataturk University , Erzurum , Turkey
rdl.departmentc Department of Pathology, Faculty of Veterinary Medicine , Ataturk University , Erzurum , Turkey
rdl.departmentd Department of Biochemistry, Faculty of Veterinary Medicine , Bingol University , Bingol , Turkey
rdl.oa.statusclosed
rdl.scopus.quartileQ2
rdl.sdgSDG03
rdl.source.indexSCOPUS
rdl.source.indexWOS
rdl.source.indexPUBMED
rdl.wos.indexScience Citation Index Expanded (SCI-EXPANDED)