Comparative effects of topical Maresin-1 and cyclosporine A in a capsaicin-induced rat model of neurotrophic keratopathy

dc.contributor.authorSezis, Selen Canan
dc.contributor.authorKobat, Sabiha Gungor
dc.contributor.authorKuloglu, Tuncay
dc.contributor.authorIlhan, Nevin
dc.contributor.authorErten, Fusun
dc.date.accessioned2026-09-08T07:13:35Z
dc.date.issued2026
dc.departmentFırat Üniveristesi
dc.description.abstractPurpose: To evaluate and compare the effects of topical Maresin-1 (MaR1) and cyclosporine A (CsA) in a capsaicin-induced rat model of neurotrophic keratopathy (NK). Methods: A total of 40 Sprague-Dawley rats were allocated to five groups (n = 8 per group): Control, NK, NK + Vehicle, NK + CsA (0.05%), and NK + MaR1. Except for the Control group, all animals received a single subcutaneous injection of capsaicin (50 mg/kg) on postnatal day 2. Topical treatments were applied twice daily for 14 days. Corneal TrkA, TNF-alpha, and Caspase-3 expression were assessed by immunohistochemistry and Western blot. Results: Both treatment groups significantly restored TrkA expression and reduced TNF-alpha and Caspase-3 relative to NK + Vehicle (p < 0.05 for all). CsA produced greater suppression of TNF-alpha than MaR1 (p < 0.001), whereas MaR1 demonstrated greater reduction in Caspase-3 than CsA (p = 0.013), with no significant difference between groups for TrkA (p = 0.054). Conclusion: Both MaR1 and CsA significantly attenuated the neurotrophic, inflammatory, and apoptotic changes associated with experimental NK. The distinct efficacy profiles of the two agents suggest complementary mechanisms of action and warrant further investigation of MaR1 in neurotrophic keratopathy.
dc.description.sponsorshipFimath;rat University Scientific Research Projects Coordination Unit (FUBAP) [TF.25.30] -- This study was supported by the F & imath;rat University Scientific Research Projects Coordination Unit (FUBAP) as a thesis project under project number TF.25.30.
dc.identifier.doi10.1016/j.exer.2026.111193
dc.identifier.issn0014-4835
dc.identifier.issn1096-0007
dc.identifier.orcid0000-0002-7901-2498
dc.identifier.pmid42567396
dc.identifier.scopus2-s2.0-105047628990
dc.identifier.scopusqualityQ1
dc.identifier.urihttps://doi.org/10.1016/j.exer.2026.111193
dc.identifier.urihttps://hdl.handle.net/11508/65510
dc.identifier.volume272
dc.identifier.wosWOS:001854344700001
dc.identifier.wosqualityQ2
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.indekslendigikaynakPubMed
dc.language.isoen
dc.publisherAcademic Press Ltd- Elsevier Science Ltd
dc.relation.ispartofExperimental Eye Research
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.snmzKA_WOS_20250903
dc.subjectTissue Regeneration
dc.subjectCurrent Challenges
dc.subjectCorneal
dc.subjectExpression
dc.subjectMediator
dc.subjectDeath
dc.subjectCells
dc.titleComparative effects of topical Maresin-1 and cyclosporine A in a capsaicin-induced rat model of neurotrophic keratopathy
dc.typeArticle

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