In vivo antithrombotic synergy of oral heparin and arginine:: Endothelial thromboresistance without changes in coagulation parameters

被引:8
作者
Daniels, Bruce
Linhardt, Robert J.
Zhang, Fuming
Ma, Wenjun
Wice, Sandra M.
Hiebert, Linda M.
机构
[1] Rensselaer Polytech Inst, Biotechnol Ctr 4005, Dept Chem & Chem Biol Biol & Chem & Biol Engn, Troy, NY 12180 USA
[2] Qingdao Ocean Univ, Ctr Marine Foods & Drugs, Qingdao, Peoples R China
[3] Univ Saskatchewan, Dept Vet Biomed Sci, Saskatoon, SK, Canada
关键词
heparin; thrombosis; endothelium; arginine; oral;
D O I
10.1160/TH05-12-0786
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
On the basis of suggested clinical efficacy in an uncontrolled study in ninety-seven patients with unstable angina, an animal study was conducted to investigate antithrombotic synergy between orally administered heparin and arginine. A rat venous thrombosis model tested the difference in thrombus formation when heparin (7.5 mg/kg) and arginine (113 mg/kg) were administered, alone or in combination, by stomach tube with a minimum of 20 rats/group. Oral heparin, arginine, and heparin plus arginine reduced thrombus formation by 50%, 75%, and 90%, respectively,when compared to saline administration. Heparin was recovered from endothelium, yet there was little or no observable plasma anticoagulant activity. An orally administered low-molecular-weight anticoagulant glycosaminoglycan mixture, sulodexide (7.5 mg/kg), showed an 88% reduction in stable thrombus formation when administered alone but showed no synergy with oral arginine. A 28-day study with oral sulodexide (2.9 mg/kg) and arginine (43.9 mg/kg), 20 rats/group, showed antithrombotic activity with minimal anticoagulant activity indicating suitability for long term treatment. These findings suggest the endothelial localization of heparin and a synergistic antithrombotic effect for orally administered heparin and arginine.
引用
收藏
页码:865 / 872
页数:8
相关论文
共 37 条
[1]   Regulation of P-selectin expression in human endothelial cells by nitric oxide [J].
Armstead, VE ;
Minchenko, AG ;
Schuhl, RA ;
Hayward, R ;
Nossuli, TO ;
Lefer, AM .
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 1997, 273 (02) :H740-H746
[2]   Expression of heparan sulphate N-deacetylase/N-sulphotransferase by vascular smooth muscle cells [J].
Bingley, JA ;
Hayward, IP ;
Girjes, AA ;
Campbell, GR ;
Humphries, DE ;
Stow, JL ;
Campbell, JH .
HISTOCHEMICAL JOURNAL, 2002, 34 (3-4) :131-137
[3]   AN ASSAY FOR THE ANTITHROMBOTIC ACTIVITY OF ANTICOAGULANTS [J].
BLAKE, OR ;
ASHWIN, JG ;
JAQUES, LB .
JOURNAL OF CLINICAL PATHOLOGY, 1959, 12 (02) :118-122
[4]   Apoptotic vascular endothelial cells become procoagulant [J].
Bombeli, T ;
Karsan, A ;
Tait, JF ;
Harlan, JM .
BLOOD, 1997, 89 (07) :2429-2442
[5]   Endothelial cell glycocalyx modulates immobilization of leukocytes at the endothelial surface [J].
Constantinescu, AA ;
Vink, H ;
Spaan, JAE .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2003, 23 (09) :1541-1547
[6]   Modulations of glypican-1 heparan sulfate structure by inhibition of endogenous polyamine synthesis -: Mapping of spermine-binding sites and heparanase, heparin lyase, and nitric oxide/nitrite cleavage sites [J].
Ding, K ;
Sandgren, S ;
Mani, K ;
Belting, M ;
Fransson, LÅ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (50) :46779-46791
[7]   Orally ingested heparin is absorbed in humans [J].
Engelberg, H .
CLINICAL AND APPLIED THROMBOSIS-HEMOSTASIS, 1995, 1 (04) :283-285
[8]   Heparan sulfate proteoglycan is a mechanosensor on endothelial cells [J].
Florian, JA ;
Kosky, JR ;
Ainslie, K ;
Pang, ZY ;
Dull, RO ;
Tarbell, JM .
CIRCULATION RESEARCH, 2003, 93 (10) :E136-E142
[9]   DIFFERENCES IN THE INTERACTION OF HEPARIN WITH ARGININE AND LYSINE AND THE IMPORTANCE OF THESE BASIC-AMINO-ACIDS IN THE BINDING OF HEPARIN TO ACIDIC FIBROBLAST GROWTH-FACTOR [J].
FROMM, JR ;
HILEMAN, RE ;
CALDWELL, EEO ;
WEILER, JM ;
LINHARDT, RJ .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1995, 323 (02) :279-287
[10]  
Hiebert Linda M, 2002, Clin Lab, V48, P111