Janusz M J, Hare M
Marion Merrell Dow Research Institute, Cincinnati, OH 45215.
Int J Immunopharmacol. 1994 Aug;16(8):623-32. doi: 10.1016/0192-0561(94)90135-x.
The sulfated polymer MDL 101,028 was found to be a potent-inhibitor of both human neutrophil elastase (HNE) and human neutrophil cathepsin G (CatG). Cleavage of synthetic substrate by HNE was inhibited by MDL 101,028 with an IC50 of 40 nM, while CatG was inhibited with an IC50 of 80 nM. Degradation of a macromolecular connective tissue substrate (cartilage proteoglycan) by HNE or CatG was inhibited by MDL 101,028 with an IC50 of approximately 10 microM. MDL 101,028 at concentrations of 4, 10 and 25 microM inhibited degradation of cartilage proteoglycan by human neutrophil lysate or stimulated human neutrophils by 54%, 70% and 79%, and 31%, 47% and 73%, respectively. Acute pulmonary injury resulting from the intratracheal (i.t.) instillation of HNE in rats was inhibited by 48%, 90% and 90% at concentrations of MDL 101,028 of 1.1 mg/kg, 2.8 mg/kg and 11 mg/kg. The duration of action of the compound after i.t. instillation was between 2 and 4 h. These results suggest that sulfated polymers such as MDL 101,146 may be useful as inhibitors of HNE-mediated lung injury.
硫酸化聚合物MDL 101,028被发现是人类中性粒细胞弹性蛋白酶(HNE)和人类中性粒细胞组织蛋白酶G(CatG)的有效抑制剂。MDL 101,028抑制HNE对合成底物的切割,其半数抑制浓度(IC50)为40 nM,而对CatG的抑制IC50为80 nM。MDL 101,028抑制HNE或CatG对大分子结缔组织底物(软骨蛋白聚糖)的降解,IC50约为10 μM。浓度为4、10和25 μM的MDL 101,028分别抑制人类中性粒细胞裂解液对软骨蛋白聚糖的降解或抑制受刺激的人类中性粒细胞,抑制率分别为54%、70%和79%,以及31%、47%和73%。大鼠气管内(i.t.)注入HNE导致的急性肺损伤,在MDL 101,028浓度为1.1 mg/kg、2.8 mg/kg和11 mg/kg时,抑制率分别为48%、90%和90%。i.t.注入该化合物后的作用持续时间为2至4小时。这些结果表明,诸如MDL 101,146之类的硫酸化聚合物可能作为HNE介导的肺损伤的抑制剂有用。