Howard M A, Perkin J, Salem H H, Firkin B G
Br J Haematol. 1984 May;57(1):25-35. doi: 10.1111/j.1365-2141.1984.tb02862.x.
Botrocetin caused a factor VIII (FVIII) dependent platelet agglutination which was associated with a reduction in the plasma levels of all FVIII parameters as a result of specific binding of FVIII to the platelets. The site of binding of FVIII to the platelet in response to ristocetin or botrocetin involves the glycoprotein I complex. This is suggested by the inability of chymotrypsin treated platelets or platelets from patients with the Bernard-Soulier syndrome to agglutinate in response to ristocetin. These platelets responded to botrocetin , but this was greatly reduced compared to normal. Crossed immunoelectrophoretic analysis indicated that in the presence of botrocetin most multimetric forms of FVIII bound to the platelet, whereas ristocetin caused binding of high and intermediate molecular weight forms. The antibiotic vancomycin inhibited platelet agglutination by ristocetin but had no effect on that caused by botrocetin . Assays of FVIII von Willebrand factor (VIII:vWf) using botrocetin compared well with those obtained using ristocetin in plasmas from normal individuals and from patients with classical von Willebrand disease (vWd). However, a patient with variant vWd demonstrated 100% botrocetin cofactor activity and 0% ristocetin cofactor activity. This suggested that the site of interaction on the FVIII molecule for botrocetin and ristocetin are different. Therefore the diagnosis of some von Willebrand variants cannot be excluded on the basis of a normal botrocetin cofactor assay.
蛇毒巴曲酶可引起依赖因子VIII(FVIII)的血小板凝集,这与所有FVIII参数的血浆水平降低有关,因为FVIII与血小板特异性结合。FVIII对瑞斯托霉素或蛇毒巴曲酶反应时与血小板的结合位点涉及糖蛋白I复合物。这是由经胰凝乳蛋白酶处理的血小板或患有伯纳德-索利尔综合征患者的血小板对瑞斯托霉素无凝集反应所提示的。这些血小板对蛇毒巴曲酶有反应,但与正常情况相比大大降低。交叉免疫电泳分析表明,在蛇毒巴曲酶存在的情况下,大多数多聚体形式的FVIII与血小板结合,而瑞斯托霉素导致高分子量和中等分子量形式的结合。抗生素万古霉素可抑制瑞斯托霉素引起的血小板凝集,但对蛇毒巴曲酶引起的凝集无影响。在正常个体和典型血管性血友病(vWd)患者的血浆中,使用蛇毒巴曲酶检测FVIII血管性血友病因子(VIII:vWf)与使用瑞斯托霉素检测的结果相当。然而,一名变异型vWd患者显示蛇毒巴曲酶辅因子活性为100%,瑞斯托霉素辅因子活性为0%。这表明蛇毒巴曲酶和瑞斯托霉素在FVIII分子上的相互作用位点不同。因此,不能基于蛇毒巴曲酶辅因子检测正常而排除某些血管性血友病变异型的诊断。