The effects of lycopene on alloxan induced diabetic optic neuropathy

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Aim: To determine the effects of lycopene treatment in prevention of diabetes associated inflammatory response and oxidative stress in an experimental model. With this aim we investigated the levels of oxidative stress markers including Malondialdehyde (MDA), and total oxidative status (TOS)together with inflammatory markers including nuclear factor- kappa B (NFKB) and tumor necrosis factor α (TNF-α) and antioxidants including total glutathione (TGSH), total oxidative status (TOS) and total anti-oxidative status (TAS) levels on eye tissue. Material and methods: Totally 18 albino Wistar male rats (250–280 grams) assigned into three groups, with six rats in each group as follows: healthy group (HG), control group (CG), and lycopene group (LG). The diabetes was induced with alloxan administration in rats of CG and LG. Lycopene (4 mg/kg) was administered to the rats in LG once a day for 3 months. At the end of this period, the animals were sacrificed and their eyes were enucleated for histopathological evaluations. From the tissues, MDA, GSH, TOS, TAS, TNF-α and NF-κB levels were analyzed. Results: MDA, TOS, OSI, NFKB and TNF-α levels were significantly higher, while TGSH and TAS levels were significantly lower in CG compared with HG (p < 0.001). On the other hand in LG; MDA, TOS, OSI, NFKB and TNF-α levels were significantly lower, while TGSH and TAS levels were significantly higher compared with CG (p < 0.001). Regarding histopathological findings, although there was severe damage on optic nerve of rats in CG; there was only a slight damage in lycopene administered group. Conclusion: For the first time in literature we determined that, lycopene was significantly effective in prevention of augmented inflammation and oxidative stress on eye tissue associated with diabetes, as well as the tissue damage on optic nerve. However, studies investigating the long-term clinical effects of lycopene on diabetic individuals are warranted. © 2018, © 2018 Informa UK Limited, trading as Taylor & Francis Group.

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AlanDeğerDil
dc.contributor.authorIcel, Erel
dc.contributor.authorIcel, Aykut
dc.contributor.authorUçak, Turgay
dc.contributor.authorKarakurt, Yücel
dc.contributor.authorElpeze, Burcu
dc.contributor.authorKeskin Çimen, Ferda
dc.contributor.authorSüleyman, Halis
dc.date.accessioned2026-10-18T20:28:57.916918896Z
dc.date.available2026-10-18T20:28:57.916918896Z
dc.date.issued2019
dc.description.abstractAim: To determine the effects of lycopene treatment in prevention of diabetes associated inflammatory response and oxidative stress in an experimental model. With this aim we investigated the levels of oxidative stress markers including Malondialdehyde (MDA), and total oxidative status (TOS)together with inflammatory markers including nuclear factor- kappa B (NFKB) and tumor necrosis factor α (TNF-α) and antioxidants including total glutathione (TGSH), total oxidative status (TOS) and total anti-oxidative status (TAS) levels on eye tissue. Material and methods: Totally 18 albino Wistar male rats (250–280 grams) assigned into three groups, with six rats in each group as follows: healthy group (HG), control group (CG), and lycopene group (LG). The diabetes was induced with alloxan administration in rats of CG and LG. Lycopene (4 mg/kg) was administered to the rats in LG once a day for 3 months. At the end of this period, the animals were sacrificed and their eyes were enucleated for histopathological evaluations. From the tissues, MDA, GSH, TOS, TAS, TNF-α and NF-κB levels were analyzed. Results: MDA, TOS, OSI, NFKB and TNF-α levels were significantly higher, while TGSH and TAS levels were significantly lower in CG compared with HG (p < 0.001). On the other hand in LG; MDA, TOS, OSI, NFKB and TNF-α levels were significantly lower, while TGSH and TAS levels were significantly higher compared with CG (p < 0.001). Regarding histopathological findings, although there was severe damage on optic nerve of rats in CG; there was only a slight damage in lycopene administered group. Conclusion: For the first time in literature we determined that, lycopene was significantly effective in prevention of augmented inflammation and oxidative stress on eye tissue associated with diabetes, as well as the tissue damage on optic nerve. However, studies investigating the long-term clinical effects of lycopene on diabetic individuals are warranted. © 2018, © 2018 Informa UK Limited, trading as Taylor & Francis Group.
dc.identifier.doi10.1080/15569527.2018.1530258
dc.identifier.eissn1556-9535
dc.identifier.endpage92
dc.identifier.issn1556-9527
dc.identifier.issue1
dc.identifier.pmid30277087
dc.identifier.scopus2-s2.0-85057339194
dc.identifier.startpage88
dc.identifier.urihttps://rdlopen.rawdatalibrary.net/r/ebyu/14178
dc.identifier.volume38
dc.identifier.wosWOS:000457026400013
dc.language.isoen
dc.publisherTaylor and Francis Ltd
dc.relation.ispartofCutaneous and Ocular Toxicology
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectdiabetes
dc.subjectLycopene
dc.subjectoptic nerve
dc.subjectAlloxan
dc.subjectAnimals
dc.subjectAnti-Inflammatory Agents
dc.subjectAntioxidants
dc.subjectDiabetes Mellitus, Experimental
dc.subjectDiabetic Neuropathies
dc.subjectGlutathione
dc.subjectMale
dc.subjectMalondialdehyde
dc.subjectNF-kappa B
dc.subjectOptic Nerve Diseases
dc.subjectRats, Wistar
dc.subjectRetina
dc.subjectTumor Necrosis Factor-alpha
dc.subjectimmunoglobulin enhancer binding protein
dc.subjectmalonaldehyde
dc.subjecttumor necrosis factor
dc.subjectantiinflammatory agent
dc.subjectantioxidant
dc.subjectanimal experiment
dc.subjectanimal model
dc.subjectanimal tissue
dc.subjectArticle
dc.subjectcontrolled study
dc.subjectdiabetic neuropathy
dc.subjectdrug effect
dc.subjecteye tissue
dc.titleThe effects of lycopene on alloxan induced diabetic optic neuropathy
dc.typeArticle
dspace.entity.typePublication
rdl.citation.scopus34
rdl.citation.wos30
rdl.departmenta Department of Ophthalmology , Erzincan University Hospital, College of Medicine , Erzincan , Turkey. | b Department of Internal Medicine , Erzincan University Hospital, College of Medicine , Erzincan , Turkey. | c Department of Pathology , Erzincan University Hospital, College of Medicine , Erzincan , Turkey. | d Department of Pharmacology , Erzincan University Hospital, College of Medicine , Erzincan , Turkey.
rdl.source.indexSCOPUS
rdl.source.indexWOS
rdl.source.indexPUBMED
rdl.wos.indexScience Citation Index Expanded (SCI-EXPANDED)