Kumada T, Abiko Y
Thromb Haemost. 1976 Nov 30;36(2):451-64.
The effect of long-term ingestion of an anabolic steroid, furazabol, was studied on coagulo-fibrinolytic systems in the rat. During the administration of furazabol at the daily dose of 0.04, 0.2 or 1 mg/rat for 3 months, the most remarkable changes were increase in the plasminogen activator activity in blood and the lung tissue and decrease in plasma fibrinogen level as well as decrease in plasma cholesterol. It was a very important finding that in most of the rats the furazabol treatment was effective in reducing susceptibility to lactic acidosis-induced pulmonary thrombosis. No meaningful changes were observed in other parameters tested including ADP-induced platelet aggregability, plasma recalcification time, plasma plasminogen, plasma antiplasmin activity, plasminogen activator content of tissues other than the lungs and the release of vascular activator induced by venous occlusion. One month after cessation of the furazabol treatment, these altered parameters tended to return to normal. Independently on the furazabol treatment, highly significant positive correlation existed between the plasma activator activity and the pulmonary tissue activator content. This indicated that the major source of plasma activator in the rat was the lung tissue and that the furazabol treatment increased the circulating activator activity through enhancing activator content in the lungs.
研究了长期摄入合成代谢类固醇呋咱甲氢龙对大鼠凝血-纤溶系统的影响。在以0.04、0.2或1mg/大鼠的日剂量给予呋咱甲氢龙3个月的过程中,最显著的变化是血液和肺组织中纤溶酶原激活物活性增加,血浆纤维蛋白原水平降低以及血浆胆固醇降低。一个非常重要的发现是,在大多数大鼠中,呋咱甲氢龙治疗可有效降低对乳酸酸中毒诱导的肺血栓形成的易感性。在测试的其他参数中未观察到有意义的变化,包括ADP诱导的血小板聚集性、血浆复钙时间、血浆纤溶酶原、血浆抗纤溶酶活性、肺以外组织的纤溶酶原激活物含量以及静脉闭塞诱导的血管激活物释放。停止呋咱甲氢龙治疗1个月后,这些改变的参数趋于恢复正常。与呋咱甲氢龙治疗无关,血浆激活物活性与肺组织激活物含量之间存在高度显著的正相关。这表明大鼠血浆激活物的主要来源是肺组织,并且呋咱甲氢龙治疗通过提高肺中的激活物含量来增加循环激活物活性。