» Articles » PMID: 20507971

Modeling the Dynamics of Airway Constriction: Effects of Agonist Transport and Binding

Overview
Date 2010 May 29
PMID 20507971
Citations 14
Authors
Affiliations
Soon will be listed here.
Abstract

Recent advances have revealed that during exogenous airway challenge, airway diameters cannot be adequately predicted by their initial diameters. Furthermore, airway diameters can also vary greatly in time on scales shorter than a breath. To better understand these phenomena, we developed a multiscale model that allowed us to simulate aerosol challenge in the airways during ventilation. The model incorporates agonist-receptor binding kinetics to govern the temporal response of airway smooth muscle contraction on individual airway segments, which, together with airway wall mechanics, determines local airway caliber. Global agonist transport and deposition are coupled with pressure-driven flow, linking local airway constrictions with global flow dynamics. During the course of challenge, airway constriction alters the flow pattern, redistributing the agonist to less constricted regions. This results in a negative feedback that may be a protective property of the normal lung. As a consequence, repetitive challenge can cause spatial constriction patterns to evolve in time, resulting in a loss of predictability of airway diameters. Additionally, the model offers new insights into several phenomena including the intra- and interbreath dynamics of airway constriction throughout the tree structure.

Citing Articles

Oscillatory ventilation redux: alternative perspectives on ventilator-induced lung injury in the acute respiratory distress syndrome.

Kaczka D Curr Opin Physiol. 2021; 21:36-43.

PMID: 33898903 PMC: 8056876. DOI: 10.1016/j.cophys.2021.03.006.


Breath Hold Facilitates Targeted Deposition of Aerosolized Droplets in a 3D Printed Bifurcating Airway Tree.

Sonnenberg A, Taylor E, Mondonedo J, Bou Jawde S, Amin S, Song J Ann Biomed Eng. 2020; 49(2):812-821.

PMID: 32959135 PMC: 11470991. DOI: 10.1007/s10439-020-02623-9.


A review of inflammatory mechanism in airway diseases.

Aghasafari P, George U, Pidaparti R Inflamm Res. 2018; 68(1):59-74.

PMID: 30306206 DOI: 10.1007/s00011-018-1191-2.


Multiscale modeling methods in biomechanics.

Bhattacharya P, Viceconti M Wiley Interdiscip Rev Syst Biol Med. 2017; 9(3).

PMID: 28102563 PMC: 5412936. DOI: 10.1002/wsbm.1375.


Volatile Anesthetics and the Treatment of Severe Bronchospasm: A Concept of Targeted Delivery.

Mondonedo J, McNeil J, Amin S, Herrmann J, Simon B, Kaczka D Drug Discov Today Dis Models. 2016; 15:43-50.

PMID: 26744597 PMC: 4698912. DOI: 10.1016/j.ddmod.2014.02.004.


References
1.
Parameswaran H, Bartolak-Suki E, Hamakawa H, Majumdar A, Allen P, Suki B . Three-dimensional measurement of alveolar airspace volumes in normal and emphysematous lungs using micro-CT. J Appl Physiol (1985). 2009; 107(2):583-92. PMC: 2724324. DOI: 10.1152/japplphysiol.91227.2008. View

2.
Salerno F, Shinozuka N, Fredberg J, Ludwig M . Tidal volume amplitude affects the degree of induced bronchoconstriction in dogs. J Appl Physiol (1985). 1999; 87(5):1674-7. DOI: 10.1152/jappl.1999.87.5.1674. View

3.
Yang X, Liu Y, So R, Yang J . The effect of inlet velocity profile on the bifurcation COPD airway flow. Comput Biol Med. 2006; 36(2):181-94. DOI: 10.1016/j.compbiomed.2004.11.002. View

4.
Black L, Dellaca R, Jung K, Atileh H, Israel E, Ingenito E . Tracking variations in airway caliber by using total respiratory vs. airway resistance in healthy and asthmatic subjects. J Appl Physiol (1985). 2003; 95(2):511-8. DOI: 10.1152/japplphysiol.01114.2002. View

5.
Brusasco V, Pellegrino R . Complexity of factors modulating airway narrowing in vivo: relevance to assessment of airway hyperresponsiveness. J Appl Physiol (1985). 2003; 95(3):1305-13. DOI: 10.1152/japplphysiol.00001.2003. View