Department of Anaesthesiology, Medical Centre of the Johannes Gutenberg University, Mainz, Germany.
Department of Anaesthesiology, Medical Centre of the Johannes Gutenberg University, Mainz, Germany.
Vet Anaesth Analg. 2021 Jan;48(1):26-34. doi: 10.1016/j.vaa.2020.08.008. Epub 2020 Oct 21.
To establish and evaluate a standardized method of targeted, intrabronchial drug delivery in pigs.
Randomized controlled trial.
A total of 16 German Landrace pigs (Sus scrofa), age range 12‒16 weeks, and weighing 28‒35 kg.
The animals were anaesthetized, intubated, and instrumented with extended cardiovascular monitoring. Lung injury was induced by administering via a flexible fibre-optic endoscope using 100 mL saline solution containing either 20 mg of Escherichia coli lipopolysaccharide (E. coli LPS) (n = 8) or no additive (sham, n = 8) into the two distal mainstem bronchi. The animals were monitored for 8 hours and arterial oxygenation, inspiratory pressure and arterial blood pressure were measured repeatedly. Post-mortem, lung tissue was prepared for histologic damage scoring and determination of proinflammatory cytokines Interleukin-6 (IL-6) and tumour necrosis factor alpha (TNFα). Statistical analyses were performed using inter-group analysis of variance and Student's t tests. Data are presented as mean ± standard deviation. A p value <0.05 was considered significant.
The targeted application of LPS led to significant deterioration of oxygenation consistent with mild-to-moderate acute respiratory distress syndrome (ARDS) and hypotension (Horowitz ratio: sham 2 hour, 300 ± 39; LPS 2 hour, 193.7 ± 52; p < 0.001). Histologic analyses identified increased inflammation and oedema in the tissues of the animals in the LPS group IL-6 sham: 6.4 ± 4.4 × 10 pg mL; IL-6 LPS: 2.8 ± 2.4 × 10 pg mL, p = 0.015.
The targeted application of agents via flexible fibre-optic endoscopy is a valid, reliable method of causing controlled lung damage in a porcine model. The data presented suggest the feasibility and possible advantages of controlled application and could expand the array of techniques used to help understand the critical condition of ARDS. In addition, a targeted approach could help reduce animal numbers used for this purpose.
建立并评估一种针对猪支气管内靶向药物输送的标准化方法。
随机对照试验。
共 16 头德国长白猪(Sus scrofa),年龄 12-16 周,体重 28-35kg。
动物麻醉、插管并进行扩展心血管监测。通过柔性纤维内镜将 100ml 生理盐水(含有 20mg 大肠杆菌脂多糖(E. coli LPS))或无添加剂(假手术,n=8)注入两个远端主支气管,诱发肺损伤。动物监测 8 小时,反复测量动脉氧合、吸气压力和动脉血压。死后,准备肺组织进行组织学损伤评分和促炎细胞因子白细胞介素-6(IL-6)和肿瘤坏死因子-α(TNFα)的测定。使用组间方差分析和学生 t 检验进行统计学分析。数据表示为均数±标准差。p 值<0.05 认为有统计学意义。
LPS 的靶向应用导致氧合明显恶化,符合轻度至中度急性呼吸窘迫综合征(ARDS)和低血压(Horowitz 比:假手术 2 小时,300±39;LPS 2 小时,193.7±52;p<0.001)。组织学分析发现 LPS 组动物组织中炎症和水肿增加 IL-6 假手术:6.4±4.4×10pg/ml;IL-6 LPS:2.8±2.4×10pg/ml,p=0.015。
通过柔性纤维内镜靶向应用药物是一种在猪模型中引起可控性肺损伤的有效、可靠方法。所提供的数据表明了该方法的可行性和潜在优势,并可能扩展用于帮助理解 ARDS 危急情况的技术手段。此外,靶向方法可以帮助减少为此目的使用的动物数量。