Ueki H, Tsunemi S, Kubota Y
Gan. 1975 Jun;66(3):237-43.
A hypoalbuminemic substance (F-3), which was obtained from Ehrlich ascites carcinoma cells, showed a marked vascular permeability-increasing action in mice. The highest increasing effect was produced 20 min after an intradermal injection of F-3. This action was inhibited by diisopropyl fluorophosphate, soybean trypsin inhibitor, and indomethacin but not by hydrocortisone or D-2-bromolysergic acid diethylamide. The inhibition of F-3 by diisopropyl fluorophosphate was observed in partial even after the excess diisopropyl fluorophosphate was removed from the diisopropyl fluorophosphate-treated F-3. The hypoalbuminemic and hypoproteinemic actions were not subjected to any inhibition by the diisopropyl fluorophosphate treatment. The decrease in albumin produced 3 hr after the injection of F-3 would be due to the leakage of albumin from blood vessels. F-3 might contain at least two components, one being a vascular permeability-increasing substance and the other a hypoalbuminemic one.
从艾氏腹水癌细胞中获得的一种低白蛋白血症物质(F-3)在小鼠中显示出显著的血管通透性增加作用。皮内注射F-3后20分钟产生的增加效果最为显著。这种作用可被氟磷酸二异丙酯、大豆胰蛋白酶抑制剂和吲哚美辛抑制,但不受氢化可的松或D-2-溴麦角酸二乙酰胺抑制。即使从经氟磷酸二异丙酯处理的F-3中去除过量的氟磷酸二异丙酯后,仍能部分观察到氟磷酸二异丙酯对F-3的抑制作用。氟磷酸二异丙酯处理对低白蛋白血症和低蛋白血症作用没有任何抑制作用。注射F-3后3小时白蛋白的减少可能是由于白蛋白从血管中渗漏所致。F-3可能至少包含两种成分,一种是血管通透性增加物质,另一种是低白蛋白血症物质。