Please use this identifier to cite or link to this item: https://hdl.handle.net/11499/10610
Title: Is Sesamol Effective in Corneal Neovascularization?
Authors: Kaya, Hüseyin
Pekel, G.
Yörükoğlu, A.
Hiraali, M.C.
Şahin, B.
Keywords: 1,3 benzodioxole derivative
angiogenesis inhibitor
antioxidant
bevacizumab
phenol derivative
sesamol
animal
combination drug therapy
cornea neovascularization
disease model
intraocular drug administration
rat
topical drug administration
Wistar rat
Administration, Topical
Angiogenesis Inhibitors
Animals
Antioxidants
Benzodioxoles
Bevacizumab
Corneal Neovascularization
Disease Models, Animal
Drug Therapy, Combination
Injections, Intraocular
Phenols
Rats
Rats, Wistar
Publisher: NLM (Medline)
Abstract: OBJECTIVES: To evaluate the effects of topically and subconjunctivally administered sesamol on experimentally induced corneal neovascularization in rats. METHODS: Fifty-six right eyes of 56 Wistar Albino rats were chemically cauterized to induce corneal neovascularization in this experimental and comparative study. The subjects were divided into eight groups: topical sesamol (group 1), subconjunctival sesamol (group 2), topical bevacizumab (group 3), subconjunctival bevacizumab (group 4), topical bevacizumab+ sesamol (group 5), subconjunctival bevacizumab+ sesamol (group 6), topical Tween 80 (group 7), and control (group 8). The amount of subconjunctivally injected sesamol and bevacizumab was 1.25 mg each. Topical groups were administered 10 mg/mL drops twice daily. The control group was left untreated. To evaluate the degree of corneal neovascularization, digital photographs and corneal sections stained with hematoxylin-eosin and CD31 were used. RESULTS: When photographs of neovascularization areas were examined, all treatment groups showed statistically significant differences when compared with the control group (P<0.001). Topical sesamol was found to be more effective when compared with subconjunctival sesamol (P=0.003). Topical sesamol+ bevacizumab was found to be more effective when compared with topical bevacizumab (P=0.018). The numbers of new corneal vessels were as follows: 12.28±6.29 in group 1, 36.85±12.8 in group 2, 18.85±7.71 in group 3, 16.85±8.70 in group 4, 19.57±8.56 in group 5, 22.57±7.43 in group 6, 45.00±11.29 in group 7, and 51.16±5.91 in group 8 (P<0.001). CONCLUSIONS: The outcomes of this study suggest antiangiogenic effects of sesamol. The use of topical sesamol monotherapy or sesamol combined with bevacizumab may be options for the prevention of corneal neovascularization.
URI: https://hdl.handle.net/11499/10610
https://doi.org/10.1097/ICL.0000000000000512
ISSN: 1542-233X
Appears in Collections:PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection
Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
Tıp Fakültesi Koleksiyonu
WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection

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