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https://hdl.handle.net/11499/10610
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DC Field | Value | Language |
---|---|---|
dc.contributor.author | Kaya, Hüseyin | - |
dc.contributor.author | Pekel, G. | - |
dc.contributor.author | Yörükoğlu, A. | - |
dc.contributor.author | Hiraali, M.C. | - |
dc.contributor.author | Şahin, B. | - |
dc.date.accessioned | 2019-08-16T13:31:54Z | |
dc.date.available | 2019-08-16T13:31:54Z | |
dc.date.issued | 2018 | - |
dc.identifier.issn | 1542-233X | - |
dc.identifier.uri | https://hdl.handle.net/11499/10610 | - |
dc.identifier.uri | https://doi.org/10.1097/ICL.0000000000000512 | - |
dc.description.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. | en_US |
dc.language.iso | en | en_US |
dc.publisher | NLM (Medline) | en_US |
dc.relation.ispartof | Eye & contact lens | en_US |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.subject | 1,3 benzodioxole derivative | en_US |
dc.subject | angiogenesis inhibitor | en_US |
dc.subject | antioxidant | en_US |
dc.subject | bevacizumab | en_US |
dc.subject | phenol derivative | en_US |
dc.subject | sesamol | en_US |
dc.subject | animal | en_US |
dc.subject | combination drug therapy | en_US |
dc.subject | cornea neovascularization | en_US |
dc.subject | disease model | en_US |
dc.subject | intraocular drug administration | en_US |
dc.subject | rat | en_US |
dc.subject | topical drug administration | en_US |
dc.subject | Wistar rat | en_US |
dc.subject | Administration, Topical | en_US |
dc.subject | Angiogenesis Inhibitors | en_US |
dc.subject | Animals | en_US |
dc.subject | Antioxidants | en_US |
dc.subject | Benzodioxoles | en_US |
dc.subject | Bevacizumab | en_US |
dc.subject | Corneal Neovascularization | en_US |
dc.subject | Disease Models, Animal | en_US |
dc.subject | Drug Therapy, Combination | en_US |
dc.subject | Injections, Intraocular | en_US |
dc.subject | Phenols | en_US |
dc.subject | Rats | en_US |
dc.subject | Rats, Wistar | en_US |
dc.title | Is Sesamol Effective in Corneal Neovascularization? | en_US |
dc.type | Article | en_US |
dc.identifier.volume | 44 | en_US |
dc.identifier.startpage | S414 | |
dc.identifier.startpage | S414 | en_US |
dc.identifier.endpage | S419 | en_US |
dc.identifier.doi | 10.1097/ICL.0000000000000512 | - |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.identifier.pmid | 29944496 | en_US |
dc.identifier.scopus | 2-s2.0-85055777137 | en_US |
dc.identifier.wos | WOS:000457840400072 | en_US |
dc.identifier.scopusquality | Q2 | - |
dc.owner | Pamukkale University | - |
item.openairecristype | http://purl.org/coar/resource_type/c_18cf | - |
item.openairetype | Article | - |
item.cerifentitytype | Publications | - |
item.fulltext | No Fulltext | - |
item.grantfulltext | none | - |
item.languageiso639-1 | en | - |
crisitem.author.dept | 14.01. Surgical Medicine | - |
crisitem.author.dept | 14.01. Surgical Medicine | - |
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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