Andrew W D'Souza, Andrew R Brotto, Bronwen Hicks, Eli Bok, Jason Weatherald, Sean Van Diepen, Michael K Stickland
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引用次数: 0
Abstract
During exercise, lung diffusing capacity for carbon monoxide (DLCO), pulmonary capillary blood volume (Vc), and diffusing membrane capacity (DM) increase secondary to a rise in pulmonary artery pressure (PAP) and central blood volume mobilization. While the role of central blood volume on DLCO is well established, the impact of PAP on DLCO, Vc, and DM during exercise is less clear. Based on previous work, we tested the hypothesis that acute increases in PAP will potentiate exercise DLCO via increases in DM. Fifteen healthy young adults (7 females; age: 24±4 years) completed two bouts of cycling exercise at 60W, with (CUFF) or without (CON) bilateral thigh cuff inflation pressurized to 90 mmHg. The multiple fractions of inspired O2-DLCO method was used to determine DLCO, Vc and DM at baseline and during both exercise conditions alongside estimates of cardiac output (Q̇c; impedance cardiography), and right ventricular systolic pressure (RVSP; echocardiography). CUFF exercise resulted in a larger increase in RVSP (CUFF: 44.7±6.1 vs. CON: 38.9±5.5 mmHg; P=0.036), but not Q̇c (P=0.644) or V̇O2 (P=0.976) compared to CON. DLCO was higher during CUFF exercise (CUFF: 41±6 vs. CON: 38±6 ml/min/mmHg; P=0.001), and was mediated by increases in DM (CUFF: 138±55 vs. CON: 90±39 ml/min/mmHg; P=0.032), not Vc (CUFF: 85±18 vs. CON: 98±27 ml/min/mmHg; P=0.820). Increases in RVSP were positively related with DM (rrm=0.82; P=0.024) but inversely related with Vc (rrm=-0.80, P=0.029). Collectively, these data indicate that PAP primarily contributes to DLCO during low intensity exercise via increases in capillary recruitment (i.e., DM).
期刊介绍:
The American Journal of Physiology-Lung Cellular and Molecular Physiology publishes original research covering the broad scope of molecular, cellular, and integrative aspects of normal and abnormal function of cells and components of the respiratory system. Areas of interest include conducting airways, pulmonary circulation, lung endothelial and epithelial cells, the pleura, neuroendocrine and immunologic cells in the lung, neural cells involved in control of breathing, and cells of the diaphragm and thoracic muscles. The processes to be covered in the Journal include gas-exchange, metabolic control at the cellular level, intracellular signaling, gene expression, genomics, macromolecules and their turnover, cell-cell and cell-matrix interactions, cell motility, secretory mechanisms, membrane function, surfactant, matrix components, mucus and lining materials, lung defenses, macrophage function, transport of salt, water and protein, development and differentiation of the respiratory system, and response to the environment.