Mattsby-Baltzer I, Jakobsson A, Sörbo J, Norrby K
Department of Clinical Bacteriology, University of Göteborg, Sweden.
Int J Exp Pathol. 1994 Jun;75(3):191-6.
The formation of new blood vessels, angiogenesis, is an important event in inflammation, wound healing and tumour growth. Mediators produced by various cells when exposed to endotoxin include cytokines (tumour necrosis factor, interleukins 1 and 6, and basic fibroblast growth factor) which, it has been suggested, stimulate angiogenesis. The angiogenic effect of endotoxin (lipopolysaccharide, LPS) was studied in rats using the quantitative mesenteric window assay. Adult rats were injected intraperitoneally with Escherichia coli LPS (5 pg/ml-20,000 ng/ml) twice daily for 4.5 consecutive days and were sacrificed 14 days after the start of this treatment. An angiogenic response was observed at concentrations of > 2 ng/ml in a dose-dependent manner. No inflammatory cellular exudate was seen in the test tissue at the time of angiogenesis analysis. Suppressed body-weight gain, a marker of the systemic effect of LPS in the rat, was significant only at the highest dose tested. The data suggest that endotoxin-mediated neovascularization could be a component of inflammation and wound healing.
新血管的形成,即血管生成,是炎症、伤口愈合和肿瘤生长过程中的一个重要事件。各种细胞在接触内毒素时产生的介质包括细胞因子(肿瘤坏死因子、白细胞介素1和6以及碱性成纤维细胞生长因子),有人认为这些细胞因子会刺激血管生成。采用定量肠系膜窗分析法在大鼠中研究了内毒素(脂多糖,LPS)的血管生成作用。成年大鼠每天两次腹腔注射大肠杆菌LPS(5 pg/ml - 20,000 ng/ml),连续4.5天,在该治疗开始14天后处死。在浓度> 2 ng/ml时观察到血管生成反应呈剂量依赖性。在进行血管生成分析时,在测试组织中未见到炎性细胞渗出物。体重增加受抑制是LPS对大鼠全身作用的一个指标,仅在测试的最高剂量时显著。数据表明内毒素介导的新血管形成可能是炎症和伤口愈合的一个组成部分。