Department of Burns, The First Affiliated Hospital of Nanchang University, Nanchang, Jiangxi 330006, P.R. China.
Department of Pathology, The First Affiliated Hospital of Nanchang University, Nanchang, Jiangxi 330006, P.R. China.
Mol Med Rep. 2017 Nov;16(5):7375-7381. doi: 10.3892/mmr.2017.7537. Epub 2017 Sep 20.
The aim of the present study was to determine the effects of early anticoagulation treatment on severe burns complicated by inhalation injury in a rabbit model. Under anesthetization, an electrical burns instrument (100˚C) was used to scald the backs of rabbits for 15 sec, which established a 30% III severe burns model. Treatment of the rabbits with early anticoagulation effectively improved the severe burns complicated by inhalation injury‑induced lung injury, reduced PaO2, PaCO2 and SPO2 levels, suppressed the expression of tumor necrosis factor‑α, interleukin (IL)‑1β and IL‑6, and increased the activity of IL‑10. In addition, it was found that early anticoagulation treatment effectively suppressed the activities of caspase‑3 and caspase‑9, upregulated the protein expression of vascular endothelial growth factor (VEGF) and decreased the protein expression of protease‑activated receptor 1 (PAR1) in the severe burns model. It was concluded that early anticoagulation treatment affected the severe burns complicated by inhalation injury in a rabbit model through the upregulation of VEGF and downregulation of PAR1 signaling pathways. Thus, early anticoagulation is a potential therapeutic option for severe burns complicated by inhalation injury.
本研究旨在确定早期抗凝治疗对兔严重烧伤合并吸入性损伤模型的影响。在麻醉下,使用电烧伤仪(100°C)将兔子的背部烫伤 15 秒,建立 30%III 度严重烧伤模型。早期抗凝治疗可有效改善严重烧伤合并吸入性损伤引起的肺损伤,降低 PaO2、PaCO2 和 SPO2 水平,抑制肿瘤坏死因子-α、白细胞介素(IL)-1β 和 IL-6 的表达,增加 IL-10 的活性。此外,研究还发现,早期抗凝治疗可有效抑制 caspase-3 和 caspase-9 的活性,上调血管内皮生长因子(VEGF)的蛋白表达,降低蛋白酶激活受体 1(PAR1)的蛋白表达。结论:早期抗凝治疗通过上调 VEGF 和下调 PAR1 信号通路影响兔严重烧伤合并吸入性损伤模型。因此,早期抗凝治疗是严重烧伤合并吸入性损伤的一种潜在治疗选择。