Phosphodiesterase-4 Inhibitor Roflumilast Attenuates Pulmonary Air Emboli-Induced Lung Injury

被引:12
|
作者
Peng, Chung-Kan [1 ]
Huang, Kun-Lun [1 ]
Wu, Chin-Pyng [2 ]
Wu, Yao-Kuang [3 ]
Tzeng, I-Shiang [4 ]
Lan, Chou-Chin [3 ]
机构
[1] Natl Def Med Ctr, Triserv Gen Hosp, Inst Undersea & Hyperbar Med, Div Pulm Med, Taipei, Taiwan
[2] Li Shin Hosp, Dept Crit Care Med, Taoyuan, Tao Yuan County, Taiwan
[3] Tzu Chi Univ, Buddhist Tzu Chi Med Fdn, Sch Med, Div Pulm Med,Taipei Tzu Chi Hosp, Hualien, Taiwan
[4] Buddhist Tzu Chi Med Fdn, Taipei Tzu Chi Hosp, Dept Res, New Taipei, Taiwan
关键词
Acute lung injury; Pulmonary air emboli; Phosphodiesterase-4; Roflumilast;
D O I
10.1016/j.jss.2019.03.028
中图分类号
R61 [外科手术学];
学科分类号
摘要
Background: Pulmonary air embolism (PAE)-induced acute lung injury (ALI) can be caused by massive air entry into the lung circulation. PAE can occur during diving, aviation, and some iatrogenic invasive procedures. PAE-induced ALI presents with severe inflammation, hypoxia, and pulmonary hypertension, and it is a serious complication resulting in significant morbidity and mortality. Phosphodiesterase-4 (PDE4) inhibitors can regulate inflammation and are therefore expected to have a therapeutic effect on ALI. However, the effect of the PDE4 inhibitor roflumilast on PAE-induced ALI is unknown. Methods: The PAE model was undertaken in isolated-perfused rat lungs. Four groups (n = 6 in each group) were defined as follows: control, PAE, PAE + roflumilast 2.5 mg/kg, and PAE + roflumilast 5 mg/kg. Induction of PAE-induced ALI was achieved via the infusion of 0.7 cc air through the pulmonary artery. Roflumilast was administered via perfusate. All groups were assessed for pulmonary microvascular permeability, lung histopathology changes, pulmonary edema (lung weight/body weight, lung wet/dry weight ratio), tumor necrosis factor alpha (TNF-alpha), interleukin-1 beta (IL-1 beta), IL-6, IL-17, nuclear factor-kappa B (NF-kappa B), and inhibitor of NF-kappa B alpha (I kappa B-alpha). Results: After the induction of air, PAE-induced ALI presented with pulmonary edema, pulmonary microvascular hyperpermeability, and lung inflammation with neutrophilic sequestration. The PAE-induced ALI also presented with increased expressions of IL-1 beta, IL-6, IL-8, IL-17, TNF-alpha, and NF-kappa B and decreased expression of I kappa B-alpha. The administration of roflumilast decreased pulmonary edema, inflammation, cytokines, NF-kappa B, and restored I kappa B-alpha level. Conclusions: PAE-induced ALI presents with lung inflammation with neutrophilic sequestration, pulmonary edema, hyperpermeability, increased cytokine levels, and activation of the NF-kappa B pathway. Roflumilast attenuates lung edema and inflammation and down-regulates the NF-kappa B pathway and cytokines. (C) 2019 Published by Elsevier Inc.
引用
收藏
页码:24 / 30
页数:7
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