Effects of Native Fucosylated Glycosaminoglycan, Its Depolymerized Derivatives on Intrinsic Factor Xase, Coagulation, Thrombosis, and Hemorrhagic Risk

Thromb Haemost. 2020 Apr;120(4):607-619. doi: 10.1055/s-0040-1708480. Epub 2020 Apr 14.

Abstract

A native fucosylated glycosaminoglycan from sea cucumber Holothuria fuscopunctata (nHG), mainly branched with Fuc3S4S, exhibited potent anticoagulant activity by intrinsic tenase iXase (FIXa-FVIIIa complex) and antithrombin-dependent factor IIa (FIIa) inhibition, but also had the effects of FXII activation and platelet aggregation. For screening a selective iXase inhibitor, depolymerized nHG (dHG-1 ∼ -6) and a pure octasaccharide (oHG-8) were prepared. Like nHG, dHG-1 ∼ -6 and oHG-8 could potently inhibit iXase, and competitive binding assay indicated that dHG-5 and oHG-8 could bind to FIXa. Nevertheless, dHG-5 and oHG-8 had no effects on FXII and platelet activation. nHG, dHG-5, and oHG-8 could significantly prolong the activated partial thromboplastin time of human, rat, and rabbit plasma. In the rat deep venous thrombosis model, dHG-5 and oHG-8 showed potent antithrombotic effects in a dose-dependent manner, while the thrombus inhibition rate of nHG at high dose was markedly reduced. Additionally, dHG-5 and oHG-8 did not increase bleeding at the doses up to 10-fold of the effectively antithrombotic doses compared with nHG and low molecular weight heparin in the mice tail-cut model. Considering that dHG-5 possesses strong anti-iXase and antithrombotic activities, and its preparation process is simpler and its yield is higher compared with oHG-8, it might be a promising antithrombotic candidate.

MeSH terms

  • Animals
  • Anticoagulants / chemistry
  • Anticoagulants / metabolism*
  • Anticoagulants / therapeutic use*
  • Blood Coagulation
  • Cysteine Endopeptidases / chemistry
  • Cysteine Endopeptidases / metabolism*
  • Cysteine Endopeptidases / therapeutic use
  • Disease Models, Animal
  • Glycosaminoglycans / chemistry
  • Glycosaminoglycans / metabolism*
  • Glycosaminoglycans / therapeutic use
  • Hemorrhage / drug therapy*
  • Humans
  • Male
  • Mice
  • Mice, Inbred Strains
  • Neoplasm Proteins / chemistry
  • Neoplasm Proteins / metabolism*
  • Neoplasm Proteins / therapeutic use
  • Polymerization
  • Rabbits
  • Rats
  • Rats, Sprague-Dawley
  • Sea Cucumbers
  • Venous Thrombosis / drug therapy*

Substances

  • Anticoagulants
  • Glycosaminoglycans
  • Neoplasm Proteins
  • Cysteine Endopeptidases
  • cancer procoagulant