Resistive breathing aggravates cigarette smoke-induced pulmonary inflammation.

IF 4 3区 医学 Q1 RESPIRATORY SYSTEM
ERJ Open Research Pub Date : 2025-08-26 eCollection Date: 2025-07-01 DOI:10.1183/23120541.00974-2024
Eleftheria Mizi, Vyronia Vassilakopoulou, Athanasia Chatzianastasiou, Theocharis Georgiadis, Constantinos Glynos, Stamatios Theocharis, Theodoros Vassilakopoulos, Dimitrios Toumpanakis
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引用次数: 0

Abstract

Introduction: Resistive breathing (RB) is the hallmark of diseases of airway obstruction, especially during exacerbations, resulting in significant mechanical stress on the lung. RB induces pulmonary inflammation and injury in previously healthy animals. Whether RB exerts additional injurious effects when superimposed on cigarette smoke (CS) exposure is unknown.

Methods: Adult mice were exposed to CS for 1 or 6 months, followed by RB for 24 h, induced through tracheal banding. Subsequently, respiratory system mechanics were assessed, bronchoalveolar lavage (BAL) was performed and cytokine levels were measured by ELISA in lung tissue samples. Surfactant protein D (SP-D) was measured in blood, and BAL and histology were performed. Emphysema was quantified by the mean linear intercept (Lm) and the destructive index (DI).

Results: CS exposure for 1 and 6 months increased BAL cellularity (∼8-fold and ∼1.9-fold to air, respectively, p<0.01). RB aggravated BAL cellularity at both time points (p=0.025 and p=0.002 to CS) and increased MCP-1 levels at 1 month (p=0.002 to control). Histology revealed augmented focal membrane thickening at 1 month following combination of RB with CS exposure (p=0.011), while at 6 months emphysema was more severe after RB in CS-exposed mice (p=0.001 to CS for both Lm and DI). CS increased Sp-D levels in BAL (p<0.01 at both time points), while RB caused increased levels in blood (p<0.01 to CS). RB decreased static compliance at 1 month of air exposure (p=0.007).

Conclusion: Combining resistive breathing with cigarette smoke exposure results in augmented inflammatory responses, increased lung injury and augmented emphysema.

Abstract Image

Abstract Image

Abstract Image

呼吸困难会加重香烟引起的肺部炎症。
导读:呼吸阻力(RB)是气道梗阻疾病的标志,特别是在加重期间,导致肺受到显著的机械应力。RB在先前健康的动物中诱导肺部炎症和损伤。当与香烟烟雾(CS)接触时,RB是否会产生额外的伤害效应尚不清楚。方法:成年小鼠分别暴露于CS 1、6个月后,再经气管束带诱导给予RB 24 h。随后,评估呼吸系统力学,进行支气管肺泡灌洗(BAL),并通过ELISA检测肺组织样本的细胞因子水平。测定血中表面活性蛋白D (SP-D),并进行BAL和组织学检查。用平均线性截距(Lm)和破坏指数(DI)对肺气肿进行量化。结果:暴露于CS 1个月和6个月后,BAL细胞数量分别增加了8倍和1.9倍。结论:抵抗性呼吸与香烟烟雾暴露相结合会导致炎症反应增强,肺损伤增加和肺气肿增加。
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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来源期刊
ERJ Open Research
ERJ Open Research Medicine-Pulmonary and Respiratory Medicine
CiteScore
6.20
自引率
4.30%
发文量
273
审稿时长
8 weeks
期刊介绍: ERJ Open Research is a fully open access original research journal, published online by the European Respiratory Society. The journal aims to publish high-quality work in all fields of respiratory science and medicine, covering basic science, clinical translational science and clinical medicine. The journal was created to help fulfil the ERS objective to disseminate scientific and educational material to its members and to the medical community, but also to provide researchers with an affordable open access specialty journal in which to publish their work.
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