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胺化岩藻多糖的制备及其作为抗血栓和抗血脂药物的评价。

Preparation of aminated fucoidan and its evaluation as an antithrombotic and antilipemic agent.

作者信息

Soeda S, Ohmagari Y, Shimeno H, Nagamatsu A

机构信息

Department of Biochemistry, Faculty of Pharmaceutical Sciences, Fukuoka University, Japan.

出版信息

Biol Pharm Bull. 1994 Jun;17(6):784-8. doi: 10.1248/bpb.17.784.

Abstract

Fucoidan, a sulfated poly(L-fucopyranose), is an effective anticoagulant in vitro and in vivo. In the present study, an aminated derivative of fucoidan was prepared and examined for its fibrinolytic and anticoagulant activities. The aminated derivative was more potent than native fucoidan as a stimulator of tissue plasminogen activator-induced plasma clot lysis, and its effectiveness was comparable to that of oversulfated fucoidan reported previously. Furthermore, the ability of aminated fucoidan to accelerate heparin cofactor II-mediated thrombin inhibition was 2.3 times more potent than that of native fucoidan. Aminated fucoidan effectively prevented endotoxin-induced hepatic vein thrombosis in hyperlipemic rats and decreased the elevated levels of serum cholesterol and triglyceride. The present results that the anticoagulant and antilipemic potency of fucoidan can be improved by charge modification may provide useful clues for the development of an ideal anticoagulant and antilipemic drug.

摘要

岩藻聚糖硫酸酯,一种硫酸化的聚(L-岩藻糖),在体外和体内都是一种有效的抗凝剂。在本研究中,制备了岩藻聚糖硫酸酯的胺化衍生物,并检测了其纤溶和抗凝活性。作为组织纤溶酶原激活剂诱导的血浆凝块溶解的刺激剂,胺化衍生物比天然岩藻聚糖硫酸酯更有效,其有效性与先前报道的过度硫酸化岩藻聚糖硫酸酯相当。此外,胺化岩藻聚糖硫酸酯加速肝素辅因子II介导的凝血酶抑制的能力比天然岩藻聚糖硫酸酯强2.3倍。胺化岩藻聚糖硫酸酯有效预防了高脂血症大鼠内毒素诱导的肝静脉血栓形成,并降低了血清胆固醇和甘油三酯的升高水平。岩藻聚糖硫酸酯的抗凝和抗血脂效力可通过电荷修饰得到改善,目前的这些结果可能为开发理想的抗凝和抗血脂药物提供有用的线索。

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