Pathogenesis of ventilator-induced lung injury: metabolomics analysis of the lung and plasma.

Yanfei Mao, Zhixin Ma, Chufan Xu, Zhou Lv, Wenwen Dong, Xinru Liu
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Abstract

Introduction: Nowadays,the mechanical ventilation (MV) aims to rest the respiratory muscles while providing adequate gas exchange, and it has been a part of basic life support during general anesthesia as well as in critically ill patients with and without respiratory failure. However, MV itself has the potential to cause or worsen lung injury, which is also known as ventilator-induced lung injury (VILI). Thus, the early diagnosis of VILI is of great importance for the prevention and treatment of VILI.

Objective: This study aimed to investigate the metabolomes in the lung and plasma of mice receiving mechanical ventilation (MV).

Methods: Healthy mice were randomly assigned into control group; (2) high volume tidal (HV) group (30 ml/kg); (3) low volume tidal (LV) group (6 ml/kg). After ventilation for 4 h, mice were sacrificed and the lung tissue and plasma were collected. The lung and plasma were processed for the metabolomics analysis. We also performed histopathological examination on the lung tissue.

Results: We detected moderate inflammatory damage with alveolar septal thickening in the HV group compared with the normal and LV groups.The metabolomics analysis results showed MV altered the metabolism which was characterized by the dysregulation of γ-amino butyric acid (GABA) system and urea cycle (desregulations in plasma and lung guanidinosuccinic acid, argininosuccinic acid, succinic acid semialdehyde and lung GABA ), Disturbance of citric acid cycle (CAC) (increased plasma glutamine and lung phosphoenol pyruvate) and redox imbalance (desregulations in plasma and/or lung ascorbic acid, chenodeoxycholic acid, uric acid, oleic acid, stearidonic acid, palmitoleic acid and docosahexaenoic acid). Moreover, the lung and plasma metabolomes were also significantly different between LV and HV groups.

Conclusions: Some lung and plasma metabolites related to the GABA system and urea cycle, citric acid cycle and redox balance were significantly altered, and they may be employed for the evaluation of VILI and serve as targets in the treatment of VILI.

呼吸机所致肺损伤的发病机制:肺和血浆代谢组学分析。
目前,机械通气(MV)的目的是在保证呼吸肌休息的同时提供足够的气体交换,已成为全身麻醉以及有或无呼吸衰竭的危重患者基本生命支持的一部分。然而,MV本身有可能引起或加重肺损伤,也称为呼吸机诱导肺损伤(VILI)。因此,VILI的早期诊断对于VILI的预防和治疗具有重要意义。目的:研究机械通气小鼠肺及血浆代谢组的变化。方法:将健康小鼠随机分为对照组;(2)高容量潮汐(HV)组(30 ml/kg);(3)低容量潮汐(LV)组(6ml /kg)。通气4 h后处死小鼠,收集肺组织和血浆。对肺和血浆进行代谢组学分析。我们还对肺组织进行了组织病理学检查。结果:与正常组和LV组比较,HV组可见中度炎症损伤,肺泡间隔增厚。代谢组学分析结果显示,MV改变了小鼠的代谢,其特征是γ-氨基丁酸(GABA)系统和尿素循环失调(血浆和肺中胍丁二酸、精氨酸丁二酸、丁二酸半醛和肺中GABA),柠檬酸循环失调(血浆中谷氨酰胺和肺中磷酸烯醇丙酮酸升高)和氧化还原失衡(血浆和/或肺中抗坏血酸、鹅去氧胆酸、尿酸、油酸、硬脂酸、棕榈油酸和二十二碳六烯酸)。此外,肺和血浆代谢组在LV和HV组之间也有显著差异。结论:一些与GABA系统、尿素循环、柠檬酸循环及氧化还原平衡相关的肺和血浆代谢物明显改变,这些代谢物可用于VILI的评估,并可作为治疗VILI的靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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