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啮齿动物中脂多糖诱导的肺损伤的分子动力学

Molecular Dynamics of Lipopolysaccharide-Induced Lung Injury in Rodents.

作者信息

Domscheit Hannes, Hegeman Maria A, Carvalho Niedja, Spieth Peter M

机构信息

Department of Anesthesiology and Critical Care Medicine, University Hospital Dresden, Technische Universität Dresden, Dresden, Germany.

Laboratory of Experimental Intensive Care and Anesthesiology (L∙E∙I∙C∙A), Department of Intensive Care, Academic Medical Center, Amsterdam, Netherlands.

出版信息

Front Physiol. 2020 Feb 5;11:36. doi: 10.3389/fphys.2020.00036. eCollection 2020.

Abstract

Acute respiratory distress syndrome (ARDS) is a common disease entity in critical care medicine and is still associated with a high mortality. Because of the heterogeneous character of ARDS, animal models are an insturment to study pathology in relatively standardized conditions. Rodent models can bridge the gap from investigations to large animal and clinical trials by facilitating large sample sizes under physiological conditions at comparatively low costs. One of the most commonly used rodent models of acute lung inflammation and ARDS is administration of lipopolysaccharide (LPS), either into the airways (direct, pulmonary insult) or systemically (indirect, extra-pulmonary insult). This narrative review discusses the dynamics of important pathophysiological pathways contributing to the physiological response to LPS-induced injury. Pathophysiological pathways of LPS-induced lung injury are not only influenced by the type of the primary insult (e.g., pulmonary or extra-pulmonary) and presence of additional stimuli (e.g., mechanical ventilation), but also by time. As such, findings in animal models of LPS-induced lung injury may depend on the time point at which samples are obtained and physiological data are captured. This review summarizes the current evidence and highlights uncertainties on the molecular dynamics of LPS-induced lung injury in rodent models, encouraging researchers to take accurate timing of LPS-induced injury into account when designing experimental trials.

摘要

急性呼吸窘迫综合征(ARDS)是重症医学中的一种常见病症,其死亡率仍然很高。由于ARDS具有异质性,动物模型是在相对标准化条件下研究病理的一种工具。啮齿动物模型可以通过在生理条件下以相对较低的成本实现大样本量,从而弥合从研究到大型动物和临床试验之间的差距。急性肺部炎症和ARDS最常用的啮齿动物模型之一是将脂多糖(LPS)经气道给药(直接,肺部损伤)或全身给药(间接,肺外损伤)。这篇叙述性综述讨论了导致对LPS诱导损伤产生生理反应的重要病理生理途径的动态变化。LPS诱导的肺损伤的病理生理途径不仅受原发性损伤类型(例如,肺部或肺外)和其他刺激因素(例如,机械通气)的影响,还受时间的影响。因此,LPS诱导的肺损伤动物模型中的研究结果可能取决于获取样本和记录生理数据的时间点。本综述总结了当前证据,并强调了啮齿动物模型中LPS诱导的肺损伤分子动态方面的不确定性,鼓励研究人员在设计实验时考虑LPS诱导损伤的准确时间。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bf0a/7012903/6b098500ef1f/fphys-11-00036-g001.jpg

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