Ecole polytechnique de Bruxelles, Transfers Interfaces and Processes, Université libre de Bruxelles , Brussels , Belgium.
Chest Department, Erasme University Hospital, Université libre de Bruxelles , Brussels , Belgium.
J Appl Physiol (1985). 2018 Apr 1;124(4):1025-1033. doi: 10.1152/japplphysiol.00530.2017. Epub 2018 Jan 11.
Although considered as an inflammation marker, exhaled nitric oxide (FNO) was shown to be sensitive to airway caliber changes to such an extent that it might be considered as a marker of them. It is thus important to understand how these changes and their localization mechanically affect the total NO flux penetrating the airway lumen ( JawNO), and hence FNO, independently from any inflammatory status change. In this work, a new model was used. It simulates NO production, consumption, and diffusion inside the airway epithelium, NO excretion from the epithelial wall into the airway lumen and, finally, its axial transport by diffusion and convection in the airway lumen. This model may also consider the possible presence of a fluid layer coating the epithelial wall. Simulations were performed. They show the great sensitivity of JawNO to peripheral airway caliber changes. Moreover, FNO shows distinct behaviors, depending on the location of the caliber change. Considering a bronchodilation, absence of FNO change was associated with dilation of central airways, FNO increase with dilation down to pre-acinar small airways, and FNO decrease with intra-acinar dilation due to the amplification of the back diffusion flux. The presence of a fluid layer was also shown to play a significant role in FNO changes. Altogether, the present work theoretically supports that specific FNO changes in acute situations are linked to specifically located airway caliber changes in the lung periphery. This opens the way for a new role for FNO as a functional marker of peripheral airway caliber change. NEW & NOTEWORTHY Using a new model of nitric oxide production and transport, allowing realistic simulation of airway caliber change, the present work theoretically supports that specific changes of the molar fraction of nitric oxide in the exhaled air, occurring without any change in the inflammatory status, are linked to specifically located airway caliber changes in the lung periphery. This opens the way for a new role for FNO as a functional marker of peripheral airway caliber change.
尽管呼气一氧化氮(FNO)被认为是一种炎症标志物,但它对气道口径变化非常敏感,以至于可以将其视为气道口径变化的标志物。因此,了解这些变化及其在机械上的定位如何影响穿透气道腔的总一氧化氮通量(JawNO),并因此独立于任何炎症状态变化来影响 FNO,这一点非常重要。在这项工作中,使用了一种新模型。它模拟了气道上皮内一氧化氮的产生、消耗和扩散、上皮壁内一氧化氮排泄到气道腔、以及最终通过气道腔中的扩散和对流进行轴向运输。该模型还可以考虑可能存在覆盖上皮壁的液层。进行了模拟。结果表明,JawNO 对周围气道口径变化非常敏感。此外,FNO 的行为也不同,这取决于口径变化的位置。考虑到支气管扩张,FNO 没有变化与中央气道扩张有关,FNO 增加与扩张到前腺小气道有关,FNO 减少与腺内扩张有关,这是由于后扩散通量的放大。还表明存在液层也会对 FNO 变化产生重大影响。总的来说,这项工作从理论上支持了在急性情况下,特定的 FNO 变化与肺部外周特定位置的气道口径变化有关。这为 FNO 作为外周气道口径变化的功能标志物开辟了新的途径。