Jaques L B, Hiebert L M, Wice S M
Department of Oral Biology, College of Dentistry, University of Saskatchewan, Saskatoon, Canada.
J Lab Clin Med. 1991 Feb;117(2):122-30.
Heparin, hydrogenated dextran sulfate 8000 (Usherdex 8), and dextran sulfate 8000 were administered to rats, and the total drug was separated and determined in endothelium and plasma. A large amount of each drug was recovered from endothelium 2.4 and 6 minutes after intravenous injection. This accounted for the drug missing from plasma. The drugs in water were placed in the stomach by catheter. All three drugs were recovered from the endothelium and identified unchanged by electrophoresis and specific staining. The amounts that were recovered at 2.4 and 6 minutes were equivalent to most of the drug administered. Thus heparin, Usherdex 8, and dextran sulfate 8000 enter the body immediately on oral administration. At longer time intervals after intravenous and oral administration, much of each drug was not demonstrable in endothelium by the method used. Some drug could be detected in endothelium after 4 hours. After oral administration, plasma levels of each drug were rarely more than 0.5% of the dose. Formalin-alcohol was applied to the jugular veins of anesthetized rats to produce a thrombus, (see Blake et al. J Clin Path 1959;12:118-22) and the drugs were immediately introduced into the stomach. Four hours later the injured veins were inspected for thrombi. Incidence of thrombotic plug was 80% in rats that received saline solution, 4% with Usherdex 8, 0% with dextran sulfate 8000, and 0% with heparin. Usherdex 8, dextran sulfate 8000, and heparin demonstrate low, moderate, and high in vitro anticoagulant activity, respectively.(ABSTRACT TRUNCATED AT 250 WORDS)
将肝素、氢化硫酸葡聚糖8000(优素得8)和硫酸葡聚糖8000给予大鼠,然后分离并测定内皮和血浆中的总药物量。静脉注射后2.4分钟和6分钟,从内皮中回收了大量每种药物。这解释了血浆中药物的缺失情况。将水中的药物通过导管置于胃中。通过电泳和特异性染色,从内皮中回收了所有三种药物,并鉴定其未发生变化。在2.4分钟和6分钟回收的量相当于所给药的大部分药物。因此,肝素、优素得8和硫酸葡聚糖8000口服后立即进入体内。在静脉注射和口服后的较长时间间隔,用所用方法在内皮中无法检测到大部分每种药物。4小时后可在内皮中检测到一些药物。口服给药后,每种药物的血浆水平很少超过剂量的0.5%。对麻醉大鼠的颈静脉应用福尔马林-酒精以形成血栓(见布莱克等人,《临床病理学杂志》1959年;12:118 - 22),并立即将药物引入胃中。4小时后检查受伤静脉中的血栓。接受生理盐水的大鼠血栓形成栓子的发生率为80%,接受优素得8的为4%,接受硫酸葡聚糖8000的为0%,接受肝素的为0%。优素得8、硫酸葡聚糖8000和肝素分别表现出低、中、高的体外抗凝活性。(摘要截取自250字)