人体伤口愈合过程中皮下组织中的胶原沉积:模型评估。

APMIS. Supplementum Pub Date : 2003-01-01
Lars Nannestad Jørgensen
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引用次数: 0

摘要

伤口愈合包括凝血、炎症、血管生成、纤维增生、收缩、上皮化和重塑。在皮肤、腹壁或胃肠道等组织切开后产生肉芽组织,伤口的强度主要由愈合过程早期的胶原蛋白含量决定。很少有模型可用于研究人体伤口愈合。经皮将膨胀的聚四氟乙烯管(ePTFE)插入皮下组织已经建立了20年的模型。手术是在局部麻醉下进行的。该模型直径为2.5 mm,长度为5-10 cm,孔径为90-120微米,比血管移植物大得多。聚合物积聚肉芽组织,其结构类似于正常的外科伤口。本文对ePTFE模型在创面愈合研究中的应用进行了综述。对模型中沉积的肉芽组织进行组织学和免疫组织化学分析。肉芽组织水解后的氨基酸含量采用分光光度法或高效液相色谱法测定。模型中积累的胶原量以每ePTFE长度或每总蛋白的羟脯氨酸表示。在对老鼠进行研究之后,我们对85名健康志愿者和158名外科病人进行了研究。羟基脯氨酸含量在植入10天后高于植入5天后,且人与人之间存在较大差异。关于中位数,在同一个人的两根不同的ePTFE管上进行的两次测量之间存在25%的差异,从同一ePTFE的两个不同片段获得的值之间存在12%的差异。较高的羟脯氨酸积累水平并未导致较高的变异性。模型中脯氨酸的沉积与总蛋白含量密切相关。比较ePTFE和改良PVA模型在手术患者中的应用。与ePTFE模型相反,PVA模型没有获得羟脯氨酸沉积的可重复性测量。由此可见,改良后的PVA模型不适用于皮下肉芽组织中胶原沉积的测定。我们发现,在同一例患者中,ePTFE模型分别放置在手臂皮下组织和腹股沟无并发症的手术伤口中,胶原沉积水平之间没有相关性。手术创面胶原沉积水平明显增高。相反,在这两个位点获得的蛋白质沉积水平之间存在显著的相关性。在手臂皮下组织胶原沉积方面,接受小手术(腹股沟疝修复)的患者与健康的非创伤志愿者没有什么不同,而接受大手术的患者在术后阶段与术前评估相比,胶原沉积明显下降。这种下降在有感染并发症的患者中更为明显。研究发现,不吸烟的志愿者比年龄和性别匹配的吸烟者积累了更多的胶原蛋白(中位数82%)。不管吸烟与否,女性在模型中积累的胶原蛋白明显多于男性。这些发现在一个前瞻性的系列中被重新测试,得出了同样的结论。术后24、48 h取疝切开术创面皮下腔创液,测定基质金属蛋白酶(MMP-2、MMP-9)含量。24 h后的MMP-9与ePTFE管在创面植入后10天的胶原积累水平呈显著负相关。最后,研究表明,在ePTFE模型植入过程中,局部应用粒细胞-巨噬细胞集落刺激因子特异性和剂量依赖性地减少了成纤维细胞的数量和胶原的沉积。为实验选择的剂量产生了局部和全身效应。结论:微创ePTFE模型尽管存在一定程度的可变性,但目前仍是评估志愿者和患者在各种条件下伤口愈合潜力的最佳可能性之一。我们发现该模型便于评估伤口愈合过程中的基质沉积以及包括人口统计学特征、创伤、吸烟、药物和伤口组织降解成分在内的几个因素的影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Collagen deposition in the subcutaneous tissue during wound healing in humans: a model evaluation.

Wound healing encompasses coagulation, inflammation, angiogenesis, fibroplasia, contraction, epithelialisation and remodeling. A granulation tissue is produced following incision of tissue such as skin, abdominal wall or the gastrointestinal tract, and the strength of the wound is determined primarily by the collagen content early in the healing course. Few models are available to study wound healing in man. The percutaneous insertion of expanded poly-tetrafluoroethylene tubes (ePTFE) into the subcutaneous tissue has been an established model for 20 years. The procedure is performed using a local anesthesia. The model has a diameter of 2.5 mm, a length of 5-10 cm and a pore size of 90-120 microns which is substantially more than that of vascular grafts. The polymer accumulates granulation tissue, the architecture of which resembles that of a normal surgical wound. Previous studies on the use of the ePTFE model in wound healing research are summarized in detail. Histological and immunohistochemical analyses of the granulation tissue deposited in the model were undertaken. The content of amino acids following hydrolysis of the granulation tissue was determined applying spectrophotometric or HPLC assays. Collagen amounts accumulated in the model are expressed as hydroxyproline per length of ePTFE or per total protein. Following a study in rats we examined 85 healthy volunteers and 158 surgical patients in the studies. Higher contents of hydroxyproline were found 10 days after implantation as compared to 5 days with considerable inter-person variation. Regarding median values there was a 25% difference between two measurements performed on two distinct ePTFE tubes from the same person, and a 12% difference between values obtained from two different pieces of the same ePTFE. Higher accumulation levels of hydroxyproline did not result in higher variability. Deposition of proline in the model correlated closely to total protein content. The ePTFE and a modified PVA model were compared in surgical patients. No reproducible measurements of hydroxyproline deposition were obtained with the PVA model as opposed to the ePTFE model. It is concluded that the modified PVA model is inadequate for determination of collagen deposition in subcutaneous granulation tissue. We found no correlation between collagen deposition levels obtained with placement of the ePTFE model in the subcutaneous tissue of the arm and in an uncomplicated surgical wound of the groin in the same patient, respectively. Significantly higher collagen deposition levels in the model were found in the surgical wound. Conversely, there was a significant correlation between protein deposition levels obtained at the two sites. Patients undergoing minor surgery (groin hernia repair) did not differ from healthy non-traumatized volunteers as regards deposition of collagen in subcutaneous tissue of the arm, whereas patients subjected to major general surgery demonstrated a significant decline during the postoperative phase compared to a preoperative evaluation. This decline was enhanced in patients who had infectious complications. Non-smoking volunteers were found to specifically accumulate more collagen (median value 82%) than smokers matched for age and gender. Irrespective of the smoking status women accumulated significantly more collagen in the model than men. These findings were re-tested in a prospective series leading to the same conclusion. Matrix metalloproteinases (MMP-2 and MMP-9) were determined in wound fluid obtained from the subcutaneous cavities of herniotomy wounds 24 and 48 h after operation. A significant and inverse correlation was demonstrated between MMP-9 after 24 h and accumulation levels of collagen in the ePTFE tube 10 days after implantation in the wound. Finally, it was demonstrated that local application of granulocyte-macrophage colony-stimulating factor into the ePTFE model during implantation specifically and dose-dependently reduced the number of fibroblasts and deposition of collagen. The doses chosen for the experiments resulted in both a local and a systemic effect. It is concluded that the minimally invasive ePTFE model, despite a certain level of variability, presently provides one of the best possibilities of evaluation of the wound healing potential in both volunteers and patients under various conditions. We found the model convenient for the assessment of both matrix deposition during wound healing and the influence of several factors including demographic characteristics, trauma, tobacco smoking, drugs and tissue degrading components of the wound.

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