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早期诱导性急性肺损伤直接模型与间接模型的比较

Comparison of direct and indirect models of early induced acute lung injury.

作者信息

Chimenti Laura, Morales-Quinteros Luis, Puig Ferranda, Camprubi-Rimblas Marta, Guillamat-Prats Raquel, Gómez Maria Nieves, Tijero Jessica, Blanch Lluis, Matute-Bello Gustavo, Artigas Antonio

机构信息

Critical Care Centre, Parc Taulí Hospital Universitari, Institut d'Investigació i Innovació Parc Taulí I3PT, Universitat Autònoma de Barcelona, Parc Taulí 1, 08208, Sabadell, Spain.

Hospital Universitari Sagrat Cor., Grupo Quirón Salud, Barcelona, Spain.

出版信息

Intensive Care Med Exp. 2020 Dec 18;8(Suppl 1):62. doi: 10.1186/s40635-020-00350-y.

Abstract

BACKGROUND

The animal experimental counterpart of human acute respiratory distress syndrome (ARDS) is acute lung injury (ALI). Most models of ALI involve reproducing the clinical risk factors associated with human ARDS, such as sepsis or acid aspiration; however, none of these models fully replicates human ARDS.

AIM

To compare different experimental animal models of ALI, based on direct or indirect mechanisms of lung injury, to characterize a model which more closely could reproduce the acute phase of human ARDS.

MATERIALS AND METHODS

Adult male Sprague-Dawley rats were subjected to intratracheal instillations of (1) HCl to mimic aspiration of gastric contents; (2) lipopolysaccharide (LPS) to mimic bacterial infection; (3) HCl followed by LPS to mimic aspiration of gastric contents with bacterial superinfection; or (4) cecal ligation and puncture (CLP) to induce peritonitis and mimic sepsis. Rats were sacrificed 24 h after instillations or 24 h after CLP.

RESULTS

At 24 h, rats instilled with LPS or HCl-LPS had increased lung permeability, alveolar neutrophilic recruitment and inflammatory markers (GRO/KC, TNF-α, MCP-1, IL-1β, IL-6). Rats receiving only HCl or subjected to CLP had no evidence of lung injury.

CONCLUSIONS

Rat models of ALI induced directly by LPS or HCl-LPS more closely reproduced the acute phase of human ARDS than the CLP model of indirectly induced ALI.

摘要

背景

人类急性呼吸窘迫综合征(ARDS)的动物实验对应物是急性肺损伤(ALI)。大多数ALI模型涉及重现与人类ARDS相关的临床风险因素,如脓毒症或胃酸吸入;然而,这些模型均未完全复制人类ARDS。

目的

基于肺损伤的直接或间接机制,比较不同的ALI实验动物模型,以确定一种能更接近地复制人类ARDS急性期的模型。

材料与方法

成年雄性Sprague-Dawley大鼠接受气管内滴注:(1)盐酸以模拟胃内容物吸入;(2)脂多糖(LPS)以模拟细菌感染;(3)盐酸后接LPS以模拟胃内容物吸入合并细菌重叠感染;或(4)盲肠结扎和穿刺(CLP)以诱导腹膜炎并模拟脓毒症。滴注后24小时或CLP后24小时处死大鼠。

结果

24小时时,滴注LPS或盐酸-LPS的大鼠肺通透性增加、肺泡中性粒细胞募集及炎症标志物(GRO/KC、TNF-α、MCP-1、IL-1β、IL-6)升高。仅接受盐酸或进行CLP的大鼠无肺损伤证据。

结论

与间接诱导ALI的CLP模型相比,LPS或盐酸-LPS直接诱导的ALI大鼠模型更接近地复制了人类ARDS的急性期。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a2de/7746791/c318a85260da/40635_2020_350_Fig1_HTML.jpg

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