{"title":"Modeling pulmonary perfusion and gas exchange in alveolar microstructures","authors":"","doi":"10.1016/j.cma.2024.117499","DOIUrl":null,"url":null,"abstract":"<div><div>Pulmonary capillary perfusion and gas exchange are physiological processes that take place at the alveolar level and that are fundamental to sustaining life. Present-day computational simulations of these phenomena are based on low-dimensional mathematical models solved in idealized alveolar geometries, where the chemical reactions between O<span><math><msub><mrow></mrow><mrow><mn>2</mn></mrow></msub></math></span>-CO<span><math><msub><mrow></mrow><mrow><mn>2</mn></mrow></msub></math></span> and hemoglobin are simplified. While providing general insights, current modeling efforts fail to capture the complex chemical reactions that take place in pulmonary capillary blood flow on arbitrary geometries and ignore the crucial impact of microstructural morphology on pulmonary function. Here, we propose a coupled continuum perfusion and gas exchange model that captures complex gas and hemoglobin dynamics in realistic geometries of alveolar tissue. To this end, we derive appropriate governing equations incorporating a two-way Hill-like relationship between gas partial pressures and hemoglobin saturations. We numerically solve the resulting boundary-value problem using a non-linear finite-element approach to simulate and validate velocity, partial pressure, and hemoglobin saturation fields in simple geometries. We further perform sensitivity studies to understand the impact of blood speed and acidity variability on key physiological fields. Notably, we simulate perfusion and gas exchange on anatomical alveolar domains constructed from 3D <span><math><mi>μ</mi></math></span>-computed-tomography images of murine lungs. Based on these models, we show that morphological variations decrease O<span><math><msub><mrow></mrow><mrow><mn>2</mn></mrow></msub></math></span> and CO<span><math><msub><mrow></mrow><mrow><mn>2</mn></mrow></msub></math></span> diffusing capacity, predicting trends and values that are consistent with current medical knowledge. We envision that our model will provide an effective in silico framework to study how exercise and pathological conditions affect perfusion dynamics and the overall gas exchange function of the respiratory system. Source code is available at <span><span>https://github.com/comp-medicine-uc/alveolar-perfusion-transport-modeling</span><svg><path></path></svg></span>.</div></div>","PeriodicalId":55222,"journal":{"name":"Computer Methods in Applied Mechanics and Engineering","volume":null,"pages":null},"PeriodicalIF":6.9000,"publicationDate":"2024-11-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Computer Methods in Applied Mechanics and Engineering","FirstCategoryId":"5","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0045782524007539","RegionNum":1,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ENGINEERING, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
Abstract
Pulmonary capillary perfusion and gas exchange are physiological processes that take place at the alveolar level and that are fundamental to sustaining life. Present-day computational simulations of these phenomena are based on low-dimensional mathematical models solved in idealized alveolar geometries, where the chemical reactions between O-CO and hemoglobin are simplified. While providing general insights, current modeling efforts fail to capture the complex chemical reactions that take place in pulmonary capillary blood flow on arbitrary geometries and ignore the crucial impact of microstructural morphology on pulmonary function. Here, we propose a coupled continuum perfusion and gas exchange model that captures complex gas and hemoglobin dynamics in realistic geometries of alveolar tissue. To this end, we derive appropriate governing equations incorporating a two-way Hill-like relationship between gas partial pressures and hemoglobin saturations. We numerically solve the resulting boundary-value problem using a non-linear finite-element approach to simulate and validate velocity, partial pressure, and hemoglobin saturation fields in simple geometries. We further perform sensitivity studies to understand the impact of blood speed and acidity variability on key physiological fields. Notably, we simulate perfusion and gas exchange on anatomical alveolar domains constructed from 3D -computed-tomography images of murine lungs. Based on these models, we show that morphological variations decrease O and CO diffusing capacity, predicting trends and values that are consistent with current medical knowledge. We envision that our model will provide an effective in silico framework to study how exercise and pathological conditions affect perfusion dynamics and the overall gas exchange function of the respiratory system. Source code is available at https://github.com/comp-medicine-uc/alveolar-perfusion-transport-modeling.
期刊介绍:
Computer Methods in Applied Mechanics and Engineering stands as a cornerstone in the realm of computational science and engineering. With a history spanning over five decades, the journal has been a key platform for disseminating papers on advanced mathematical modeling and numerical solutions. Interdisciplinary in nature, these contributions encompass mechanics, mathematics, computer science, and various scientific disciplines. The journal welcomes a broad range of computational methods addressing the simulation, analysis, and design of complex physical problems, making it a vital resource for researchers in the field.