Carvone protects against paclitaxel-induced retinal and optic nerve cytotoxicity: a histopathological study

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Purpose: Carvone (CVN) is a natural monoterpene found in essential oils of many aromatic plant species. In this study, we investigated the protective effect of CVN against paclitaxel (PTX)-induced retinal and optic nerve cytotoxicity in rats. Methods: Twenty-four male adult Wistar albino rats (250–400 g) were randomized into four equal groups comprising six animals in each. Group 1 (control group) received intraperitoneal (i.p.) saline solution (0.5 mL/200 g) weekly for 4 weeks. Group 2 received i.p. CVN [(S)-(+)- CVN, (5S)-5-Isopropenyl-2-methyl-2-cyclohexen-1-one, C10H14, 25 mg/kg], while Group 3 received i.p. PTX (5 mg/kg) weekly for 4 weeks. Group 4 received i.p. CVN (25 mg/kg) 30 min after i.p. PTX (5 mg/kg) weekly for 4 weeks. At the end of the experimental period, retinal and optic nerve tissues were evaluated histopathologically. Results: All retinal specimens in control and CVN groups were histopathologically normal. In PTX group all eyes (6/6) demonstrated increased retinal vascularity and rosette-like structures in the outer nuclear layer, while in PTX-CVN group all eyes (6/6) demonstrated normal retinal vascularity and absence of rosette-like structures. All optic nerve specimens in control and CVN groups were histopathologically normal. In PTX group all eyes (6/6) demonstrated severe vacuolization and decrease in the number of astrocytes and oligodendrocytes, while 3 eyes (3/6) demonstrated marked single cell necrosis. In PTX-CVN group, 4 eyes (4/6) demonstrated moderate vacuolization while, 2 eyes (2/6) had none. Compared with PTX group, 1 eye (1/6) in PTX-CVN group demonstrated a decrease in numbers of astrocytes and oligodendrocytes while 5 eyes (5/6) were normal. No remarkable single cell necrosis was observed in PTX-CVN group. Conclusions: Our histopathological findings demonstrated the potential protective role of CVN against PTX-induced retinal and optic nerve cytotoxicity. CVN might be a promising molecule in counteracting oxidative stress-based cytotoxicity in the field of retinal and optic nerve disorders. © 2019, © 2019 Informa UK Limited, trading as Taylor & Francis Group.

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AlanDeğerDil
dc.contributor.authorCinici, Emine
dc.contributor.authorDilekmen, Nilay
dc.contributor.authorKutlu, Zerrin
dc.contributor.authorDincer, Busra
dc.contributor.authorCinici, Ozkan
dc.contributor.authorBalta, Hilal
dc.contributor.authorCalık, Ilknur
dc.date.accessioned2026-10-18T20:28:28.341233348Z
dc.date.available2026-10-18T20:28:28.341233348Z
dc.date.issued2019
dc.description.abstractPurpose: Carvone (CVN) is a natural monoterpene found in essential oils of many aromatic plant species. In this study, we investigated the protective effect of CVN against paclitaxel (PTX)-induced retinal and optic nerve cytotoxicity in rats. Methods: Twenty-four male adult Wistar albino rats (250–400 g) were randomized into four equal groups comprising six animals in each. Group 1 (control group) received intraperitoneal (i.p.) saline solution (0.5 mL/200 g) weekly for 4 weeks. Group 2 received i.p. CVN [(S)-(+)- CVN, (5S)-5-Isopropenyl-2-methyl-2-cyclohexen-1-one, C10H14, 25 mg/kg], while Group 3 received i.p. PTX (5 mg/kg) weekly for 4 weeks. Group 4 received i.p. CVN (25 mg/kg) 30 min after i.p. PTX (5 mg/kg) weekly for 4 weeks. At the end of the experimental period, retinal and optic nerve tissues were evaluated histopathologically. Results: All retinal specimens in control and CVN groups were histopathologically normal. In PTX group all eyes (6/6) demonstrated increased retinal vascularity and rosette-like structures in the outer nuclear layer, while in PTX-CVN group all eyes (6/6) demonstrated normal retinal vascularity and absence of rosette-like structures. All optic nerve specimens in control and CVN groups were histopathologically normal. In PTX group all eyes (6/6) demonstrated severe vacuolization and decrease in the number of astrocytes and oligodendrocytes, while 3 eyes (3/6) demonstrated marked single cell necrosis. In PTX-CVN group, 4 eyes (4/6) demonstrated moderate vacuolization while, 2 eyes (2/6) had none. Compared with PTX group, 1 eye (1/6) in PTX-CVN group demonstrated a decrease in numbers of astrocytes and oligodendrocytes while 5 eyes (5/6) were normal. No remarkable single cell necrosis was observed in PTX-CVN group. Conclusions: Our histopathological findings demonstrated the potential protective role of CVN against PTX-induced retinal and optic nerve cytotoxicity. CVN might be a promising molecule in counteracting oxidative stress-based cytotoxicity in the field of retinal and optic nerve disorders. © 2019, © 2019 Informa UK Limited, trading as Taylor & Francis Group.
dc.identifier.doi10.1080/15569527.2019.1608229
dc.identifier.eissn1556-9535
dc.identifier.endpage293
dc.identifier.issn1556-9527
dc.identifier.issue3
dc.identifier.pmid31010341
dc.identifier.scopus2-s2.0-85066055766
dc.identifier.startpage290
dc.identifier.urihttps://rdlopen.rawdatalibrary.net/r/ebyu/13638
dc.identifier.volume38
dc.identifier.wosWOS:000469732600001
dc.language.isoen
dc.publisherTaylor and Francis Ltd
dc.relation.ispartofCutaneous and Ocular Toxicology
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectantioxidant
dc.subjectcarvone
dc.subjectcytotoxicity
dc.subjectoxidative stress
dc.subjectPaclitaxel
dc.subjectAnimals
dc.subjectAntineoplastic Agents, Phytogenic
dc.subjectCyclohexane Monoterpenes
dc.subjectMale
dc.subjectOptic Nerve
dc.subjectProtective Agents
dc.subjectRats, Wistar
dc.subjectRetina
dc.subjectsodium chloride
dc.subjectantineoplastic agent
dc.subjectprotective agent
dc.subjectadult
dc.subjectanimal experiment
dc.subjectanimal tissue
dc.subjectArticle
dc.subjectastrocyte
dc.subjectcell death
dc.subjectcell vacuole
dc.subjectcontrolled study
dc.subjecteye protection
dc.subjecteye toxicity
dc.subjecthistopathology
dc.subjectnonhuman
dc.subjectoligodendroglia
dc.subjectrat
dc.titleCarvone protects against paclitaxel-induced retinal and optic nerve cytotoxicity: a histopathological study
dc.typeArticle
dspace.entity.typePublication
rdl.citation.scopus9
rdl.citation.wos8
rdl.source.indexSCOPUS
rdl.source.indexWOS
rdl.wos.indexScience Citation Index Expanded (SCI-EXPANDED)