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捕捉急性呼吸窘迫综合征的多因素本质——模拟小鼠急性肺损伤的“两次打击”方法。

Capturing the multifactorial nature of ARDS - "Two-hit" approach to model murine acute lung injury.

作者信息

Hoegl Sandra, Burns Nana, Angulo Martín, Francis Daniel, Osborne Christopher M, Mills Tingting W, Blackburn Michael R, Eltzschig Holger K, Vohwinkel Christine U

机构信息

Organ Protection Program, School of Medicine, Department of Anesthesiology, University of Colorado, Aurora, Colorado.

Developmental Lung Biology, Cardio Vascular Pulmonary Research Laboratories, Division of Pulmonary Sciences and Critical Care Medicine, Division of Pediatric Critical Care, Departments of Medicine and Pediatrics, University of Colorado, Anschutz Medical Campus, Aurora, Colorado.

出版信息

Physiol Rep. 2018 Mar;6(6):e13648. doi: 10.14814/phy2.13648.

Abstract

Severe acute respiratory distress syndrome (ARDS) presents typically with an initializing event, followed by the need for mechanical ventilation. Most animal models of ALI are limited by the fact that they focus on a singular cause of acute lung injury (ALI) and therefore fail to mimic the complex, multifactorial pathobiology of ARDS. To better capture this scenario, we provide a comprehensive characterization of models of ALI combining two injuries: intra tracheal (i.t.) instillation of LPS or hypochloric acid (HCl) followed by ventilator-induced lung injury (VILI). We hypothesized, that mice pretreated with LPS or HCl prior to VILI and thus receiving a ("two-hit injury") will sustain a superadditive lung injury when compared to VILI. Mice were allocated to following treatment groups: control with i.t. NaCl, ventilation with low peak inspiratory pressure (PIP), i.t. HCl, i.t. LPS, VILI (high PIP), HCl i.t. followed by VILI and LPS i.t. followed by VILI. Severity of injury was determined by protein content and MPO activity in bronchoalveolar lavage (BAL), the expression of inflammatory cytokines and histopathology. Mice subjected to VILI after HCl or LPS instillation displayed augmented lung injury, compared to singular lung injury. However, mice that received i.t. LPS prior to VILI showed significantly increased inflammatory lung injury compared to animals that underwent i.t. HCl followed by VILI. The two-hit lung injury models described, resulting in additive but differential acute lung injury recaptures the clinical relevant multifactorial etiology of ALI and could be a valuable tool in translational research.

摘要

重症急性呼吸窘迫综合征(ARDS)通常表现为有一个起始事件,随后需要机械通气。大多数急性肺损伤(ALI)动物模型的局限性在于它们聚焦于急性肺损伤的单一病因,因此无法模拟ARDS复杂的多因素病理生物学过程。为了更好地呈现这种情况,我们对结合两种损伤的ALI模型进行了全面表征:气管内(i.t.)注入脂多糖(LPS)或次氯酸(HCl),随后进行呼吸机诱导的肺损伤(VILI)。我们假设,在VILI之前用LPS或HCl预处理从而接受“两次打击损伤”的小鼠,与单纯VILI相比,将遭受超相加性肺损伤。将小鼠分配到以下治疗组:气管内注入生理盐水的对照组、低吸气峰压(PIP)通气组、气管内注入HCl组、气管内注入LPS组、VILI(高PIP)组、气管内注入HCl后进行VILI组以及气管内注入LPS后进行VILI组。通过支气管肺泡灌洗(BAL)中的蛋白含量和髓过氧化物酶(MPO)活性、炎性细胞因子的表达以及组织病理学来确定损伤的严重程度。与单一肺损伤相比,在注入HCl或LPS后遭受VILI的小鼠表现出加重的肺损伤。然而,与先进行气管内注入HCl随后进行VILI的动物相比,在VILI之前接受气管内注入LPS的小鼠表现出明显加重的炎性肺损伤。所描述的两次打击肺损伤模型导致相加但有差异的急性肺损伤,重现了ALI临床相关的多因素病因,并且可能是转化研究中的一个有价值的工具。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8245/5875538/f7b5d81abb34/PHY2-6-e13648-g001.jpg

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