Nesher G, Moore T L, Dorner R W
Department of Internal Medicine, St Louis University School of Medicine, MO 63104.
Ann Rheum Dis. 1991 Sep;50(9):637-41. doi: 10.1136/ard.50.9.637.
The mechanism of action of low dose methotrexate in rheumatoid arthritis has not been established. It has been shown to have an anti-inflammatory effect and to inhibit neutrophil chemotaxis, but the effect on monocytes has not been widely studied. Normal donor peripheral blood monocytes were incubated with methotrexate in vitro and their superoxide production, chemotaxis, and phagocytosis subsequently assessed. Additionally, the influence of different culture media, and of folinic acid, and the methyl donor S-adenosylmethionine, and spermidine on the methotrexate mediated effects were evaluated. It was found that methotrexate in low concentrations inhibited in vitro monocyte chemotaxis and superoxide production but only after prolonged incubation. This inhibition was augmented by incubation in medium containing a low methionine concentration and was abolished by folinic acid and S-adenosylmethionine, suggesting that methotrexate may interfere with specific methylation reactions.
低剂量甲氨蝶呤在类风湿性关节炎中的作用机制尚未明确。已证实其具有抗炎作用并能抑制中性粒细胞趋化性,但对单核细胞的作用尚未得到广泛研究。将正常供体的外周血单核细胞与甲氨蝶呤在体外进行孵育,随后评估其超氧化物生成、趋化性和吞噬作用。此外,还评估了不同培养基、亚叶酸、甲基供体S-腺苷甲硫氨酸和亚精胺对甲氨蝶呤介导作用的影响。研究发现,低浓度的甲氨蝶呤仅在长时间孵育后才会抑制体外单核细胞趋化性和超氧化物生成。在含低蛋氨酸浓度的培养基中孵育可增强这种抑制作用,而亚叶酸和S-腺苷甲硫氨酸可消除这种抑制作用,这表明甲氨蝶呤可能会干扰特定的甲基化反应。