The effects of rutin on cisplatin induced oxidative retinal and optic nerve injury: an experimental study

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Aim: To determine the role of rutin in prevention of cisplatin induced retinal and optic nerve injury in an experimental study. Materials and methods: Totally 18 albino Wistar male rats were assigned into three groups, as follows: healthy controls (HC group), only cisplatin administered group for 14 days (CIS group), and rutin + cisplatin administered group for 14 days (RC group). Blood samples were obtained from animals just before the scarification. Serum malondialdehyde (MDA), myeloperoxidase (MPO), total glutathione (tGSH), superoxide dismutase (SOD), interleukin 1 beta (IL-1β) and tumour necrosis factor alpha (TNF-α) levels were investigated. The eyes were enucleated for histopathological evaluations of retina and optic nerve. Results: MDA, MPO, IL-1β and TNF-α levels were statistically significantly higher (p < 0.001) in CIS group compared with other two groups while tGSH and SOD levels were statistically significantly lower (p < 0.001). Regarding these parameters, in CIS group MDA, MPO, IL1β and TNF-α levels were statistically significantly increased with cisplatin administration and giving rutin concomitantly with cisplatin prevented this increase. On the other hand, tGSH and SOD levels were statistically significantly decreased with cisplatin administration and giving rutin concomitantly with cisplatin prevented this decrease. In qualitative analyses of histopathological findings of retina and optic nerve; the results of RC group were similar with the results of healthy controls; but there was statistically significant differences between CIS group and other two groups (p < 0.001). Conclusions: Concomitant rutin administration may prevent the detrimental effects of cisplatin on lipid peroxidation, oxidative stress and inflammation markers and may also avert the histopathological damage on retina and optic nerve. Further studies are warranted to determine the effects of cisplatin and rutin on eye. © 2018, © 2018 Informa UK Limited, trading as Taylor & Francis Group.

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AlanDeğerDil
dc.contributor.authorTaşlı, Nurdan Gamze
dc.contributor.authorUçak, Turgay
dc.contributor.authorKarakurt, Yücel
dc.contributor.authorKeskin Çimen, Ferda
dc.contributor.authorÖzbek Bilgin, Aslı
dc.contributor.authorKurt, Nezahat
dc.contributor.authorSüleyman, Halis
dc.date.accessioned2026-10-18T20:29:18.256059408Z
dc.date.available2026-10-18T20:29:18.256059408Z
dc.date.issued2018
dc.description.abstractAim: To determine the role of rutin in prevention of cisplatin induced retinal and optic nerve injury in an experimental study. Materials and methods: Totally 18 albino Wistar male rats were assigned into three groups, as follows: healthy controls (HC group), only cisplatin administered group for 14 days (CIS group), and rutin + cisplatin administered group for 14 days (RC group). Blood samples were obtained from animals just before the scarification. Serum malondialdehyde (MDA), myeloperoxidase (MPO), total glutathione (tGSH), superoxide dismutase (SOD), interleukin 1 beta (IL-1β) and tumour necrosis factor alpha (TNF-α) levels were investigated. The eyes were enucleated for histopathological evaluations of retina and optic nerve. Results: MDA, MPO, IL-1β and TNF-α levels were statistically significantly higher (p < 0.001) in CIS group compared with other two groups while tGSH and SOD levels were statistically significantly lower (p < 0.001). Regarding these parameters, in CIS group MDA, MPO, IL1β and TNF-α levels were statistically significantly increased with cisplatin administration and giving rutin concomitantly with cisplatin prevented this increase. On the other hand, tGSH and SOD levels were statistically significantly decreased with cisplatin administration and giving rutin concomitantly with cisplatin prevented this decrease. In qualitative analyses of histopathological findings of retina and optic nerve; the results of RC group were similar with the results of healthy controls; but there was statistically significant differences between CIS group and other two groups (p < 0.001). Conclusions: Concomitant rutin administration may prevent the detrimental effects of cisplatin on lipid peroxidation, oxidative stress and inflammation markers and may also avert the histopathological damage on retina and optic nerve. Further studies are warranted to determine the effects of cisplatin and rutin on eye. © 2018, © 2018 Informa UK Limited, trading as Taylor & Francis Group.
dc.identifier.doi10.1080/15569527.2018.1442842
dc.identifier.eissn1556-9535
dc.identifier.endpage257
dc.identifier.issn1556-9527
dc.identifier.issue3
dc.identifier.pmid29455557
dc.identifier.scopus2-s2.0-85044295999
dc.identifier.startpage252
dc.identifier.urihttps://rdlopen.rawdatalibrary.net/r/ebyu/14502
dc.identifier.volume37
dc.identifier.wosWOS:000438110100008
dc.language.isoen
dc.publisherTaylor and Francis Ltd
dc.relation.ispartofCutaneous and Ocular Toxicology
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectCisplatin
dc.subjectoptic nerve toxicity
dc.subjectretina toxicity
dc.subjectrutin
dc.subjectAnimals
dc.subjectAntineoplastic Agents
dc.subjectAntioxidants
dc.subjectBiomarkers
dc.subjectDisease Models, Animal
dc.subjectHumans
dc.subjectLipid Peroxidation
dc.subjectMale
dc.subjectOptic Nerve
dc.subjectOxidative Stress
dc.subjectRats
dc.subjectRats, Wistar
dc.subjectRetina
dc.subjectglutathione
dc.subjectinterleukin 1beta
dc.subjectmalonaldehyde
dc.subjectmyeloperoxidase
dc.subjectrutoside
dc.subjectsuperoxide dismutase
dc.subjecttumor necrosis factor
dc.subjectantineoplastic agent
dc.subjectantioxidant
dc.subjectbiological marker
dc.subjectanimal cell
dc.subjectanimal experiment
dc.subjectanimal model
dc.titleThe effects of rutin on cisplatin induced oxidative retinal and optic nerve injury: an experimental study
dc.typeArticle
dspace.entity.typePublication
rdl.citation.scopus28
rdl.citation.wos27
rdl.departmenta Department of Ophthalmology, College of Medicine , Erzincan University Hospital , Erzincan , Turkey. | b Department of Pathology, College of Medicine , Erzincan University Hospital , Erzincan , Turkey. | c Department of Pharmacology, College of Medicine , Erzincan University Hospital , Erzincan , Turkey.
rdl.source.indexSCOPUS
rdl.source.indexWOS
rdl.source.indexPUBMED
rdl.wos.indexScience Citation Index Expanded (SCI-EXPANDED)