生物优化姜黄作为骨关节炎辅助治疗及其对基因调控(Sirt1)、代谢性炎症和相关症状的影响

S. Bianchi
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引用次数: 0

摘要

背景与目的:骨关节炎(OA)是一种以炎症状态和显著氧化应激为特征的慢性退行性疾病。姜黄因其抗炎和抗氧化活性而闻名,它可以作为标准治疗的替代疗法或与标准治疗一起使用。这种治疗包括止痛剂、类固醇或非甾体抗炎药(NSAIDs),以减轻疼痛和炎症相关症状。本研究旨在探讨生物优化姜黄对骨关节炎患者炎症和相关症状的遗传(SIRT1)和代谢调节的影响。材料与方法:体外实验中,将Hela人细胞接种于12孔板中,与不同浓度的姜黄共孵育3、6、24小时。免疫印迹法评估靶向蛋白表达/磷酸化水平,细胞毒性试验采用CellTiter-Blue细胞活力测定法。在体内研究中,共招募了33例患者,并根据治疗方法分为标准治疗(ST)、ST +姜黄和ST +姜黄+维生素D (2000UI) 3个亚组。健康状况(SF36)和骨关节炎指数(WOMAC评分)在0时进行分析;1、5和3个月时,分别在0和3个月采血,评估炎症标志物、25 (OH) VitD和SIRT1。结果:体外数据显示,活细胞数无统计学意义(p < 0.05)。与对照组相比,各实验组SIRT1的表达和AMP活化蛋白激酶(AMPK)的活化均显著升高(p<0.001)。结果显示,ST +姜黄+ VitD组25(OH) VitD值显著升高(p <0.007),所有姜黄组的SIRT1显著升高(p <0.001)。此外,对于IL-1 (p=0.031)、IL-6 (p=0.031)和IFN-γ (p=0.013),服用姜黄的各组炎症标志物均显著降低,而维生素d没有增加。结论:姜黄作为ST的佐剂,可调节SIRT1通路,显著降低血液炎症标志物,改善骨关节炎的预后。骨关节炎,一种以炎症状态和显著氧化应激为特征的慢性退行性疾病姜黄作为标准治疗的替代或联合治疗生物优化姜黄对炎症的遗传和代谢调节作用SIRT1途径的阳性调节,血液炎症标志物的下降,OA预后更好
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Bio-Optimized Curcuma as Adjuvant Therapy of Osteoarthritis and Its Influence on Gene Regulation (Sirt1), Metabolic Inflammation and Associated Symptoms
Background and aim: Osteoarthritis (OA) is a chronic degenerative disease characterized by an inflammatory state and significant oxidative stress. As curcuma is known for its anti-inflammatory and antioxidant activities, it could be used as alternative therapy next to or together with the standard treatment. This treatment consists of analgesics, steroids or non-steroidal anti-inflammatory drugs (NSAIDs) to reduce pain and inflammation related symptoms. The current study investigates the effect of bio-optimized curcuma on genetic (SIRT1) and metabolic regulation of inflammation and associated symptomatology in patients with osteoarthritis. Materials and methods: In the in vitro study, Hela human cells were seeded in 12-well plates, incubated with curcuma at different concentrations and incubated for 3, 6 and 24 hours. The targeted protein expression/phosphorylation was evaluated by immunoblotting, while cytotoxicity tests were performed by CellTiter-Blue Cell Viability Assay. In the in vivo study, a total of 33 patients were recruited and divided into 3 subgroups based on the treatment: standard treatment (ST), ST + curcuma and ST + curcuma + Vitamin D (2000UI). The health status (SF36) and osteoarthritis index (WOMAC score) were analyzed at 0; 1,5 and 3 months with blood sampling at 0 and 3 months for the evaluation of inflammation markers, 25 (OH) VitD and SIRT1. Results: in vitro data showed no statistically significant decrease (p>0.05) in the number of viable cells. The expression of SIRT1 and the activation of AMP activated protein kinase (AMPK) were significantly increased in all experimental groups compared with the control group (p<0.001). A significant increase in 25(OH) VitD values in the ST + curcuma + VitD group (p <0.007) and in SIRT1 in all groups taking curcuma (p <0.001) was shown. Also for IL-1 (p=0.031), IL-6 (p=0.031) and IFN-γ (p=0.013), all groups taking curcuma showed significantly lower inflammatory markers with no added value of vitamin D. Conclusions: Curcuma as an adjuvant to ST leads to a positive modulation of the SIRT1 pathway, a significant decline of blood inflammatory markers and a better osteoarthritis outcome. Osteoarthritis, a chronic degenerative disease characterized by an inflammatory state and significant oxidative stress Curcuma as alternative therapy next to or together with the standard treatment Effect of bio-optimized curcuma on genetic and metabolic regulation of inflammation Positive modulation of SIRT1 pathway, decline of blood inflammatory markers and a better OA outcome
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