首页> 外文期刊>Burns: Including Thermal Injury >β-Glucan treatment prevents progressive burn ischaemia in the zone of stasis and improves burn healing: An experimental study in rats
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β-Glucan treatment prevents progressive burn ischaemia in the zone of stasis and improves burn healing: An experimental study in rats

机译:β-葡聚糖治疗可防止淤滞区域进行性烧伤缺血并改善烧伤愈合:一项在大鼠中的实验研究

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Saving the zone of stasis is one of the major goals of burn specialists. Increasing the tissue tolerance to ischaemia and inhibiting inflammation have been proposed to enable salvage of this zone. After a burn, excessive inflammation, including increased vascular permeability, local tissue oedema and neutrophil activation, causes local tissue damage by triggering vascular thrombosis and blocking capillaries, resulting in tissue ischaemia and necrosis. Oxygen radicals also contribute to tissue damage after a burn. However, macrophages play a pivotal role in the response to burn. We studied β-glucan because of its many positive systemic effects that are beneficial to burn healing, including immunomodulatory effects, antioxidant effects (free-radical scavenging activity) and effects associated with the reduction of the inflammatory response. There were four test groups in this study with eight rats in each group. Group 1 was the control group, group 2 was administered a local pomade (bacitracin + neomycin sulphate), group 3 received β-glucan (50 mg kg-1, orally) + the local pomade and group 4 received β-glucan. Burns were created using a brass comb model. Macroscopic, histopathological and statistical assessments were performed. Samples were harvested on the 3rd, 7th and 21 days for analysis. The neutrophilic infiltration into the zone of stasis was analysed on day 3. Macrophage infiltration, fibroblast proliferation, angiogenesis and re-epithelialisation ratios in the zone of stasis were analysed on days 7 and 21. The β-glucan groups (groups 3 and 4) exhibited lower neutrophil counts on the 3rd day, and macrophage infiltration, fibroblast proliferation, angiogenesis and re-epithelialisation were very high in these groups on the 7th day. In particular, re-epithelialisation on the 21st day was significantly better in the β-glucan groups. This study demonstrated that β-glucan may prevent neutrophil-dependent tissue damage and burn-induced oxidative injury through its anti-inflammatory and antioxidant properties. We speculate that the inhibition of neutrophil activation preserves vascular patency by preventing capillary blockage. β-Glucan is also a powerful macrophage stimulator, and is therefore very effective in saving the zone of stasis.
机译:保留停滞区是烧伤专家的主要目标之一。已经提出增加组织对局部缺血的耐受性并抑制炎症以使得能够挽救该区域。烧伤后,过度的炎症,包括增加的血管通透性,局部组织水肿和中性粒细胞活化,会通过触发血管血栓形成和阻塞毛细血管而引起局部组织损伤,从而导致组织缺血和坏死。烧伤后,氧自由基也有助于组织损伤。然而,巨噬细胞在烧伤反应中起关键作用。我们研究了β-葡聚糖,因为它具有许多有益于烧伤愈合的积极全身作用,包括免疫调节作用,抗氧化剂作用(自由基清除活性)以及与炎症反应减少相关的作用。本研究有四个测试组,每组八只大鼠。第一组为对照组,第二组给予局部润肤油(杆菌肽+新霉素硫酸盐),第3组接受β-葡聚糖(50 mg kg-1,口服)+局部润肤油,第4组接受β-葡聚糖。使用黄铜梳子模型创建烧伤。进行了宏观,组织病理学和统计学评估。在第3、7和21天收集样品进行分析。在第3天分析了中性粒细胞向淤积区的浸润。在第7天和第21天分析了淤积区中的巨噬细胞浸润,成纤维细胞增殖,血管生成和再上皮形成比例。β-葡聚糖组(第3和第4组)在第3天,这些患者的中性粒细胞计数较低,而在第7天,这些组的巨噬细胞浸润,成纤维细胞增殖,血管生成和上皮再形成非常高。特别是在第21天,β-葡聚糖组的再上皮化明显更好。这项研究表明,β-葡聚糖具有抗炎和抗氧化特性,可以预防中性粒细胞依赖性组织损伤和烧伤诱导的氧化损伤。我们推测中性粒细胞活化的抑制作用通过防止毛细血管阻塞来保持血管通畅。 β-葡聚糖也是强大的巨噬细胞刺激剂,因此在保存停滞区方面非常有效。

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