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贝米肝素钠、依诺肝素钠、那屈肝素钙和亭扎肝素钠的抗血管生成活性。

Antiangiogenic activities of bemiparin sodium, enoxaparin sodium, nadroparin calcium and tinzaparin sodium.

机构信息

Department of Chest Diseases, Cumhuriyet University School of Medicine, Sivas, Turkey.

出版信息

Thromb Res. 2011 Oct;128(4):e29-32. doi: 10.1016/j.thromres.2011.05.005. Epub 2011 May 24.


DOI:10.1016/j.thromres.2011.05.005
PMID:21605890
Abstract

INTRODUCTION: The low-molecular-weight heparins have been demonstrated to have antiangiogenic effects in various assays. We aimed to demonstrate and compare the antiangiogenic effects of four types of commercially available low-molecular weight heparins in the chick embryo chorioallantoic membrane model. MATERIALS AND METHODS: The antiangiogenic efficacies of bemiparin, enoxaparin, nadroparin, and tinzaparin were examined in vivo in the chick chorioallantoic membrane model. Drug solutions are prepared in three different concentrations (100 IU, 10 IU, or 1 IU/10 μl). For each set of experiment twenty fertilized eggs were used. The decrease of vessel formation is examined and scored according to previous literature. RESULTS: Bemiparin, enoxaparin, nadroparin, and tinzaparin sodium all have antiangiogenic effects on chick chorioallantoic membrane at the concentration of 100 IU/10 μl. This effect was also observed in 10 IU/10 μl concentrations of nadroparin and tinzaparin. CONCLUSIONS: The low molecular weight heparins studied have obvious antiangiogenic effects. There may be a difference in the potency of the drugs that could have a significant implication for further clinical research.

摘要

简介:低分子量肝素已在各种检测中被证实具有抗血管生成作用。我们旨在展示和比较四种市售的低分子量肝素在鸡胚绒毛尿囊膜模型中的抗血管生成作用。

材料和方法:在鸡绒毛尿囊膜模型中体内检测贝米肝素、依诺肝素、那屈肝素和亭扎肝素的抗血管生成功效。药物溶液以三种不同浓度(100 IU、10 IU 或 1 IU/10 μl)配制。对于每组实验,使用二十个受精蛋。根据先前的文献,检查并评分血管生成的减少。

结果:贝米肝素、依诺肝素、那屈肝素和亭扎肝素钠在 100 IU/10 μl 的浓度下对鸡绒毛尿囊膜均具有抗血管生成作用。那屈肝素和亭扎肝素的 10 IU/10 μl 浓度也观察到这种作用。

结论:研究中的低分子量肝素具有明显的抗血管生成作用。药物的效力可能存在差异,这可能对进一步的临床研究具有重要意义。

相似文献

[1]
Antiangiogenic activities of bemiparin sodium, enoxaparin sodium, nadroparin calcium and tinzaparin sodium.

Thromb Res. 2011-5-24

[2]
Comparison of the antiangiogenic effects of heparin sodium, enoxaparin sodium, and tinzaparin sodium by using chorioallantoic membrane assay.

Blood Coagul Fibrinolysis. 2012-4

[3]
Investigation of the antiangiogenic behaviors of rivaroxaban and low molecular weight heparins.

Blood Coagul Fibrinolysis. 2014-6

[4]
Effects of low molecular weight heparins and unfractionated heparin on viability of human umbilical vein endothelial cells.

Arch Gynecol Obstet. 2012-9-18

[5]
Comparative pharmacodynamic assessment of the antiangiogenesis activity of heparin and low-molecular-weight heparin fractions: structure-function relationship.

Clin Appl Thromb Hemost. 2012-2-12

[6]
A study of unfractionated and low molecular weight heparins in a model of cholestatic liver injury in the rat.

Pharmacol Res. 2005-1

[7]
Influence of low molecular weight heparin preparations on human internal thoracic artery contraction.

Eur J Cardiothorac Surg. 2004-11

[8]
Comparative pharmacodynamic time-course of bemiparin and enoxaparin in healthy volunteers.

Int J Clin Pharmacol Ther. 2009-12

[9]
Effects of heparin and low-molecular-weight heparins on bone mechanical properties in rats.

Thromb Haemost. 2004-11

[10]
Microvascular effects of the low molecular weight heparins in a colorectal xenograft model: an intravital microscopy study.

J Surg Res. 2015-4

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