Parry E W
Department of Human Anatomy and Cell Biology, University of Liverpool, U.K.
J Comp Pathol. 1991 Feb;104(2):121-7. doi: 10.1016/s0021-9975(08)80095-3.
The glomerular capillary coagulation in mice which follows challenge with cycloheximide and a submicrogram dose of endotoxin was shown to become fully established between 4 h and 6 h after challenge. Complete protection against the renal lesion was achieved by heparin treatment 4 h after challenge. The antifibrinolytic agent, tranexamic acid, given 4 h and 6 h after challenge, abolished this heparin-induced protection, but had no effect when given 6 h and 8 h after challenge. These findings suggest that heparin in some way delayed the onset of cycloheximide and endotoxin-induced irreversible coagulation in glomerular capillaries, and by so doing, allowed the development of local, protective, fibrinolytic activity. A relatively brief period of such fibrinolytic activity appeared to confer lasting protection against coagulation in glomerular capillaries. Appropriately timed treatment with hydrocortisone also abolished the heparin-initiated protection, and the evidence suggests that the steroid acts by inhibiting the development of local fibrinolytic activity.
在用环己酰亚胺和亚微克剂量的内毒素攻击后,小鼠肾小球毛细血管内的凝血在攻击后4小时至6小时之间完全形成。在攻击后4小时用肝素治疗可完全预防肾脏损伤。在攻击后4小时和6小时给予抗纤维蛋白溶解剂氨甲环酸,可消除肝素诱导的这种保护作用,但在攻击后6小时和8小时给予则无效。这些发现表明,肝素以某种方式延迟了环己酰亚胺和内毒素诱导的肾小球毛细血管不可逆凝血的发生,并通过这样做,使局部保护性纤维蛋白溶解活性得以发展。相对短暂的这种纤维蛋白溶解活性似乎赋予了对肾小球毛细血管内凝血的持久保护。用氢化可的松进行适当时间的治疗也消除了肝素引发的保护作用,证据表明类固醇的作用是抑制局部纤维蛋白溶解活性的发展。