Myers Daniel D, Henke Peter K, Wrobleski Shirley K, Hawley Angela E, Farris Diana M, Chapman Amy M, Knipp Brian S, Thanaporn Porama, Schaub Robert G, Greenfield Lazar J, Wakefield Thomas W
Section of Vascular Surgery, Department of Surgery, Jobst Vascular Laboratory, Ann Arbor, MI 48109, USA.
J Vasc Surg. 2002 Nov;36(5):928-38. doi: 10.1067/mva.2002.128636.
The purpose of this study was to compare the efficacy of P-selectin inhibition with standard anticoagulant and thrombolytic therapy in a rodent model of established deep vein thrombosis (DVT).
Rats underwent temporary inferior vena cava (IVC) ligation for 2 days to create a stasis-induced thrombosis. On day 2, the animals had the IVC ligature removed and received either recombinant P-selectin glycoprotein ligand-Ig (rPSGL-Ig; 4 mg/kg) intravenously, low-molecular weight heparin (LMWH; 450 IU/kg) subcutaneously, tissue plasminogen activator (tPA; 0.5 mg/kg) intravenously, combination rPSGL-Ig plus tPA, or saline vehicle. IVC segments were harvested from rats at 4 (n = 8) and 7 (n = 3) days after treatment. All treatments were given as a single dose except for daily LMWH. Evaluation included contrast venography with computer image analysis, thrombus weight/length (mass), vein wall leukocyte counts, cytokine and tissue factor analysis with enzyme-linked immunosorbent assay, and (ED1) monocyte immunohistochemical staining. Collagen was estimated with a quantitative assay.
Contrast venography revealed that rats with both rPSGL-Ig and tPA treatment had significantly smaller thrombi as compared with controls at day 7 (0.34 +/- 0.07 cm(2) and 0.34 +/- 0.05 cm(2) versus 0.68 +/- 0.13 cm(2); P <.05). LMWH and tPA groups had significantly decreased thrombus mass at harvest compared with controls on day 4 (0.06 +/- 0.009 g/cm and 0.08 +/- 0.01 g/cm versus 0.1 +/- 0.005 g/cm; P <.05), and rPSGL-Ig showed a similar trend (P =.072). Vein wall, but not thrombus, monocytes were more numerous in those rats receiving rPSGL-Ig versus controls at day 4 (30 +/- 4 cells/5 high power fields [HPFs] versus 19 +/- 2 cells/5 HPFs; P <.05) and at day 7 (32 +/- 2 cells/5 HPFs versus 20 +/- 3 cells/5 HPFs; P <.05). rPSGL-Ig treatment was associated with significantly reduced vein wall collagen at day 7 versus controls (1.3 +/- 0.6 pg/mg versus 3.7 +/- 0.5 pg/mg; P <.05) and a trend toward lower tissue factor levels.
rPSGL-Ig, LMWH, and tPA showed equal DVT resolution efficacy over 7 days. However, only rPSGL-Ig was associated with a decrease in vein wall fibrosis, suggesting that purely accelerating DVT resolution may not decrease long-term vein scarring.
本研究旨在比较在已建立的深静脉血栓形成(DVT)啮齿动物模型中,P-选择素抑制与标准抗凝和溶栓治疗的疗效。
大鼠接受下腔静脉(IVC)临时结扎2天以形成淤滞诱导的血栓形成。在第2天,移除动物的IVC结扎线,并静脉内给予重组P-选择素糖蛋白配体-Ig(rPSGL-Ig;4mg/kg)、皮下给予低分子量肝素(LMWH;450IU/kg)、静脉内给予组织纤溶酶原激活剂(tPA;0.5mg/kg)、rPSGL-Ig加tPA联合用药或生理盐水载体。在治疗后4天(n = 8)和7天(n = 3)从大鼠采集IVC节段。除每日LMWH外,所有治疗均给予单次剂量。评估包括计算机图像分析的造影静脉造影、血栓重量/长度(质量)、静脉壁白细胞计数、酶联免疫吸附测定的细胞因子和组织因子分析以及(ED1)单核细胞免疫组织化学染色。用定量测定法估计胶原蛋白。
造影静脉造影显示,与对照组相比,在第7天接受rPSGL-Ig和tPA治疗的大鼠血栓明显更小(分别为0.34±0.07cm²和0.34±0.05cm²,而对照组为0.68±0.13cm²;P<.05)。与对照组相比,LMWH组和tPA组在收获时血栓质量在第4天显著降低(分别为0.06±0.009g/cm和0.08±0.01g/cm,而对照组为0.1±0.005g/cm;P<.05),rPSGL-Ig显示出类似趋势(P = 0.072)。在第4天(30±4个细胞/5个高倍视野[HPFs]对19±2个细胞/5个HPFs;P<.05)和第7天(32±2个细胞/5个HPFs对20±3个细胞/5个HPFs;P<.05),接受rPSGL-Ig治疗的大鼠静脉壁而非血栓中的单核细胞数量比对照组更多。与对照组相比,rPSGL-Ig治疗在第7天与静脉壁胶原蛋白显著减少相关(1.3±0.6pg/mg对3.7±0.5pg/mg;P<.05),并且组织因子水平有降低趋势。
rPSGL-Ig、LMWH和tPA在7天内显示出同等的DVT溶解疗效。然而,只有rPSGL-Ig与静脉壁纤维化减少相关,这表明单纯加速DVT溶解可能不会减少长期静脉瘢痕形成。