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dc.contributor.authorOk, Muhammet Uğur
dc.contributor.authorŞahin, Rıfat
dc.contributor.authorBalık, Mehmet Sabri
dc.contributor.authorOkcu, Oğuzhan
dc.date.accessioned2023-10-27T11:28:39Z
dc.date.available2023-10-27T11:28:39Z
dc.date.issued2023en_US
dc.identifier.citationOk, M. U., Şahin, R., Balik, M. S., & Okçu, O. (2023). The healing effects of L-carnitine and spongostan on cartilage defect in rat model. Injury, 111115. Advance online publication. https://doi.org/10.1016/j.injury.2023.111115en_US
dc.identifier.issn0020-1383
dc.identifier.issn1879-0267
dc.identifier.issn0020-1383
dc.identifier.urihttps://doi.org/10.1016/j.injury.2023.111115
dc.identifier.urihttps://hdl.handle.net/11436/8589
dc.description.abstractPurpose: We aimed to determine the effect of L-carnitine and spongostan on cartilage healing in an experimental animal model with a full-thickness cartilage defect. Methods: In the study 32 Sprague–Dawley rats were divided into four groups in equal numbers. A cartilage defect with a diameter of 1 mm and a depth of 3 mm was created in the femoral intercondylar region of rats in groups A, B, and C. Group A received no treatment in the defective area. Group B received treatment with spongostan. Group C received treatment with spongostan soaked in L-carnitine. Group D served as the healthy control group. The rats were euthanized 6 weeks after the treatment. Histological evaluation of the condyles was done with the modified Mankin scoring. Results: In the histopathological imaging of the cartilage structure, it was observed that in group A, there was complete disorganization and cellular structure was completely absent up to the subchondral bone. In group B, moderate structural improvement, partially intact appearance in border integrity and mostly diffuse hypercellularity were observed. In group C, a near-normal healing, a completely intact appearance in boundary integrities and normal or hypercellularity in cellular structure were observed. The total score of the modified Mankin decreases numerically from A to D. There was no statistically significant difference observed between the A-B (p = 0.176), C-D (p = 0.145), and C-B (p = 0.580) groups, while significant differences were detected between the A–C (p = 0.004), B–D (p = 0.007), and A–D (p = 0.000) groups. Conclusion: It has been known that mitochondrial activity is reduced in the osteoarthritis, and as a result, decrease in cellular activity occurs with ATP synthesis. For this reason, we found that L-carnitine, which we expect to stimulate cell proliferation by stimulating ATP synthesis, makes a positive contribution to cartilage healing, as expected. It has been found that combining spongostan with L-carnitine for the treatment of cartilage healing, instead of applying spongostan alone, provides near-normal healing.en_US
dc.language.isoengen_US
dc.publisherElsevieren_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectCartilageen_US
dc.subjectSpongostanen_US
dc.subjectL-carnitineen_US
dc.subjectMankin scoreen_US
dc.subjectOsteochondral lesionen_US
dc.titleThe healing effects of L-carnitine and spongostan on cartilage defect in rat modelen_US
dc.typearticleen_US
dc.contributor.departmentRTEÜ, Tıp Fakültesi, Cerrahi Tıp Bilimleri Bölümüen_US
dc.contributor.institutionauthorŞahin, Rıfat
dc.contributor.institutionauthorBalık, Mehmet Sabri
dc.contributor.institutionauthorOkcu, Oğuzhan
dc.identifier.doi10.1016/j.injury.2023.111115en_US
dc.relation.journalInjuryen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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