Lee Yun-Mi, Kim Dong-Seon
KM Science Research Division, Korea Institute of Oriental Medicine, Daejeon 34054, Republic of Korea.
Int J Mol Sci. 2024 Apr 12;25(8):4268. doi: 10.3390/ijms25084268.
Inflammation is crucial to osteoarthritis (OA) pathogenesis. The aim of this study was to evaluate residue extract (NHGRE) obtained by extracting fruits with water as a potential food supplement for treating arthritis based on its analgesic, anti-inflammatory, and chondroprotective effects and the remaining residue with 70% ethanol. We observed the analgesic activity of NHGRE based on the acetic acid-induced writhing response in mice, examined its anti-inflammatory efficacy against carrageenan-induced paw oedema in mice, and investigated its effect on inflammatory cytokine expression in interleukin (IL)-1β-induced SW1353 cells. Furthermore, we determined its effects on cartilage protection in interleukin-1β (IL-1β)-treated SW1353 cells. NHGRE at 200 mg/kg significantly reduced the acetic acid-induced writhing response and prevented oedema formation in the carrageenan-induced paw oedema model. In IL-1β-induced SW1353 cells, NHGRE at 400 µg/mL reduced the expression of inflammation mediators such as tumour necrosis factor (TNF)-α (55.3%), IL-6 (35.4%), and prostaglandin E2 (PGE2) (36.9%) and down-regulated the expression of matrix metalloproteinase (MMP)-1 (38.6%), MMP-3 (29.3%), and MMP-13 (44.8%). Additionally, it restored degraded collagen II levels in chondrocytes. NHGRE plays a protective role in chondrocytes by regulating Nuclear factor kappa B (NF-κB) activation. Overall, NHGRE may be a useful therapeutic agent for OA by controlling pain, oedema formation, and inflammation-related mechanisms.
炎症对于骨关节炎(OA)的发病机制至关重要。本研究的目的是评估用水提取水果获得的残渣提取物(NHGRE)作为一种潜在的食品补充剂,基于其镇痛、抗炎和软骨保护作用以及用70%乙醇提取后的剩余残渣来治疗关节炎。我们基于乙酸诱导的小鼠扭体反应观察了NHGRE的镇痛活性,检测了其对角叉菜胶诱导的小鼠足爪肿胀的抗炎功效,并研究了其对白细胞介素(IL)-1β诱导的SW1353细胞中炎性细胞因子表达的影响。此外,我们确定了其对白细胞介素-1β(IL-1β)处理的SW1353细胞中软骨保护的作用。200mg/kg的NHGRE显著降低了乙酸诱导的扭体反应,并在角叉菜胶诱导的足爪肿胀模型中预防了水肿形成。在IL-1β诱导的SW1353细胞中,400μg/mL的NHGRE降低了炎症介质如肿瘤坏死因子(TNF)-α(55.3%)、IL-6(35.4%)和前列腺素E2(PGE2)(36.9%)的表达,并下调了基质金属蛋白酶(MMP)-1(38.6%)、MMP-3(29.3%)和MMP-13(44.8%)的表达。此外,它恢复了软骨细胞中降解的胶原蛋白II水平。NHGRE通过调节核因子κB(NF-κB)激活在软骨细胞中发挥保护作用。总体而言,NHGRE可能是一种通过控制疼痛、水肿形成和炎症相关机制来治疗OA的有用治疗剂。