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蛇毒成分对血小板功能的影响。

Snake Venom Constituents that Affect Platelet Function.

机构信息

Pharmacological Institute, College of Medicine, National Taiwan University, Taipei, Taiwan.

出版信息

Platelets. 1991;2(2):77-87. doi: 10.3109/09537109109113692.

Abstract

Snake venoms contain complex mixtures of proteins with biological activities. These venom proteins affect blood coagulation and platelet function in various ways. Many inducers and inhibitors of platelet aggregation have been isolated from snake venoms, especially from the Crotalidae and Viperidae families. According to their biochemical properties and modes of action, they can be classified into ten groups: (1) thrombin-like enzymes which show higher activity towards platelets than towards fibrinogen; (2) procoagulant enzymes which generate thrombin and then activate platelets indirectly; (3) noncoagulant glycoproteins which activate platelets independently of ADP release or thromboxane formation; (4) lectin-like peptides which cause agglutination of platelets through binding to a sugar moiety; (5) coagglutinins whose activities are dependent on the presence of von Willebrand factor (vWF); (6) membrane-active polypeptides which potentiate the aggregating action of other inducers by activation of platelet endogenous phospholipase A(2); (7) phospholipase A(2) enzymes which show biphasic aggregating and inhibitory effects on platelets; (8) α-fibrinogenases which degrade the α (A) chain of fibrinogen; (9) 5'-nucleotidase or ADPase which act on the ADP released from platelet dense bodies; and (10) fibrinogen-receptor antagonists which interfere with the interaction of fibrinogen and glycoprotein IIb/IIIa on activated platelets. These venom proteins are unique research tools for study of the haemostatic process and some of them are potential antithrombotic agents.

摘要

蛇毒含有复杂的蛋白质混合物,具有生物活性。这些毒液蛋白以各种方式影响血液凝固和血小板功能。许多血小板聚集的诱导剂和抑制剂已从蛇毒中分离出来,特别是从响尾蛇科和蝰蛇科中分离出来。根据它们的生化性质和作用方式,它们可以分为十组:(1)类凝血酶酶,对血小板的活性比对纤维蛋白原的活性更高;(2)促凝血酶酶,产生凝血酶,然后间接激活血小板;(3)非凝血糖蛋白,独立于 ADP 释放或血栓烷形成激活血小板;(4)凝集素样肽,通过与糖部分结合引起血小板凝集;(5)依赖 von Willebrand 因子(vWF)的凝血素,其活性依赖于 vWF 的存在;(6)膜活性多肽,通过激活血小板内源性磷脂酶 A(2)增强其他诱导剂的聚集作用;(7)磷脂酶 A(2)酶,对血小板具有双相聚集和抑制作用;(8)α-纤维蛋白溶酶,降解纤维蛋白原的α(A)链;(9)5'-核苷酸酶或 ADP 酶,作用于从血小板致密体释放的 ADP;(10)纤维蛋白原受体拮抗剂,干扰纤维蛋白原与激活血小板上的糖蛋白 IIb/IIIa 的相互作用。这些毒液蛋白是研究止血过程的独特研究工具,其中一些是潜在的抗血栓形成剂。

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