Pulmonary Oxygen Exchange in a Rhythmically Expanding–Contracting Alveolus–Capillary Model

Pulmonary gas exchanges are vital to human health, and disruptions to this process have been associated with many respiratory diseases. Previous gas exchange studies have predominately relied on whole-body testing and theoretical analysis with 1D or static models. However, pulmonary gas exchanges ar...

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Main Authors: Xiuhua April Si, Jinxiang Xi
Format: Article
Language:English
Published: MDPI AG 2022-11-01
Series:Journal of Respiration
Subjects:
Online Access:https://www.mdpi.com/2673-527X/2/4/15
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author Xiuhua April Si
Jinxiang Xi
author_facet Xiuhua April Si
Jinxiang Xi
author_sort Xiuhua April Si
collection DOAJ
description Pulmonary gas exchanges are vital to human health, and disruptions to this process have been associated with many respiratory diseases. Previous gas exchange studies have predominately relied on whole-body testing and theoretical analysis with 1D or static models. However, pulmonary gas exchanges are inherently a dynamic process in 3D spaces with instantaneous interactions between air, blood, and tissue. This study aimed to develop a computational model for oxygen exchange that considered all factors mentioned above. Therefore, an integrated alveolus–membrane–capillary geometry was developed with prescribed rhythmic expansion/contraction. Airflow ventilation, blood perfusion, and oxygen diffusion were simulated using COMSOL. The temporal and spatial distribution of blood flow and oxygen within the capillaries were simulated under varying breathing depths and cardiac outputs. The results showed highly nonuniform blood flow distributions in the capillary network, while the rhythmic oscillation further increased this nonuniformity, leading to stagnant blood flow in the distal vessels. A static alveolus–capillary geometry underestimated perfusion by 11% for normal respirations, and the deviation grew with breathing depth. The rhythmic motion caused a phase lag in the blood flow. The blood PO<sub>2</sub> reached equilibrium with the alveolar air after traveling 1/5–1/3 of the capillary network. The time to reach this equilibrium was significantly influenced by the air–blood barrier diffusivity, while it was only slightly affected by the perfusion rate. The computational platform in this study could be instrumental in obtaining refined knowledge of pulmonary O<sub>2</sub> exchanges.
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spelling doaj.art-ba4ca9932c8149778faf64913fd8ef6d2023-11-24T16:00:26ZengMDPI AGJournal of Respiration2673-527X2022-11-012415917310.3390/jor2040015Pulmonary Oxygen Exchange in a Rhythmically Expanding–Contracting Alveolus–Capillary ModelXiuhua April Si0Jinxiang Xi1Department of Aerospace, Industrial, and Mechanical Engineering, California Baptist University, Riverside, CA 92504, USADepartment of Biomedical Engineering, University of Massachusetts, Lowell, MA 01854, USAPulmonary gas exchanges are vital to human health, and disruptions to this process have been associated with many respiratory diseases. Previous gas exchange studies have predominately relied on whole-body testing and theoretical analysis with 1D or static models. However, pulmonary gas exchanges are inherently a dynamic process in 3D spaces with instantaneous interactions between air, blood, and tissue. This study aimed to develop a computational model for oxygen exchange that considered all factors mentioned above. Therefore, an integrated alveolus–membrane–capillary geometry was developed with prescribed rhythmic expansion/contraction. Airflow ventilation, blood perfusion, and oxygen diffusion were simulated using COMSOL. The temporal and spatial distribution of blood flow and oxygen within the capillaries were simulated under varying breathing depths and cardiac outputs. The results showed highly nonuniform blood flow distributions in the capillary network, while the rhythmic oscillation further increased this nonuniformity, leading to stagnant blood flow in the distal vessels. A static alveolus–capillary geometry underestimated perfusion by 11% for normal respirations, and the deviation grew with breathing depth. The rhythmic motion caused a phase lag in the blood flow. The blood PO<sub>2</sub> reached equilibrium with the alveolar air after traveling 1/5–1/3 of the capillary network. The time to reach this equilibrium was significantly influenced by the air–blood barrier diffusivity, while it was only slightly affected by the perfusion rate. The computational platform in this study could be instrumental in obtaining refined knowledge of pulmonary O<sub>2</sub> exchanges.https://www.mdpi.com/2673-527X/2/4/15gas exchangeoxygen partial pressurealveolus–capillarymicrovasculardiffusivityventilation–perfusion ratio
spellingShingle Xiuhua April Si
Jinxiang Xi
Pulmonary Oxygen Exchange in a Rhythmically Expanding–Contracting Alveolus–Capillary Model
Journal of Respiration
gas exchange
oxygen partial pressure
alveolus–capillary
microvascular
diffusivity
ventilation–perfusion ratio
title Pulmonary Oxygen Exchange in a Rhythmically Expanding–Contracting Alveolus–Capillary Model
title_full Pulmonary Oxygen Exchange in a Rhythmically Expanding–Contracting Alveolus–Capillary Model
title_fullStr Pulmonary Oxygen Exchange in a Rhythmically Expanding–Contracting Alveolus–Capillary Model
title_full_unstemmed Pulmonary Oxygen Exchange in a Rhythmically Expanding–Contracting Alveolus–Capillary Model
title_short Pulmonary Oxygen Exchange in a Rhythmically Expanding–Contracting Alveolus–Capillary Model
title_sort pulmonary oxygen exchange in a rhythmically expanding contracting alveolus capillary model
topic gas exchange
oxygen partial pressure
alveolus–capillary
microvascular
diffusivity
ventilation–perfusion ratio
url https://www.mdpi.com/2673-527X/2/4/15
work_keys_str_mv AT xiuhuaaprilsi pulmonaryoxygenexchangeinarhythmicallyexpandingcontractingalveoluscapillarymodel
AT jinxiangxi pulmonaryoxygenexchangeinarhythmicallyexpandingcontractingalveoluscapillarymodel