Sood Vikram, Luke Cathy, Miller Erin, Mitsuya Mayo, Upchurch Gilbert R, Wakefield Thomas W, Myers Dan D, Henke Peter K
Jobst Vascular Surgery Laboratory, Section of Vascular Surgery, University of Michigan Medical School, Ann Arbor, MI, USA.
Ann Vasc Surg. 2010 Feb;24(2):233-41. doi: 10.1016/j.avsg.2009.11.002.
Venous thrombus resolution sets up an early intense inflammatory reaction, from which vein wall damage results. Tissue response to injury includes matrix metalloproteinase (MMP) activation and extracellular matrix protein turnover. This study sought to determine the effect of exogenous MMP inhibition and its potential attenuation of early vein wall injury.
Rats received treatment beginning 24 hr after a stasis venous thrombosis by near occlusive ligation and until harvest at day 7. Three groups were evaluated: (1) vehicle saline controls (NaCl), (2) low molecular weight heparin (LMWH; Lovenox, 3 mg/kg daily SQ), and (3) doxycycline (DOXY, 30 mg/kg daily PO). Thrombus size (mg/mm), levels of tumor necrosis factor alpha (TNF alpha) and D-dimer by colorimetric assay, and monocytes counts by immunohistochemistry were assessed. Vein wall assessment included stiffness by tensiometry, interleukin 1beta (IL-1 beta protein levels by enzyme-linked immunosorbent assay, MMP2 and -9 by zymography, and histological analysis of intimal thickness (IT). Comparisons were by t-test to control. p < 0.05 was considered significant.
Thrombus sizes were similar at days 2 and 7 for all three groups, while thrombus TNFalpha was increased in 2-day LMWH- and DOXY-treated groups (NaCl = 1.0 +/- 0.8, LWMH = 9 +/- 3, DOXY = 27 +/- 5 pg/mg protein, n = 6-8, p < 0.05) and at 7 days in the DOXY group (NaCl = 3.0 +/- 2.5, DOXY = 23 +/- 4.2 pg/mg protein, n = 5, p < 0.05). Vein wall stiffness at 7 days was less with LMWH treatment, but not with DOXY, compared to controls (NaCl = 0.33 +/- 0.05, LMWH = 0.17 +/- 0.03, DOXY = 0.43 +/- 0.09 N/mm, n = 5-7, p < 0.05). Vessel-wall IL-1 beta was reduced only in the DOXY group at 7 days (NaCl = 26 +/- 3, LMWH = 38 +/- 17, DOXY = 6 +/- 3 pg/mg protein, n = 4-6, p < 0.05), as was the IT score versus controls (NaCl = 2.2 +/- 0.6, LMWH =1.7 +/- 0.3, DOXY = 0.8 +/- 0.20, n = 4-6, p < 0.05). Zymographic MMP9 activity was significantly reduced at 2 days in the LMWH and DOXY groups (NaCl = 85 +/- 24, LMWH = 23 +/- 7( *), DOXY = 13 +/- 5 U/mg protein, n = 6-8, p < 0.05). MMP2 zymographic activity, thrombus monocyte cell counts, and D-dimer activity were not significantly different across groups.
Treatment with LMWH or DOXY did not alter the size of deep vein thrombosis, mildly altered thrombus composition, and differentially affected vein wall injury, despite similar reductions in early MMP9 activity. Whether exogenous MMP inhibition affects long-term vein wall fibrosis will require further study.
静脉血栓溶解引发早期强烈的炎症反应,进而导致静脉壁损伤。组织对损伤的反应包括基质金属蛋白酶(MMP)激活和细胞外基质蛋白更新。本研究旨在确定外源性MMP抑制的效果及其对早期静脉壁损伤的潜在减轻作用。
大鼠在通过近闭塞结扎形成淤滞性静脉血栓后24小时开始接受治疗,直至第7天处死取材。评估三组:(1)赋形剂生理盐水对照组(NaCl),(2)低分子量肝素(LMWH;速碧林,每日3mg/kg皮下注射),以及(3)强力霉素(DOXY,每日30mg/kg口服)。通过比色法评估血栓大小(mg/mm)、肿瘤坏死因子α(TNFα)和D-二聚体水平,通过免疫组织化学评估单核细胞计数。静脉壁评估包括通过张力测定法评估硬度,通过酶联免疫吸附测定法评估白细胞介素1β(IL-1β)蛋白水平,通过酶谱法评估MMP2和-9,以及对内膜厚度(IT)进行组织学分析。通过t检验与对照组进行比较。p<0.05被认为具有统计学意义。
所有三组在第2天和第7天的血栓大小相似,而在第2天,LMWH和DOXY治疗组的血栓TNFα增加(NaCl = 1.0±0.8,LWMH = 9±3,DOXY = 27±5 pg/mg蛋白,n = 6 - 8,p<0.05),在第7天DOXY组的血栓TNFα也增加(NaCl = 3.0±2.5,DOXY = 23±4.2 pg/mg蛋白,n = 5,p<0.05)。与对照组相比,LMWH治疗组在第7天的静脉壁硬度降低,但DOXY组未降低(NaCl = 0.33±0.05,LMWH = 0.17±0.03,DOXY = 0.43±0.09 N/mm,n = 5 - 7,p<0.05)。仅DOXY组在第7天的血管壁IL-1β降低(NaCl = 26±3,LMWH = 38±17,DOXY = 6±3 pg/mg蛋白,n = 4 - 6,p<0.05),与对照组相比IT评分也降低(NaCl = 2.2±0.6,LMWH =1.7±0.3,DOXY = 0.8±0.20,n = 4 - 6,p<0.05)。在第2天,LMWH和DOXY组的酶谱法MMP9活性显著降低(NaCl = 85±24,LMWH = 23±7(*),DOXY = 13±5 U/mg蛋白,n = 6 - 8,p<0.05)。MMP2酶谱活性、血栓单核细胞计数和D-二聚体活性在各组之间无显著差异。
尽管早期MMP9活性有相似程度的降低,但LMWH或DOXY治疗并未改变深静脉血栓的大小,轻微改变了血栓组成,并对静脉壁损伤有不同影响。外源性MMP抑制是否会影响长期静脉壁纤维化仍需进一步研究。