Effect of Dasatinib on Oxidative Stress and Neovascularization in Experimental Corneal Neovascularization

dc.contributor.authorYildirim, Hakan
dc.contributor.authorBalbaba, Mehmet
dc.contributor.authorCanleblebici, Mehmet
dc.contributor.authorDal, Ali
dc.contributor.authorErdag, Murat
dc.contributor.authorIlhan, Nevin
dc.contributor.authorAkdeniz Incili, Canan
dc.date.accessioned2026-08-12T17:27:08Z
dc.date.issued2025
dc.departmentFırat Üniversitesi
dc.description.abstractPurpose: To compare the effects of topical bevacizumab and dasatinib on experimental corneal neovascularization and oxidative stress and to determine the effective dose of dasatinib. Methods: Forty-two healthy Wistar-Albino rats were randomly divided into six groups. The right corneas of all rats except group 1 were cauterized with silver nitrate. Group 2 received dimethyl sulfoxide, group 3 received topical bevacizumab (5 mg/mL, three times a day), and groups 4, 5, and 6 received dasatinib (2.5 mg/dL, 5 mg/dL, and 10 mg/dL, three times a day respectively), between days 1 and 7. The corneas were removed to determine the level of vascular endothelial growth factor (VEGF), platelet-derived growth factor (PDGF) values for neovascularization and superoxide dismutase (SOD), malondialdehyde (MDA), and protein carbonyl (PC) levels for analyzing oxidative stress. Nonparametric variance analysis and post hoc Tamhane test was used for statistical analysis. Results: The VEGF level was statistically significantly lower in groups 3, 4, and 5 compared with group 2 (P < 0.05). The PDGF, SOD and MDA levels were compared; there was significant difference between all the groups compared with group 2. However, the MDA level for group 6, compared with other treatment groups, had a higher value (P < 0.05). The PC levels compared were statistically significantly lower in groups 3 and 4 compared with group 2 (P < 0.05). Conclusions: Dasatinib 2.5 mg/dL was as effective as bevacizumab and seems to be dose-dependent and higher doses than 2.5 mg/dL show higher oxidative stress and an increase in neovascularization.
dc.identifier.doi10.1177/10807683251370551
dc.identifier.endpage589
dc.identifier.issn1080-7683
dc.identifier.issn1557-7732
dc.identifier.issue10
dc.identifier.orcid0000-0002-0208-8929
dc.identifier.orcid0000-0002-6554-8021
dc.identifier.pmid40838941
dc.identifier.scopus2-s2.0-105014143764
dc.identifier.scopusqualityQ2
dc.identifier.startpage582
dc.identifier.urihttps://doi.org/10.1177/10807683251370551
dc.identifier.urihttps://hdl.handle.net/11508/55087
dc.identifier.volume41
dc.identifier.wosWOS:001555096300001
dc.identifier.wosqualityQ2
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.indekslendigikaynakPubMed
dc.language.isoen
dc.publisherMary Ann Liebert, Inc
dc.relation.ispartofJournal of Ocular Pharmacology and Therapeutics
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.snmzKA_WoS_20260511
dc.subjectcorneal neovascularization
dc.subjectdasatinib
dc.subjectbevacizumab
dc.subjectoxidative stress
dc.titleEffect of Dasatinib on Oxidative Stress and Neovascularization in Experimental Corneal Neovascularization
dc.typeArticle

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