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Early anticoagulation therapy for severe burns complicated by inhalation injury in a rabbit model

机译:早期抗凝治疗严重烧伤并吸入损伤的兔模型

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摘要

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.
机译:本研究的目的是确定早期抗凝治疗对严重烧伤并吸入损伤的兔模型的影响。在麻醉下,使用电灼伤仪(100°C)将兔子的背部烫伤15秒钟,建立了30%III严重灼伤模型。早期抗凝治疗兔可有效改善严重烧伤并发吸入性肺损伤,降低PaO2,PaCO2和SPO2水平,抑制肿瘤坏死因子-α,白介素(IL)-1β和IL-6的表达,并增加了IL-10的活性。此外,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,并降低蛋白酶激活受体1(PAR1)的蛋白表达。严重烧伤模型。结论是,早期抗凝治疗可通过上调VEGF和下调PAR1信号通路来影响兔子模型中的严重烧伤,并伴有吸入性损伤。因此,早期的抗凝治疗是严重烧伤并吸入损伤的潜在治疗选择。

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