dc.contributor.author | Eyuboglu, Atilla Adnan | |
dc.contributor.author | Akdemir, Ovunc | |
dc.contributor.author | Erbas, Oytun | |
dc.contributor.author | Isken, Mustafa Tonguc | |
dc.contributor.author | Zhang, Feng | |
dc.contributor.author | Lineaweaver, William C. | |
dc.date.accessioned | 2024-04-29T12:15:17Z | |
dc.date.available | 2024-04-29T12:15:17Z | |
dc.date.issued | 2024 | en_US |
dc.identifier.citation | Eyuboglu, A. A., Akdemir, O., Erbas, O., Isken, M. T., Zhang, F., & Lineaweaver, W. C. (2024). Propionyl-l-carnitine mitigates ischemia-reperfusion injury in rat epigastric island flaps. Heliyon. | en_US |
dc.identifier.issn | 24058440 | |
dc.identifier.uri | https://doi.org/10.1016/j.heliyon.2024.e27448 | |
dc.identifier.uri | https://hdl.handle.net/20.500.12294/4086 | |
dc.description.abstract | Background: Ischemia-reperfusion injury presents a substantial concern in various medical scenarios, notably in reconstructive surgery involving tissue flaps. Despite reports on the protective benefits of Propionyl-L-carnitine against ischemia-reperfusion injury, a thorough assessment of its efficacy in epigastric island flap models is currently lacking. Methods: Sixteen male Sprague-Dawley rats underwent epigastric island flap surgery and were divided into two groups: a Propionyl-L-carnitine group that received intraperitoneal Propionyl-L-carnitine prior to ischemia induction and a sham group that received saline treatment. A comprehensive evaluation was performed including macroscopic, biochemical and histological assessments encompassing measurements of flap survival areas, lipid peroxidation (malondialdehyde), glutathione, myeloperoxidase, nitric oxide and peripheral neutrophil counts. Results: The Propionyl-L-carnitine group demonstrated significantly increased flap survival areas when compared to the sham group. Administration of Propionyl-L-carnitine led to reduced malondialdehyde levels and elevated glutathione levels indicating a reduction in oxidative stress. Furthermore, the Propionyl-L-carnitine group exhibited lower myeloperoxidase levels, higher nitric oxide levels and reduced peripheral neutrophil counts, suggesting a decrease in the inflammatory response. Histopathological analysis revealed decreased levels of inflammation, necrosis, polymorphonuclear leukocyte infiltration and edema in the Propionyl-L-carnitine group. Additionally, vascularity was enhanced in the Propionyl-L-carnitine group. Conclusion: This study provides compelling evidence that Propionyl-L-carnitine administration effectively mitigates the deleterious effects of ischemia-reperfusion injury in epigastric island flaps. This is substantiated by the improved flap survival, diminished oxidative stress and inflammation, as well as the enhanced vascularity observed. Propionyl-L-carnitine emerges as a promising therapeutic intervention to enhance tissue flap survival in reconstructive surgery, warranting further exploration through larger-scale investigations. © 2024 The Authors | en_US |
dc.language.iso | eng | en_US |
dc.publisher | Elsevier Ltd | en_US |
dc.relation.ispartof | HELIYON | en_US |
dc.identifier.doi | 10.1016/j.heliyon.2024.e27448 | en_US |
dc.rights | info:eu-repo/semantics/openAccess | en_US |
dc.subject | NITRIC-OXIDE | en_US |
dc.subject | SURVIVAL | en_US |
dc.subject | ISCHEMIA/REPERFUSION | en_US |
dc.subject | MUSCLE | en_US |
dc.subject | MYELOPEROXIDASE | en_US |
dc.subject | AUGMENTATION | en_US |
dc.title | Propionyl-L-carnitine mitigates ischemia-reperfusion injury in rat epigastric island flaps | en_US |
dc.type | article | en_US |
dc.department | Tıp Fakültesi, Cerrahi Tıp Bilimleri Bölümü | en_US |
dc.authorid | 0000-0002-9805-9830 | en_US |
dc.identifier.volume | 10 | en_US |
dc.identifier.issue | 5 | en_US |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.institutionauthor | Eyuboglu, Atilla Adnan | |
dc.authorwosid | IQW-7940-2023 | en_US |
dc.authorscopusid | 57194466185 | en_US |
dc.identifier.wosquality | Q2 | en_US |
dc.identifier.wos | WOS:001201977000001 | en_US |
dc.identifier.scopus | 2-s2.0-85186989320 | en_US |
dc.identifier.pmid | 38463759 | en_US |