Effect of pycnogenol on ethanol-related oxidative retinal injury: an experimental study

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OBJECTIVE: We aimed at determining the protective effects of Pycnogenol on ethanol-induced retinotoxicity in an experimental model. MATERIALS AND METHODS: 30 male Wistar albino rats were randomly divided into three groups: an untreated healthy control (HC group), a group in which only ethanol was daily administered for six weeks (EtOH group), and a group in which ethanol + 40 mg/kg Pycnogenol was daily administered orally for six weeks (PEtOH group). The same volume (0.5 ml) of distilled water as solvent was applied in the same manner to the rats in the HC and EtOH groups. With the rats in the PEtOH and EtOH groups, 32% ethanol at a dose of 5 g/kg was administered by oral gavage one hour after the application of pycnogenol or distilled water. At the end of the experimental period, tissue samples were obtained for biochemical examination of malondialdehyde (MDA) and total glutathione (tGSH) levels, and afterwards, the eyes were removed for histopathological examination. RESULTS: Histopathological evaluations in the EtOH group showed significant destruction of retinal tissue with marked edema, decomposition and degeneration in layers, polymorphonuclear cell infiltration, dilatation and congestion in blood vessels. However, it was observed that MDA values increased and tGSH values decreased in the EtOH group. In the PEtOH group, MDA values decreased and GSH values increased. Again, degenerative changes were considerably less in this group. CONCLUSIONS: In the light of biochemical markers and histopathological evaluations, it was observed that ethanol exposure caused a significant degeneration in the retinal tissue. It was found that Pycnogenol administration significantly reduced the destructive effects seen histopathologically. Biochemical results also coincided with other findings. It was concluded that ethanol-induced rethytosis can be prevented to a large extent by Pycnogenol administration. © 2022 Verduci Editore s.r.l. All rights reserved.

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AlanDeğerDil
dc.contributor.authorYazici, G.N.
dc.contributor.authorSunar, M.
dc.contributor.authorSuleyman, B.
dc.contributor.authorAbdulkadir Çoban, T.
dc.contributor.authorKemal Arslan, Y.
dc.contributor.authorSuleyman, H.
dc.date.accessioned2026-10-18T20:27:49.988479887Z
dc.date.available2026-10-18T20:27:49.988479887Z
dc.date.issued2022
dc.description.abstractOBJECTIVE: We aimed at determining the protective effects of Pycnogenol on ethanol-induced retinotoxicity in an experimental model. MATERIALS AND METHODS: 30 male Wistar albino rats were randomly divided into three groups: an untreated healthy control (HC group), a group in which only ethanol was daily administered for six weeks (EtOH group), and a group in which ethanol + 40 mg/kg Pycnogenol was daily administered orally for six weeks (PEtOH group). The same volume (0.5 ml) of distilled water as solvent was applied in the same manner to the rats in the HC and EtOH groups. With the rats in the PEtOH and EtOH groups, 32% ethanol at a dose of 5 g/kg was administered by oral gavage one hour after the application of pycnogenol or distilled water. At the end of the experimental period, tissue samples were obtained for biochemical examination of malondialdehyde (MDA) and total glutathione (tGSH) levels, and afterwards, the eyes were removed for histopathological examination. RESULTS: Histopathological evaluations in the EtOH group showed significant destruction of retinal tissue with marked edema, decomposition and degeneration in layers, polymorphonuclear cell infiltration, dilatation and congestion in blood vessels. However, it was observed that MDA values increased and tGSH values decreased in the EtOH group. In the PEtOH group, MDA values decreased and GSH values increased. Again, degenerative changes were considerably less in this group. CONCLUSIONS: In the light of biochemical markers and histopathological evaluations, it was observed that ethanol exposure caused a significant degeneration in the retinal tissue. It was found that Pycnogenol administration significantly reduced the destructive effects seen histopathologically. Biochemical results also coincided with other findings. It was concluded that ethanol-induced rethytosis can be prevented to a large extent by Pycnogenol administration. © 2022 Verduci Editore s.r.l. All rights reserved.
dc.identifier.doi10.26355/eurrev_202207_29312
dc.identifier.endpage5232
dc.identifier.issn1128-3602
dc.identifier.issue14
dc.identifier.pmid35916821
dc.identifier.scopus2-s2.0-85135238183
dc.identifier.startpage5225
dc.identifier.urihttps://rdlopen.rawdatalibrary.net/r/ebyu/12978
dc.identifier.volume26
dc.identifier.wosWOS:000855680700010
dc.language.isoen
dc.publisherVerduci Editore s.r.l
dc.relation.ispartofEuropean Review for Medical and Pharmacological Sciences
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectEthanol
dc.subjectOxidative damage
dc.subjectPycnogenol
dc.subjectRetinotoxicity
dc.subjectAnimals
dc.subjectAntioxidants
dc.subjectFlavonoids
dc.subjectGlutathione
dc.subjectMale
dc.subjectOxidative Stress
dc.subjectPlant Extracts
dc.subjectRats
dc.subjectRats, Wistar
dc.subjectRetina
dc.subjectRetinal Diseases
dc.subjectWater
dc.subjectalcohol
dc.subjectdistilled water
dc.subjectmalonaldehyde
dc.subjectantioxidant
dc.subjectflavonoid
dc.subjectplant extract
dc.subjectpycnogenols
dc.subjectalbino rat
dc.subjectanimal experiment
dc.subjectanimal model
dc.subjectanimal tissue
dc.subjectArticle
dc.subjectbiochemistry
dc.subjectcell infiltration
dc.titleEffect of pycnogenol on ethanol-related oxidative retinal injury: an experimental study
dc.typeArticle
dspace.entity.typePublication
rdl.citation.scopus2
rdl.citation.wos3
rdl.departmentDepartment of Histology and Embryology, Department of Anatomy, Department of Pharmacology, Department of Biochemistry, Department of Biostatistics, Erzincan Binali Yıldırım University, School of Medicine, Erzincan, Turkey. gulcenazyazici.ank@gmail.com.
rdl.source.indexSCOPUS
rdl.source.indexWOS
rdl.source.indexPUBMED
rdl.wos.indexScience Citation Index Expanded (SCI-EXPANDED)