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首页> 外文期刊>Thrombosis Research: An International Journal on Vascular Obstruction, Hemorrhage and Hemostasis >Endogenous release of tissue factor pathway inhibitor by topical application of an ointment containing mucopolysaccharide polysulfate to nonhuman primates.
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Endogenous release of tissue factor pathway inhibitor by topical application of an ointment containing mucopolysaccharide polysulfate to nonhuman primates.

机译:通过向非人类灵长类动物局部应用含有粘多糖多硫酸盐的药膏内源性释放组织因子途径抑制剂。

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摘要

Several studies have shown that tissue factor pathway inhibitor (TFPI) is released after the intravenous and subcutaneous administration of heparin and heparin-related drugs. Mucopolysaccharide polysulfate (MPS) is a preparation of glycosaminoglycans (GAGS) derived from mammalian cartilage, which has several structural and functional properties similar to heparin. Previous reports have shown that MPS is capable of releasing TFPI after intravenous administration. Therefore, this investigation was performed to determine the ability of topically administered MPS to release TFPI in a nonhuman primate model. A group of four monkeys were administered 3% MPS ointment in a dosage of 0.5 g/kg corresponding to 15 mg MPS/kg; another four monkeys were administered placebo ointment at a dosage of 0.5 g/kg once a day for 5 days in a period of 10 days. No effect of MPS was observed on the coagulation assays activated partial thromboplastin time (APTT), thrombin time (TT) and Heptest or on the platelet count. However,both the total and free TFPI levels were significantly and progressively elevated over the 10-day period in comparison to the placebo control group (P<.05). It is proposed that the ability of the topically administered MPS to increase the free and total TFPI levels may be one of the modes of action that contributes to the anticoagulant and anti-inflammatory actions of this agent.
机译:几项研究表明,静脉注射和皮下注射肝素及肝素相关药物后,组织因子途径抑制剂(TFPI)被释放。粘多糖多硫酸盐(MPS)是衍生自哺乳动物软骨的糖胺聚糖(GAGS)的制剂,其具有与肝素相似的几种结构和功能特性。先前的报道表明,MPS能够在静脉内给药后释放TFPI。因此,进行该研究以确定在非人灵长类动物模型中局部施用的MPS释放TFPI的能力。一组四只猴子以0.5 g / kg的剂量(相当于15 mg MPS / kg)施用3%MPS软膏;在10天内,每天以0.5 g / kg的剂量给另外四只猴子施用一次安慰剂软膏,持续5天。在凝血测定,活化的部分凝血活酶时间(APTT),凝血酶时间(TT)和Heptest或血小板计数方面,未观察到MPS的影响。然而,与安慰剂对照组相比,在10天内,总TFPI和游离TFPI的水平均显着且逐渐升高(P <.05)。提出局部施用的MPS增加游离和总TFPI水平的能力可能是有助于该剂的抗凝和抗炎作用的作用方式之一。

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