Effect of topical motesanib in experimental corneal neovascularization model

dc.contributor.authorCelenk, Mukaddes
dc.contributor.authorYildirim, Hakan
dc.contributor.authorTektemur, Ahmet
dc.contributor.authorBalbaba, Mehmet
dc.contributor.authorErdag, Murat
dc.date.accessioned2026-08-12T17:20:47Z
dc.date.issued2023
dc.departmentFırat Üniversitesi
dc.description.abstractPurposeThis study aimed to compare the efficacy of topical bevacizumab and motesanib in an experimental corneal neovascularization model, and find the most effective motesanib dose.Materials and methodsIn experiments, 42 Wistar Albino rats were randomly divided into six groups (n = 7). Corneal cauterization was applied to all groups except the group 1. Group 1 did not receive any treatment. Topical dimethylsulfoxide was applied to sham group three times a day(tid). Topical bevacizumab drops (5 mg/ml) were applied to Group 3 tid. Topical motesanib drops with a dose of 2.5, 5, and 7.5 mg/ml were respectively applied in Groups 4, 5, and 6 tid. On the 8th day, corneal photographs of all rats were taken under general anesthesia, and the percentage of corneal neovascular area was calculated. VEGF-A mRNA, VEGFR-2 mRNA, miRNA-21, miRNA-27a, miRNA-31, miRNA-126, miRNA-184, and miRNA-204 were evaluated by the qRT-PCR method in corneas taken after decapitation.ResultsThe percentage of corneal neovascularization areas and VEGF-A mRNA expression levels were decreased in all treatment groups compared to group 2 (p < 0.05). VEGFR-2 mRNA levels were found to be statistically significantly decreased in groups 4 and 6 compared to group 2 (p < 0.05). Statistically significant changes were detected in the expression levels of only miRNA-126 among all miRNAs.ConclusionMotesanib with a dose of 7.5 mg/ml statistically significantly suppressed the VEGFR-2 mRNA level compared with other treatment doses and may be more effective than bevacizumab. Further, miRNA-126 can be used as a proangiogenic marker.
dc.description.sponsorshipFirat University Scientific Research Project Center (FUBAP) [TF: 2021/028]
dc.description.sponsorshipFinancial support was received from Firat University Scientific Research Project Center (FUBAP) for this sub-mission (Project no: TF: 2021/028).
dc.identifier.doi10.1007/s10792-023-02685-3
dc.identifier.endpage2997
dc.identifier.issn0165-5701
dc.identifier.issn1573-2630
dc.identifier.issue8
dc.identifier.orcid0000-0001-6951-8260
dc.identifier.orcid0000-0001-8857-994X
dc.identifier.pmid36971928
dc.identifier.scopus2-s2.0-85150976860
dc.identifier.scopusqualityQ2
dc.identifier.startpage2989
dc.identifier.urihttps://doi.org/10.1007/s10792-023-02685-3
dc.identifier.urihttps://hdl.handle.net/11508/53694
dc.identifier.volume43
dc.identifier.wosWOS:000956695200003
dc.identifier.wosqualityQ3
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.indekslendigikaynakPubMed
dc.language.isoen
dc.publisherSpringer
dc.relation.ispartofInternational Ophthalmology
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.snmzKA_WoS_20260511
dc.subjectCorneal neovascularization
dc.subjectBevacizumab
dc.subjectMotesanib
dc.subjectQuantitative real-time polymerase chain reaction (qRT-PCR)
dc.titleEffect of topical motesanib in experimental corneal neovascularization model
dc.typeReview Article

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