Unsteady diffusional screening in 3D pulmonary acinar structures: from infancy to adulthood. Issue 11 (26th July 2016)

• Record Type: Journal Article
• Authors: Hofemeier, Philipp; Shachar-Berman, Lihi; Tenenbaum-Katan, Janna; Filoche, Marcel; Sznitman, Josué
• Is Part Of: Journal of biomechanics. Volume 49:Issue 11(2016)
• Page Start: 2193
• Page End: 2200
• Publication Date: 2016-07-26
• Subjects: Diffusional screening -- Pulmonary flows -- Oxygen transport -- Developing acini; Animal mechanics -- Periodicals; Biomechanics -- Periodicals; Biomechanics -- Periodicals; Mécanique animale -- Périodiques; Biomécanique -- Périodiques; Electronic journals; 571.4305
• DOI: 10.1016/j.jbiomech.2015.11.039
• Languages: English
• ISSNs: 0021-9290

Abstract

Abstract: Diffusional screening in the lungs is a physical phenomenon where the specific topological arrangement of alveolated airways of the respiratory region leads to a depletion, or 'screening', of oxygen molecules with increasing acinar generation. Here, we revisit diffusional screening phenomena in anatomically-inspired pulmonary acinar models under realistic breathing maneuvers. By modelling 3D bifurcating alveolated airways capturing both convection and diffusion, unsteady oxygen transport is investigated under cyclic breathing motion. To evaluate screening characteristics in the developing lungs during growth, four representative stages of lung development were chosen (i.e. 3 months, 1 year and 9 months, 3 years and adulthood) that capture distinct morphological acinar changes spanning alveolarization phases to isotropic alveolar growth. Numerical simulations unveil the dramatic changes in O2 transport occurring during lung development, where young infants exhibit highest acinar efficiencies that rapidly converge with age to predictions at adulthood. With increased ventilatory effort, transient dynamics of oxygen transport is fundamentally altered compared to tidal breathing and emphasizes the augmented role of convection. Resolving the complex convective acinar flow patterns in 3D acinar trees allows for the first time a spatially-localized and time-resolved characterization of oxygen transport in the pulmonary acinus, from infancy to adulthood.