E-selectin inhibition with GMI-1271 decreases venous thrombosis without profoundly affecting tail vein bleeding in a mouse model

被引:34
作者
Culmer, Dorian L. [1 ]
Dunbar, Misha L. [2 ]
Hawley, Angela E. [3 ]
Sood, Suman [4 ]
Sigler, Robert E. [5 ]
Henke, Peter K. [3 ]
Wakefield, Thomas W. [3 ]
Magnani, John L. [6 ]
Myers, Daniel D., Jr. [3 ,5 ]
机构
[1] Childrens Hosp Philadelphia, Philadelphia, PA 19104 USA
[2] Univ Minnesota, Res Anim Resources, Minneapolis, MN USA
[3] Univ Michigan, Sch Med, Dept Surg, Vasc Surg, Ann Arbor, MI USA
[4] Univ Michigan, Sch Med, Div Hematol Oncol, Ann Arbor, MI USA
[5] Univ Michigan, Sch Med, Unit Lab Anim Med, Ann Arbor, MI USA
[6] GlycoMimetics Inc, Rockville, MD USA
关键词
E-selectin inhibition; glycomimetic; venous thrombosis; animal models; inflammation; CONTINUOUS BLOOD-FLOW; SOLUBLE P-SELECTIN; INFERIOR VENA-CAVA; ADHESION; THROMBOGENESIS; NEUTROPHILS; RESOLUTION; MICROPARTICLES; INFLAMMATION; DIAGNOSIS;
D O I
10.1160/TH16-04-0323
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Selectins, such as E-selectin (CD62E), function in venous thrombosis by binding and activating immune cells to initiate the coagulation cascade. GMI-1271 is a small molecule antagonist that inhibits E-selectin activity. Here we determine whether inhibition of E-selectin is sufficient to decrease acute venous thrombosis and associated inflammatory events in both prophylactic and treatment protocols without significantly affecting haemostasis. Male C57BL/6 mice underwent surgery for experimental thrombosis induction and were harvested at peak thrombus formation in our animal model, two days post induction. Groups included non-thrombosed true controls, shams, controls, and prophylactic or treatment groups of GMI-1271 (10 mg/kg intraperitoneal BID (twice a day) and low-molecular-weight heparin (LMWH, Lovenox 6 mg/kg subcutaneously (SC), once a day (SID). Compared with control animals, prophylaxis or treatment with LMWH and GMI-1271 in a dose-dependent manner significantly decreased thrombosis. GMI-1271 significantly lowered tail bleeding times when compared to LMWH. GMI-1271 and LMWH prophylactically administered significantly decreased vein wall neutrophil cell extravasation. However, all, treatment and prophylactic therapies significantly decreased vein wall monocyte extravasation versus controls. GMI-1271 prophylactic therapy significantly decreased intra-thrombus cell counts versus control animals and other treatment groups. Immunohistochemistry confirmed that both treatments with GMI-1271 and LMWH significantly decreased activated leukocyte migration. GMI-1271 therapy significantly decreased thrombus weight and resulted in significantly lower bleeding times than LMWH. GMI-1271 treated mice showed decreased local and systemic inflammatory effects while modulating neutrophil activation, suggesting that GMI-1271 is a viable therapeutic candidate for venous thrombosis prophylaxis and treatment.
引用
收藏
页码:1171 / 1181
页数:11
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