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

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Özet

Purpose: 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-α, and Caspase-3 expression were assessed by immunohistochemistry and Western blot. Results: Both treatment groups significantly restored TrkA expression and reduced TNF-α and Caspase-3 relative to NK + Vehicle (p < 0.05 for all). CsA produced greater suppression of TNF-α 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.

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https://rdlopen.rawdatalibrary.net/r/munzur/1287Resmi atıflarda kullanılan kalıcı adres
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https://doi.org/10.1016/j.exer.2026.111193Yayıncı resmi DOI adresi
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AlanDeğerDil
dc.contributor.authorCanan Sezis, Selen
dc.contributor.authorGüngör Kobat, Sabiha
dc.contributor.authorKuloğlu, Tuncay
dc.contributor.authorİlhan, Nevin
dc.contributor.authorErten, Füsun
dc.date.accessioned2026-10-28T14:54:03.807524234Z
dc.date.available2026-10-28T14:54:03.807524234Z
dc.date.issued2026
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-α, and Caspase-3 expression were assessed by immunohistochemistry and Western blot. Results: Both treatment groups significantly restored TrkA expression and reduced TNF-α and Caspase-3 relative to NK + Vehicle (p < 0.05 for all). CsA produced greater suppression of TNF-α 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.sponsorshipFirat Üniversitesi, FU, (TF . 25 . 30 .)
dc.description.sponsorshipFirat Üniversitesi, FU
dc.identifier.articlenumber111193
dc.identifier.doi10.1016/j.exer.2026.111193
dc.identifier.eissn1096-0007
dc.identifier.issn0014-4835
dc.identifier.pmid42567396
dc.identifier.scopus2-s2.0-105047628990
dc.identifier.urihttps://rdlopen.rawdatalibrary.net/r/munzur/1287
dc.identifier.volume272
dc.identifier.wosWOS:001854344700001
dc.language.isoen
dc.publisherAcademic Press
dc.relation.ispartofExperimental Eye Research
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subject.classificationOphthalmology
dc.subject.otherAdministration, Topical
dc.subject.otherAnimals
dc.subject.otherApoptosis
dc.subject.otherBlotting, Western
dc.subject.otherCapsaicin
dc.subject.otherCaspase 3
dc.subject.otherCornea
dc.subject.otherCorneal Diseases
dc.subject.otherCranial Nerve Diseases
dc.subject.otherCyclosporine
dc.subject.otherDisease Models, Animal
dc.subject.otherDocosahexaenoic Acids
dc.subject.otherImmunosuppressive Agents
dc.subject.otherRats
dc.subject.otherRats, Sprague-Dawley
dc.subject.otherReceptor, trkA
dc.subject.otherSpecialized Pro-Resolving Mediators
dc.subject.otherTumor Necrosis Factor-alpha
dc.subject.othermaresin 1
dc.subject.otherprotein tyrosine kinase A
dc.subject.othertumor necrosis factor
dc.subject.other7,14-dihydroxydocosa-4,8,10,12,16,19-hexaenoic acid
dc.subject.otherdocosahexaenoic acid
dc.subject.otherimmunosuppressive agent
dc.subject.otherspecialized pro-resolving mediator
dc.subject.otheranimal experiment
dc.subject.otheranimal model
dc.subject.otheranimal tissue
dc.subject.otherArticle
dc.subject.othercapsaicin-induced experimental disease
dc.subject.othercontrolled study
dc.subject.othercornea tissue
dc.subject.otherfemale
dc.subject.otherimmunohistochemistry
dc.subject.otherimmunoreactivity
dc.subject.otherneurotrophic keratopathy
dc.subject.othernewborn
dc.subject.othernonhuman
dc.subject.otherplots and curves
dc.subject.otherprotein expression
dc.subject.otherprotein expression level
dc.subject.otherrat
dc.subject.otherSprague Dawley rat
dc.subject.othertopical treatment
dc.subject.otherWestern blotting
dc.subject.otheranimal
dc.subject.othercomparative study
dc.subject.othercornea disease
dc.subject.othercranial neuropathy
dc.subject.otherdisease model
dc.subject.otherdrug effect
dc.subject.otherdrug therapy
dc.subject.otherinnervation
dc.subject.othermetabolism
dc.subject.otherpathology
dc.subject.othertopical drug administration
dc.titleComparative effects of topical Maresin-1 and cyclosporine A in a capsaicin-induced rat model of neurotrophic keratopathy
dc.typeArticle
rdl.citation.openalex0
rdl.citation.scopus0
rdl.citation.wos0
rdl.departmentDepartment of Ophthalmology, Faculty of Medicine, Fırat University, Elazığ, Turkey
rdl.departmentDepartment of Histology and Embryology, Faculty of Medicine, Fırat University, Elazığ, Turkey
rdl.departmentDepartment of Biochemistry, Faculty of Medicine, Fırat University, Elazığ, Turkey
rdl.departmentDepartment of Veterinary Science, Pertek Sakine Genç Vocational School, Munzur University, Tunceli, Turkey
rdl.oa.statusgreen
rdl.oa.urlhttps://doi.org/10.2139/ssrn.7048513
rdl.scopus.quartileQ1
rdl.sdgSDG03
rdl.source.indexSCOPUS
rdl.source.indexWOS
rdl.source.indexPUBMED
rdl.wos.indexScience Citation Index Expanded (SCI-EXPANDED)