Department of Orthopedics, Tianshui First People's Hospital, Tianshui City, Gansu Province, China.
Department of Anesthesiology, Tianshui First People's Hospital, Tianshui City, Gansu Province, China.
J Physiol Pharmacol. 2023 Dec;74(6). doi: 10.26402/jpp.2023.6.08. Epub 2024 Feb 7.
Withaferin A (WFA) is a natural compound separated from the medicinal plant Withania somnifera. As reported, it has the potential to safely cure rheumatoid arthritis (RA) in animal models. Nevertheless, the action mechanism of WFA in treating RA has not been completely illuminated. The study was to explore the action and mechanism of WFA on arthritic rats. First, a collagen-induced arthritis rat model was established. WFA administration alleviated inflammation and injury in arthritic rats. Subsequently, fibroblast synovial cells (FLS) of arthritic rats were separated and cell proliferation and apoptosis abilities were tested. It was found that WFA was available to repress FLS cell proliferation and accelerate apoptosis. MicroRNA-1297 was downregulated in RA patients. Clinical correlation analysis suggested that miR-1297 in the serum of RA patients was negatively associated with pro-inflammatory factors interleukin (IL)-6, IL-17, tumor necrosis factor (TNF)-α, and RA diagnostic indexes (RF, DAS28). In the meantime, miR-1297 had superior diagnostic value in differentiating RA patients from healthy people. Karyopherin α2 (KPNA2) was the downstream target of miR-1297, while miR-1297 negatively modulated KPNA2 expression. Importantly, WFA further restrained KPNA2 expression via elevating miR-1297 in functional rescue experiments, thereby treating inflammation and injury in arthritic rats and repressing FLS cell proliferation and activation. In short, WFA alleviated inflammation and joint damage in arthritic rats via elevating miR-1297 to target KPNA2.
Withaferin A (WFA) 是一种从药用植物印度萝芙木中分离出来的天然化合物。据报道,它有潜力在动物模型中安全地治愈类风湿关节炎(RA)。然而,WFA 治疗 RA 的作用机制尚未完全阐明。本研究旨在探讨 WFA 对关节炎大鼠的作用和机制。首先,建立了胶原诱导性关节炎大鼠模型。WFA 给药缓解了关节炎大鼠的炎症和损伤。随后,分离关节炎大鼠的成纤维样滑膜细胞(FLS),并测试其增殖和凋亡能力。结果发现,WFA 能够抑制 FLS 细胞增殖并加速其凋亡。在 RA 患者中,miR-1297 下调。临床相关性分析表明,RA 患者血清中 miR-1297 与促炎因子白细胞介素(IL)-6、IL-17、肿瘤坏死因子(TNF)-α 和 RA 诊断指标(RF、DAS28)呈负相关。同时,miR-1297 在区分 RA 患者与健康人群方面具有较高的诊断价值。核孔蛋白 α2(KPNA2)是 miR-1297 的下游靶标,而 miR-1297 负调控 KPNA2 的表达。重要的是,在功能挽救实验中,WFA 通过升高 miR-1297 进一步抑制 KPNA2 的表达,从而治疗关节炎大鼠的炎症和损伤,并抑制 FLS 细胞的增殖和活化。总之,WFA 通过升高 miR-1297 靶向 KPNA2 减轻关节炎大鼠的炎症和关节损伤。