Abdel Mawla M Y, Dingemans K P, Amer M, Venneker G T, van Meegen M, Asghar S S
Department of Dermatology, University of Amsterdam, The Netherlands.
Complement Inflamm. 1991;8(1):50-9. doi: 10.1159/000463177.
A novel polyanionic complement inhibitor 5,5,5''-(1,3,6-naphthalene-triyl-tris[sulfonylimino])-tris(1 ,3-benzene- disulfonic acid) hexasodium salt (compound IIb) was tested for its ability to suppress vascular injury at the site of the Arthus reaction (AR). In control animals in which AR was evoked without drug treatment, venules at AR sites ranged from normal (arbitrarily defined as stage I) to destroyed (stage V). Between these two ends of the spectrum were venules with an accumulation of cells and deposits of electron dense material (stage II), accumulations of cells and deposits and small endothelial gappings (stage III), and accumulations of cells and depositions which had spread into perivascular tissue and small gappings (stage IV). In animals treated with compound IIb, the AR stopped at stage III or IV depending on the dose, it never reached stage V. In other words compound IIb treatment resulted in protection of endothelium, basal lamina and other structures from the destruction which is characteristically observed in the AR. The effect of high doses of compound IIb was similar to that described before for suramin.
一种新型聚阴离子补体抑制剂5,5,5''-(1,3,6-萘三基-三[磺酰亚氨基])-三(1,3-苯二磺酸)六钠盐(化合物IIb),被测试其抑制阿瑟斯反应(AR)部位血管损伤的能力。在未用药物治疗诱发AR的对照动物中,AR部位的小静脉从正常(任意定义为I期)到破坏(Ⅴ期)不等。在这两个极端之间是细胞积聚和电子致密物质沉积的小静脉(Ⅱ期)、细胞积聚、沉积和小的内皮间隙(Ⅲ期),以及细胞积聚和沉积物扩散到血管周围组织和小间隙的情况(Ⅳ期)。在用化合物IIb治疗的动物中,AR根据剂量在Ⅲ期或Ⅳ期停止,从未达到Ⅴ期。换句话说,化合物IIb治疗导致内皮、基膜和其他结构免受AR中典型观察到的破坏。高剂量化合物IIb的效果与之前描述的苏拉明相似。