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Dynamic airway constriction in rats: heterogeneity and response to deep inspiration.大鼠动态气道收缩:异质性与深吸气反应。
Am J Physiol Lung Cell Mol Physiol. 2019 Jul 1;317(1):L39-L48. doi: 10.1152/ajplung.00050.2019. Epub 2019 Apr 24.
2
Assessment of airway response distribution and paradoxical airway dilation in mice during methacholine challenge.在乙酰甲胆碱激发试验期间对小鼠气道反应分布和矛盾性气道扩张的评估。
J Appl Physiol (1985). 2017 Mar 1;122(3):503-510. doi: 10.1152/japplphysiol.00476.2016. Epub 2016 Dec 29.
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Effects of repeated deep inspirations on recovery from methacholine-induced airway narrowing in normal subjects.重复深呼吸对正常受试者乙酰甲胆碱诱导的气道狭窄恢复的影响。
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本文引用的文献

1
Hyperresponsiveness: Relating the Intact Airway to the Whole Lung.高反应性:将完整气道与整个肺联系起来。
Physiology (Bethesda). 2017 Jul;32(4):322-331. doi: 10.1152/physiol.00008.2017.
2
Assessment of airway response distribution and paradoxical airway dilation in mice during methacholine challenge.在乙酰甲胆碱激发试验期间对小鼠气道反应分布和矛盾性气道扩张的评估。
J Appl Physiol (1985). 2017 Mar 1;122(3):503-510. doi: 10.1152/japplphysiol.00476.2016. Epub 2016 Dec 29.
3
Deep inspiration and the emergence of ventilation defects during bronchoconstriction: a computational study.深度吸气与支气管收缩期间通气缺陷的出现:一项计算研究
PLoS One. 2014 Nov 17;9(11):e112443. doi: 10.1371/journal.pone.0112443. eCollection 2014.
4
Smooth muscle in the maintenance of increased airway resistance elicited by methacholine in humans.平滑肌在人类乙酰甲胆碱引起的气道阻力增加中的维持作用。
Am J Respir Crit Care Med. 2014 Oct 15;190(8):879-85. doi: 10.1164/rccm.201403-0502OC.
5
What are ventilation defects in asthma?哮喘中的通气缺陷是什么?
Thorax. 2014 Jan;69(1):63-71. doi: 10.1136/thoraxjnl-2013-203711. Epub 2013 Aug 16.
6
Effects of lung inflation on airway heterogeneity during histaminergic bronchoconstriction.肺充气对组胺诱导支气管收缩时气道异质性的影响。
J Appl Physiol (1985). 2013 Sep 1;115(5):626-33. doi: 10.1152/japplphysiol.00476.2013. Epub 2013 Jun 27.
7
In situ casting and imaging of the rat airway tree for accurate 3D reconstruction.大鼠气道树的原位铸造与成像以实现精确的三维重建。
Exp Lung Res. 2013 Aug;39(6):249-57. doi: 10.3109/01902148.2013.801535. Epub 2013 Jun 20.
8
Production of Inhalable Submicrometer Aerosols from Conventional Mesh Nebulizers for Improved Respiratory Drug Delivery.通过传统网状雾化器生产可吸入亚微米气溶胶以改善呼吸道药物递送
J Aerosol Sci. 2012 Sep;51:66-80. doi: 10.1016/j.jaerosci.2012.04.002. Epub 2012 Apr 14.
9
Are all airways equal?所有气道都一样吗?
J Appl Physiol (1985). 2012 May;112(9):1431-2. doi: 10.1152/japplphysiol.00253.2012. Epub 2012 Mar 1.
10
Self-organized patterns of airway narrowing.气道狭窄的自组织模式。
J Appl Physiol (1985). 2011 May;110(5):1482-6. doi: 10.1152/japplphysiol.01163.2010. Epub 2011 Jan 20.

大鼠动态气道收缩:异质性与深吸气反应。

Dynamic airway constriction in rats: heterogeneity and response to deep inspiration.

机构信息

Department of Physiology, University of Tennessee Health Science Center , Memphis, Tennessee.

Department of Medicine, University of Tennessee Health Science Center , Memphis, Tennessee.

出版信息

Am J Physiol Lung Cell Mol Physiol. 2019 Jul 1;317(1):L39-L48. doi: 10.1152/ajplung.00050.2019. Epub 2019 Apr 24.

DOI:10.1152/ajplung.00050.2019
PMID:31017015
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6689744/
Abstract

Airway narrowing due to hyperresponsiveness severely limits gas exchange in patients with asthma. Imaging studies in humans and animals have shown that bronchoconstriction causes patchy patterns of ventilation defects throughout the lungs, and several computational models have predicted that these regions are due to constriction of smaller airways. However, these imaging approaches are often limited in their ability to capture dynamic changes in small airways, and the patterns of constriction are heterogeneous. To directly investigate regional variations in airway narrowing and the response to deep inspirations (DIs), we utilized tantalum dust and microfocal X-ray imaging of rat lungs to obtain dynamic images of airways in an intact animal model. Airway resistance was simultaneously measured using the flexiVent system. Custom-developed software was used to track changes in airway diameters up to (~0.3-3 mm). Changes in diameter during bronchoconstriction were then measured in response to methacholine (MCh) challenge. In contrast with the model predictions, we observed significantly greater percent constriction in larger airways in response to MCh challenge. Although there was a dose-dependent increase in total respiratory resistance with MCh, the percent change in airway diameters was similar for increasing doses. A single DI following MCh caused a significant reduction in resistance but did not cause a significant increase in airway diameters. Multiple DIs did, however, cause significant increases in airway diameters. These measurements allowed us to directly quantify dynamic changes in airways during bronchoconstriction and demonstrated greater constriction in larger airways.

摘要

气道高反应导致的气道狭窄严重限制了哮喘患者的气体交换。人体和动物的影像学研究表明,支气管收缩会导致肺部通气缺陷呈斑片状分布,并且几个计算模型预测这些区域是由于较小气道的收缩。然而,这些成像方法通常在捕捉小气道的动态变化方面能力有限,并且收缩模式具有异质性。为了直接研究气道狭窄的区域变化和对深吸气(DIs)的反应,我们利用钽尘和大鼠肺部的微焦点 X 射线成像,在完整的动物模型中获得气道的动态图像。同时使用 flexiVent 系统测量气道阻力。定制的软件用于跟踪气道直径的变化,最大可达 (~0.3-3 毫米)。然后测量在乙酰甲胆碱(MCh)挑战下支气管收缩时的直径变化。与模型预测相反,我们观察到在 MCh 挑战下,较大气道的收缩程度明显更大。尽管 MCh 会导致总呼吸阻力呈剂量依赖性增加,但气道直径的变化百分比对于增加的剂量是相似的。MCh 后进行单次 DI 会显著降低阻力,但不会显著增加气道直径。然而,多次 DI 确实会导致气道直径显著增加。这些测量允许我们直接量化支气管收缩期间气道的动态变化,并证明较大气道的收缩程度更大。