Molin L, Stendahl O
Acta Med Scand. 1979;206(6):451-7. doi: 10.1111/j.0954-6820.1979.tb13545.x.
Sulfasalazine and its active components, 5-aminosalicylic acid (5-ASA) and sulfapyridine (SP), are potent modulators of inflammatory reactions but with somewhat different modes of action. Investigating the effect of these compounds on normal human polymorphonuclear leukocytes in vitro, we show inhibition of different stages in the phagocytic process, such as migration (sulfasalazine and SP), superoxide production (sulfasalazine and SP), myeloperoxidase-mediated iodination and cytotoxicity (5-ASA and SP). It is thus suggested that sulfasalazine is not just a vehicle for delivering its active components in the colon, but that its therapeutic effect is ulcerative colitis and other inflammatory reactions is a result of the concurrent action of the three compounds.
柳氮磺胺吡啶及其活性成分5-氨基水杨酸(5-ASA)和磺胺吡啶(SP)是炎症反应的有效调节剂,但作用方式略有不同。通过体外研究这些化合物对正常人多形核白细胞的影响,我们发现它们对吞噬过程的不同阶段具有抑制作用,如迁移(柳氮磺胺吡啶和SP)、超氧化物生成(柳氮磺胺吡啶和SP)、髓过氧化物酶介导的碘化反应和细胞毒性(5-ASA和SP)。因此,有人提出柳氮磺胺吡啶不仅仅是在结肠中递送其活性成分的载体,而且其在溃疡性结肠炎和其他炎症反应中的治疗作用是这三种化合物共同作用的结果。