Scopus İndeksli Yayınlar Koleksiyonu
Permanent URI for this collectionhttps://hdl.handle.net/20.500.12514/3596
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Browsing Scopus İndeksli Yayınlar Koleksiyonu by browse.metadata.publisher "Academia Nacional de Medicina"
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Article Liraglutide and Empagliflozin Alleviate Diabetic Cardiomyopathy by Reducing Oxidative Stress and Inflammation(Academia Nacional de Medicina, 2025) Uçar-Ekin, C.; Oflazoğllu-Diken, H.; Baksi, N.; Aşır, F.; Şahika-Gökdemir, G.Background: Diabetes mellitus (DM) is a growing metabolic disease worldwide, associated with severe complications. Glucagon-like peptide-1 analogs and sodium-glucose cotransporter-2 inhibitors are promising therapeutic options for diabetic cardiomyopathy (DCM), although their cardioprotective mechanisms are not yet fully understood. Objective: This study evaluates the effects of liraglutide and empagliflozin on oxidative stress, inflammation, and histological changes in cardiac tissue in DCM. Materials and methods: Thirty-seven male Wistar albino rats were divided into four groups. Diabetes was induced in three groups using streptozotocin and nicotinamide. The groups were: (1) Control, (2) DM, (3) DM + Liraglutide (0.6 mg/kg, subcutaneously, 8 weeks), and (4) DM + Empagliflozin (30 mg/kg, oral gavage, 8 weeks). Blood samples were analyzed through enzyme-linked immunosorbent assay for tumor necrosis factor-α (TNF-α), interleukin-1 (IL-1), malondialdehyde (MDA), superoxide dismutase (SOD), advanced glycation end (AGE) products, and insulin. Cardiac tissue was examined histopathologically. Results: Diabetes significantly increased blood glucose, IL-1, TNF-a, MDA, and AGE (p < 0.01), while SOD levels decreased (p < 0.01), alongside myocardial damage. Liraglutide and empagliflozin improved all parameters (p < 0.01). Conclusion: Liraglutide and empagliflozin mitigate diabetes-induced cardiac damage, likely by reducing fibrosis, oxidative stress, and inflammation. © 2025 Academia Nacional de Medicina de México, A.C. Publicado por Permanyer.
