• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

肝素、鱼精蛋白和聚凝胺对凝血酶生成时间积分(内源性凝血酶潜力)的影响。

Influence of heparin, protamine and polybrene on the time integral of thrombin generation (endogenous thrombin potential).

作者信息

Rotteveel R C, Roozendaal K J, Weijers R N, Eijsman L

机构信息

Department of Clinical Chemistry, Onze Lieve Vrouwe Gasthuis, Amsterdam, The Netherlands.

出版信息

Haemostasis. 1996 Jan-Feb;26(1):1-10. doi: 10.1159/000217181.

DOI:10.1159/000217181
PMID:8698272
Abstract

We investigated the anticoagulating and heparin-neutralizing properties of protamine and polybrene (hexadimethrine bromide), using the endogenous thrombin potential (ETP) as the parameter to access plasma coagulability. The hypocoagulability induced by high doses of heparin (3 IU/ml) could be reversed by addition of protamine to a very limited extent only. Polybrene on the other hand did neutralize heparin at the equivalent concentration and a two-fold excess did not influence the ETP parameters. In vivo neutralization of high-dose heparin with protamine should therefore be reconsidered. Our experiments suggest polybrene to be superior over protamine with respect to neutralization of high doses of heparin.

摘要

我们使用内源性凝血酶潜力(ETP)作为评估血浆凝固性的参数,研究了鱼精蛋白和聚凝胺(溴化六烃季铵)的抗凝和中和肝素的特性。高剂量肝素(3 IU/ml)诱导的低凝性仅在非常有限的程度上可通过添加鱼精蛋白来逆转。另一方面,聚凝胺在等效浓度下确实能中和肝素,且两倍过量的聚凝胺不会影响ETP参数。因此,应重新考虑在体内用鱼精蛋白中和高剂量肝素的做法。我们的实验表明,在中和高剂量肝素方面,聚凝胺优于鱼精蛋白。

相似文献

1
Influence of heparin, protamine and polybrene on the time integral of thrombin generation (endogenous thrombin potential).肝素、鱼精蛋白和聚凝胺对凝血酶生成时间积分(内源性凝血酶潜力)的影响。
Haemostasis. 1996 Jan-Feb;26(1):1-10. doi: 10.1159/000217181.
2
In vitro neutralization of heparin in plasma prior to the activated partial thromboplastin time test: an assessment of four heparin antagonists and two anion exchange resins.
Thromb Res. 1986 Jan 1;41(1):43-56. doi: 10.1016/0049-3848(86)90278-1.
3
Protamine reversal of heparin affects platelet aggregation and activated clotting time after cardiopulmonary bypass.鱼精蛋白逆转肝素对体外循环后血小板聚集和活化凝血时间有影响。
Anesth Analg. 1998 Oct;87(4):781-5. doi: 10.1097/00000539-199810000-00008.
4
The nature of the anticoagulant effect of heparin, protamine, polybrene and toluidine blue.肝素、鱼精蛋白、聚凝胺和甲苯胺蓝的抗凝作用性质。
Scand J Clin Lab Invest. 1962;14:267-76.
5
Neutralization of low molecular weight heparin by polybrene prevents thromboxane release and severe pulmonary hypertension in awake sheep.鱼精蛋白对低分子量肝素的中和作用可防止清醒绵羊体内血栓素释放及严重肺动脉高压。
Circulation. 1990 Nov;82(5):1754-64. doi: 10.1161/01.cir.82.5.1754.
6
Thrombin generation assays are superior to traditional tests in assessing anticoagulation reversal in vitro.凝血酶生成试验在体外评估抗凝逆转方面优于传统检测方法。
Thromb Haemost. 2008 Aug;100(2):350-5.
7
A comparison of two heparin-neutralizing agents: protamine and polybrene.两种肝素中和剂的比较:鱼精蛋白和聚凝胺。
Scand J Clin Lab Invest. 1960;12(4):446-57. doi: 10.3109/00365516009065409.
8
Neutralization of dermatan sulfate in vitro and in vivo by protamine sulfate and polybrene.
Thromb Res. 1989 Apr 1;54(1):63-74. doi: 10.1016/0049-3848(89)90337-x.
9
Reversible inhibition by protamine of human synovial and rabbit platelet secretory phospholipase A2.
Biochim Biophys Acta. 1996 May 20;1300(3):226-32. doi: 10.1016/0005-2760(96)00019-7.
10
Comparative study of polybrene and protamine for heparin neutralization in open heart surgery.心脏直视手术中鱼精蛋白与聚凝胺中和肝素的对比研究。
Ann Surg. 1960 Jan;151(1):11-6.

引用本文的文献

1
Reassessment of dextran sulfate in anti-Xa assay for unfractionated heparin laboratory monitoring.硫酸葡聚糖在普通肝素实验室监测抗Xa检测中的重新评估。
Res Pract Thromb Haemost. 2023 Nov 9;7(8):102257. doi: 10.1016/j.rpth.2023.102257. eCollection 2023 Nov.
2
Discovery of allosteric modulators of factor XIa by targeting hydrophobic domains adjacent to its heparin-binding site.通过靶向因子 XIa 肝素结合位点相邻的疏水结构域发现别构调节剂。
J Med Chem. 2013 Mar 28;56(6):2415-28. doi: 10.1021/jm301757v. Epub 2013 Mar 18.
3
Inhibition of polyphosphate as a novel strategy for preventing thrombosis and inflammation.
聚磷酸盐抑制作为一种预防血栓和炎症的新策略。
Blood. 2012 Dec 20;120(26):5103-10. doi: 10.1182/blood-2012-07-444935. Epub 2012 Sep 11.