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实验性抗血栓形成剂去纤苷对人体纤溶和血中前列腺素的急性作用。

Acute effects of defibrotide, an experimental antithrombotic agent, on fibrinolysis and blood prostanoids in man.

作者信息

Coccheri S, Biagi G, Legnani C, Bianchini B, Grauso F

机构信息

Chair of Medical Pathophysiology, University Hospital S. Orsola, Bologna, Italy.

出版信息

Eur J Clin Pharmacol. 1988;35(2):151-6. doi: 10.1007/BF00609244.

Abstract

Defibrotide is a polynucleotide extracted from mammalian lung, which shows antithrombotic and anti-ischaemic activity in animals, probably related to stimulation of fibrinolysis and/or enhancement of prostacyclin production. The effect of a single infusion of defibrotide on fibrinolysis and the levels of certain prostanoids in man has been investigated in a cross-over double-blind placebo-controlled study. Evaluation of changes in fibrinolysis was difficult because of the spontaneous activation observed after placebo. However, the fast-acting plasminogen activator inhibitor was decreased only at end of the defibrotide infusion, suggesting a moderate profibrinolytic effect superimposed on the spontaneous activation. There was a marked and prolonged elevation of the plasma level of 6-keto-PGF1 alpha, the stable metabolite of prostacyclin. In collagen stimulated whole blood, both 6-keto-PGF1 alpha and prostaglandin E2 production were also greatly increased, with no consistent indication of inhibition of thromboxane B2. It is suggested that defibrotide stimulates prostacyclin and prostaglandin E2 production by leucocytes or via platelet/leukocyte interactions. The effects observed here should be useful in guiding subsequent clinical trials.

摘要

去纤苷是一种从哺乳动物肺中提取的多核苷酸,在动物中显示出抗血栓形成和抗缺血活性,这可能与刺激纤维蛋白溶解和/或增强前列环素生成有关。在一项交叉双盲安慰剂对照研究中,研究了单次输注去纤苷对人体纤维蛋白溶解和某些前列腺素水平的影响。由于安慰剂后观察到自发激活,因此评估纤维蛋白溶解的变化很困难。然而,快速作用的纤溶酶原激活物抑制剂仅在去纤苷输注结束时降低,这表明在自发激活的基础上有适度的促纤维蛋白溶解作用。前列环素的稳定代谢产物6-酮-前列腺素F1α的血浆水平有明显且持久的升高。在胶原刺激的全血中,6-酮-前列腺素F1α和前列腺素E2的生成也大大增加,没有一致的迹象表明血栓素B2受到抑制。提示去纤苷可通过白细胞或通过血小板/白细胞相互作用刺激前列环素和前列腺素E2的生成。这里观察到的效应应该有助于指导后续的临床试验。

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