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The neutralization of heparan sulfate by heparin-binding copolymer as a potential therapeutic target

机译:肝素结合共聚物作为潜在治疗靶标的硫酸乙酰肝素的中和

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摘要

Besides regulating ligand-receptor and cell-cell interactions, heparan sulfate (HS) may participate in the development of many diseases, such as cancer, bacterial or viral infections, and their complications, like bleeding or inflammation. In these cases, the neutralization of HS could be a potential therapeutic target. The heparin-binding copolymer (HBC, PEG41-PMAPTAC53) was previously reported by us as a fully synthetic compound for efficient and safe neutralization of heparins and synthetic anticoagulants. In a search for molecular antagonists of HS, we examined the activity of HBC as an HS inhibitor both in vitro and in vivo and characterized HBC/HS complexes. Using a colorimetric Azure A method, isothermal titration calorimetry and dynamic light scattering techniques we found that HBC binds HS by forming complexes below 200 nm with less than 1 : 1 stoichiometry. We confirmed the HBC inhibitory effect in rats by measuring activated partial thromboplastin time, prothrombin time, anti-factor Xa activity, anti-factor IIa activity, and platelet aggregation. HBC reversed the enhancement of all tested parameters caused by HS demonstrating that cationic synthetic block copolymers may have a therapeutic value in various disorders involving overproduction of HS.
机译:除了调节配体受体和细胞 - 细胞相互作用之外,硫酸乙酰肝素(HS)可以参与许多疾病的发展,例如癌症,细菌或病毒感染,以及它们的并发症,如出血或炎症。在这些情况下,HS的中和可能是潜在的治疗目标。肝素结合的共聚物(HBC,PEG41-PMAPTAC53)先前被美国作为完全合成的化合物报道,用于高效和安全中和肝素和合成抗凝血剂。在寻找HS的分子拮抗剂中,我们将HBC作为HS抑制剂的活性在体外和体内进行,并表征HBC / HS络合物。使用比色氮杂法的方法,等温滴定热量和动态光散射技术,我们发现HBC通过在200nm以下的复合物具有小于1:1的化学计量中结合HS。通过测量活性的部分血栓形成时间,凝血酶原时间,抗因子Xa活性,抗因子IIa活性和血小板聚集,我们确认了大鼠HBC抑制作用。 HBC逆转了由HS引起的所有测试参数的增强,证明阳离子合成嵌段共聚物可能具有涉及HS过量生产的各种疾病的治疗价值。

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  • 来源
    《RSC Advances 》 |2019年第6期| 共10页
  • 作者单位

    Med Univ Bialystok Dept Pharmacodynam Mickiewicza 2c PL-15089 Bialystok Poland;

    Med Univ Bialystok Dept Pharmacodynam Mickiewicza 2c PL-15089 Bialystok Poland;

    Jagiellonian Univ Fac Chem Gronostajowa 2 PL-30387 Krakow Poland;

    Jagiellonian Univ Fac Chem Gronostajowa 2 PL-30387 Krakow Poland;

    Univ Hyogo Grad Sch Engn Dept Appl Chem Himeji Hyogo Japan;

    Med Univ Bialystok Dept Pharmacodynam Mickiewicza 2c PL-15089 Bialystok Poland;

    Jagiellonian Univ Fac Chem Gronostajowa 2 PL-30387 Krakow Poland;

    Jagiellonian Univ Fac Chem Gronostajowa 2 PL-30387 Krakow Poland;

    Med Univ Bialystok Dept Pharmacodynam Mickiewicza 2c PL-15089 Bialystok Poland;

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  • 正文语种 eng
  • 中图分类 化学 ;
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