Faculty of Pharmacy, Research Institute of Pharmaceutical Sciences, Musashino University, Tokyo 202-8585, Japan.
Department of Biophysical Chemistry, Kyoto Pharmaceutical University, Kyoto 607-8414, Japan.
Molecules. 2022 Feb 20;27(4):1425. doi: 10.3390/molecules27041425.
Anti-rheumatoid arthritis (RA) effects of α-tocopherol (α-T) have been shown in human patients in a double-blind trial. However, the effects of α-T and its derivatives on fibroblast-like synoviocytes (FLS) during the pathogenesis of RA remain unclear. In the present study, we compared the expression levels of genes related to RA progression in FLS treated with α-T, succinic ester of α-T (TS), and phosphate ester of α-T (TP), as determined via RT-PCR. The mRNA levels of interleukin (IL)-6, tumor necrosis factor-α (TNF-α), matrix metalloproteinase (MMP)-3, and MMP-13 were reduced by treatment with TP without cytotoxicity, while α-T and TS did not show such effects. Furthermore, intraperitoneal injection of TP ameliorated the edema of the foot and joint and improved the arthritis score in laminarin-induced RA model mice. Therefore, TP exerted anti-RA effects through by inhibiting RA-related gene expression.
在一项双盲试验中,已经在人类患者中观察到 α-生育酚(α-T)的抗风湿性关节炎(RA)作用。然而,α-T 及其衍生物在 RA 发病机制中对成纤维样滑膜细胞(FLS)的影响尚不清楚。在本研究中,我们通过 RT-PCR 比较了用 α-T、α-T 的琥珀酸酯(TS)和磷酸酯(TP)处理的 FLS 中与 RA 进展相关的基因的表达水平。TP 处理没有细胞毒性,但可降低白细胞介素(IL)-6、肿瘤坏死因子-α(TNF-α)、基质金属蛋白酶(MMP)-3 和 MMP-13 的 mRNA 水平,而 α-T 和 TS 则没有这种作用。此外,TP 的腹腔内注射可改善角叉菜胶诱导的 RA 模型小鼠的足部和关节水肿,并改善关节炎评分。因此,TP 通过抑制 RA 相关基因的表达发挥抗 RA 作用。