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体外全血中纤维蛋白肽A的裂解与血小板释放。刺激物、抑制剂及搅拌的影响。

Fibrinopeptide A cleavage and platelet release in whole blood in vitro. Effects of stimuli, inhibitors, and agitation.

作者信息

Kaplan K L, Drillings M, Lesznik G

出版信息

J Clin Invest. 1981 May;67(5):1561-8. doi: 10.1172/jci110187.

Abstract

The relationship between platelet release and fibrinopeptide A cleavage from fibrinogen to form fibrin I in vitro was examined in blood allowed to clot undisturbed or with gentle agitation. In undisturbed or agitated blood platelet release and fibrin I formation occurred simultaneously. When hirudin was added to undisturbed blood it prevented platelet release as well as fibrin I formation. In contrast, hirudin added to agitated blood had little effect on platelet release despite complete inhibition of fibrin I formation. Collagen added to either undisturbed or agitated blood increased platelet release and then fibrin I formation, and ADP added to undisturbed blood caused an initial burst of platelet release followed by slight acceleration of fibrinopeptide A cleavage. Prostaglandin E1 and theophylline prevented platelet release in both undisturbed and agitated blood, but did not affect fibrin I formation. The results with inhibitors in agitated blood suggest that fibrin I formation and platelet release can occur independently in the presence of the increased interactions induced by agitation. Addition of thrombin or tissue thromboplastin to undisturbed blood accelerated fibrin I formation with little effect on platelet release. Finally, initial thrombin formation in undisturbed blood appeared to be associated with the platelet surface. These relationships suggest that thrombin formation via the intrinsic system leads to thrombin generation on the platelet surface and simultaneous platelet release and fibrin I formation, while thrombin generated via tissue thromboplastin leads to thrombin formation in the plasma and fibrin I formation preceding platelet release. Activation by interaction of blood with collagen causes initial acceleration of platelet release and later acceleration of fibrin I formation.

摘要

在静置或轻柔搅拌下使其凝固的血液中,研究了体外血小板释放与纤维蛋白原裂解形成纤维蛋白I过程中纤维蛋白肽A裂解之间的关系。在静置或搅拌的血液中,血小板释放和纤维蛋白I形成同时发生。当向静置血液中加入水蛭素时,它会阻止血小板释放以及纤维蛋白I形成。相比之下,向搅拌血液中加入水蛭素对血小板释放影响很小,尽管纤维蛋白I形成被完全抑制。向静置或搅拌血液中加入胶原蛋白会增加血小板释放,随后增加纤维蛋白I形成,向静置血液中加入ADP会导致血小板释放先出现一阵爆发,随后纤维蛋白肽A裂解略有加速。前列腺素E1和茶碱可阻止静置和搅拌血液中的血小板释放,但不影响纤维蛋白I形成。在搅拌血液中使用抑制剂的结果表明,在搅拌引起的相互作用增加的情况下,纤维蛋白I形成和血小板释放可以独立发生。向静置血液中加入凝血酶或组织凝血活酶会加速纤维蛋白I形成,对血小板释放影响很小。最后,静置血液中最初的凝血酶形成似乎与血小板表面有关。这些关系表明,通过内源性系统形成凝血酶会导致血小板表面产生凝血酶,同时发生血小板释放和纤维蛋白I形成,而通过组织凝血活酶产生的凝血酶会导致血浆中凝血酶形成以及在血小板释放之前形成纤维蛋白I。血液与胶原蛋白相互作用激活会导致血小板释放先加速,随后纤维蛋白I形成加速。

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