Fan Kai-Jian, Wu Jing, Wang Qi-Shan, Xu Bing-Xin, Zhao Fu-Tao, Wang Ting-Yu
Department of Pharmacy, Shanghai Ninth People's Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai, China.
Department of Rheumatology, Shanghai Ninth People's Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai, China.
Ann Transl Med. 2020 Dec;8(23):1565. doi: 10.21037/atm-20-3042.
Metformin (MF) is a widely used biguanide oral hypoglycemic agent, which has obvious anti-inflammatory and immunomodulatory effects. However, the mechanism of MF on rheumatoid arthritis (RA) remains uncertain. In this study, we investigated the therapeutic effects of MF on collagen-induced arthritis (CIA).
CIA was induced in rats by intradermal injection of a mixture of bovine type II collagen and incomplete Freund's adjuvant (IFA) on day 0 and day 7 through the base of the tail. Intraperitoneal injection of MF (100 mg/kg) was given every 3 days, from day 14 for 3 weeks. The effects of MF on arthritis-induced systemic inflammation and synovitis were studied by pathological analysis of the knee joint and serological examination of peripheral blood in CIA rats. The bone protection effect of MF was studied by microscopic computed tomography (micro-CT) and histological analysis of the knee joint. The effects of MF on chondrocytes in CIA rats were studied by detecting the relevant pro-apoptotic mediators in the chondrocytes.
After administration of MF in CIA rats, systemic inflammation and synovitis caused by arthritis were significantly suppressed. Histomorphometry and micro-CT analysis of the knee joint revealed that MF can protect bone by inhibiting the changes of trabecular bone in CIA rats. Histological analysis of the knee joint found that MF can inhibit osteoclast formation and degradation of the cartilage layer matrix. Detection of the relevant pro-apoptotic mediators in chondrocytes revealed that MF can significantly inhibit the apoptosis of chondrocytes in CIA rats.
Our study showed that MF can inhibit systemic inflammation and synovitis and plays a role in bone protection by inhibiting cartilage layer matrix degradation, osteoclast formation, and chondrocyte apoptosis.
二甲双胍(MF)是一种广泛使用的双胍类口服降糖药,具有明显的抗炎和免疫调节作用。然而,MF对类风湿关节炎(RA)的作用机制仍不明确。在本研究中,我们调查了MF对胶原诱导性关节炎(CIA)的治疗效果。
于第0天和第7天通过大鼠尾根部皮内注射牛II型胶原和不完全弗氏佐剂(IFA)混合物诱导大鼠发生CIA。从第14天开始,每3天腹腔注射MF(100 mg/kg),持续3周。通过对CIA大鼠膝关节进行病理分析和外周血血清学检查,研究MF对关节炎引起的全身炎症和滑膜炎的影响。通过显微计算机断层扫描(micro-CT)和膝关节组织学分析,研究MF的骨保护作用。通过检测软骨细胞中相关促凋亡介质,研究MF对CIA大鼠软骨细胞的影响。
在CIA大鼠中给予MF后,关节炎引起的全身炎症和滑膜炎得到显著抑制。膝关节组织形态计量学和micro-CT分析显示,MF可通过抑制CIA大鼠小梁骨的变化来保护骨骼。膝关节组织学分析发现,MF可抑制破骨细胞形成和软骨层基质降解。软骨细胞中相关促凋亡介质的检测显示,MF可显著抑制CIA大鼠软骨细胞的凋亡。
我们的研究表明,MF可抑制全身炎症和滑膜炎,并通过抑制软骨层基质降解、破骨细胞形成和软骨细胞凋亡发挥骨保护作用。