Zuanazzi Pasinato Aline, Vargas José Eduardo, Spanhol da Silva Julia, Grandó Moretto Joana, Ferreira Teixeira Cibele, Farina Azzolin Verônica, Mânica da Cruz Ivana Beatrice, da Rosa Trevisan Camile, Zub Emanuele Cristina, Puga Renato, Vargas Verónica Inés, León-Mejía Grethel, Pillon Barcelos Rômulo
Institute of Biological Sciences, University of Passo Fundo (UPF), Passo Fundo 99042-800, Rio Grande do Sul, Brazil.
Laboratory of Inflammatory and Neoplastic Cells, Department of Cell Biology, Federal University of Paraná (UFPR), Curitiba 80060-000, Paraná, Brazil.
Antioxidants (Basel). 2025 Jul 18;14(7):881. doi: 10.3390/antiox14070881.
Osteoarthritis (OA) is a progressive joint disease that is commonly managed with palliative drugs, many of which are associated with undesirable side effects. This study investigated the therapeutic potential of a novel supplementation with guarana, selenium, and L-carnitine (GSC) in a rat model of chemically induced OA. Forty male Wistar rats (8-9 weeks old) received intra-articular sodium monoiodoacetate (Mia) to induce OA, and were subsequently treated with GSC. Inflammatory and oxidative stress parameters were analyzed at the end of the experiment. GSC supplementation enhanced endogenous antioxidant defenses, suggesting systemic antioxidant activity. However, no histological improvement was observed. In silico analyses indicated that Mia-induced OA may involve a complex molecular environment that GSC, at the tested dose, failed to modulate at the site of injury. Despite the limited local effects, these findings support the systemic benefits of GSC and highlight the potential of natural compound-based strategies in OA management. Given the adverse effects of conventional pharmacotherapy, the development of alternative, naturally derived treatments remains a promising avenue for future research.
骨关节炎(OA)是一种进行性关节疾病,通常使用姑息性药物进行治疗,其中许多药物都伴有不良副作用。本研究在化学诱导的OA大鼠模型中研究了一种新型的瓜拉那、硒和左旋肉碱(GSC)补充剂的治疗潜力。40只雄性Wistar大鼠(8 - 9周龄)接受关节内注射单碘乙酸钠(MIA)以诱导OA,随后用GSC进行治疗。在实验结束时分析炎症和氧化应激参数。补充GSC增强了内源性抗氧化防御,表明具有全身抗氧化活性。然而,未观察到组织学改善。计算机模拟分析表明,MIA诱导的OA可能涉及一个复杂的分子环境,在所测试的剂量下,GSC未能在损伤部位进行调节。尽管局部作用有限,但这些发现支持了GSC的全身益处,并突出了基于天然化合物的策略在OA管理中的潜力。鉴于传统药物治疗的不良反应,开发替代性的天然衍生治疗方法仍然是未来研究的一个有前景的途径。