Literature DB >> 19399370

M118, a novel low-molecular weight heparin with decreased polydispersity leads to enhanced anticoagulant activity and thrombotic occlusion in ApoE knockout mice.

Subrata Chakrabarti1, Lea M Beaulieu, Lara A Reyelt, Mark D Iafrati, Jane E Freedman.   

Abstract

Heparin and low-molecular weight heparin (LMWH) are complex, heterogeneous polysaccharides used in the treatment of arterial and venous thrombosis. M118 is a novel LMWH with low polydispersity and pronounced anti-Xa and anti-thrombin (IIa) activity as compared to current LMWHs. To determine if M118 is effective in preventing thrombosis in the setting of a vascular plaque, apolipoprotein E knockout mice fed a high fat diet were injected with M118, enoxaparin, unfractionated heparin, or saline control and examined for arterial thrombosis using a rose bengal laser induced carotid artery injury model. M118 significantly increased the time to occlusion as compared to control and unfractionated heparin but not compared to enoxaparin although fewer M118 treated animals had any vascular occlusion present at the time of protocol completion. Platelet-neutrophil aggregates were studied by flow cytometry and were found to be decreased with M118 as compared to enoxaparin. This is the first published report examining M118, a novel LMWH designed to have low polydispersity and enhanced anticoagulant activity. In an animal model of vascular plaque, M118 is a potent inhibitor of arterial thrombosis and, despite lower in vivo anti-Xa and anti-IIa activity levels, M118 was superior to UFH in the prevention of arterial thrombosis.

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Year:  2009        PMID: 19399370      PMCID: PMC2826881          DOI: 10.1007/s11239-009-0340-4

Source DB:  PubMed          Journal:  J Thromb Thrombolysis        ISSN: 0929-5305            Impact factor:   2.300


  25 in total

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Review 2.  Preventing venous thromboembolism in general medical inpatients and after an ischaemic stroke.

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Journal:  Haemostasis       Date:  2000

3.  Leukocyte-platelet aggregation, platelet surface P-selectin, and platelet surface glycoprotein IIIa after percutaneous coronary intervention: Effects of dalteparin or unfractionated heparin in combination with abciximab.

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4.  Automated selection of DAB-labeled tissue for immunohistochemical quantification.

Authors:  Eric M Brey; Zahid Lalani; Carol Johnston; Mark Wong; Larry V McIntire; Pauline J Duke; Charles W Patrick
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5.  Variable protection of beta 3-integrin--deficient mice from thrombosis initiated by different mechanisms.

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6.  Circulating monocyte-platelet aggregates are a more sensitive marker of in vivo platelet activation than platelet surface P-selectin: studies in baboons, human coronary intervention, and human acute myocardial infarction.

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7.  Cleavage of the antithrombin III binding site in heparin by heparinases and its implication in the generation of low molecular weight heparin.

Authors:  Z Shriver; M Sundaram; G Venkataraman; J Fareed; R Linhardt; K Biemann; R Sasisekharan
Journal:  Proc Natl Acad Sci U S A       Date:  2000-09-12       Impact factor: 11.205

8.  Circulating monocyte-platelet aggregates are an early marker of acute myocardial infarction.

Authors:  M I Furman; M R Barnard; L A Krueger; M L Fox; E A Shilale; D M Lessard; P Marchese; A L Frelinger; R J Goldberg; A D Michelson
Journal:  J Am Coll Cardiol       Date:  2001-10       Impact factor: 24.094

9.  Neutrophil CD40 enhances platelet-mediated inflammation.

Authors:  Pantila Vanichakarn; Price Blair; Cindy Wu; Jane E Freedman; Subrata Chakrabarti
Journal:  Thromb Res       Date:  2008-03-04       Impact factor: 3.944

10.  Rational design of low-molecular weight heparins with improved in vivo activity.

Authors:  Mallik Sundaram; Yiwei Qi; Zachary Shriver; Dongfang Liu; Ganlin Zhao; Ganesh Venkataraman; Robert Langer; Ram Sasisekharan
Journal:  Proc Natl Acad Sci U S A       Date:  2003-01-13       Impact factor: 11.205

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