人体运动时肺毛细血管血容量和弥散膜容量:肺动脉压的作用。

IF 3.5 2区 医学 Q1 PHYSIOLOGY
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

摘要

运动时,肺一氧化碳弥散能力(DLCO)、肺毛细血管血容量(Vc)和弥散膜容量(DM)增加,继发于肺动脉压(PAP)和中央血容量动员的升高。虽然中心血容量对DLCO的作用已经确定,但PAP对运动期间DLCO、Vc和DM的影响尚不清楚。基于先前的工作,我们验证了PAP急性增加会通过DM增加来增强运动DLCO的假设。15名健康年轻人(7名女性;年龄:24±4岁)在60W时完成两组自行车运动,(CUFF)或(CON)双侧大腿袖充气加压至90mmhg。采用吸入O2-DLCO的多重分数法测定两种运动条件下的DLCO、Vc和DM以及心输出量(Q³c;阻抗心电图)和右心室收缩压(RVSP;超声心动图)。CUFF运动导致RVSP增加更大(CUFF: 44.7±6.1 vs. CON: 38.9±5.5 mmHg;P=0.036),但与CON相比,Q (c) (P=0.644)或V (O2) (P=0.976)没有变化。CUFF运动时DLCO较高(CUFF: 41±6 vs CON: 38±6 ml/min/mmHg;P=0.001),并且由DM增加介导(CUFF: 138±55 vs. CON: 90±39 ml/min/mmHg;P=0.032),非Vc (CUFF: 85±18 vs. CON: 98±27 ml/min/mmHg;P = 0.820)。RVSP升高与DM呈正相关(rrm=0.82;P=0.024),但与Vc呈负相关(rrm=-0.80, P=0.029)。总的来说,这些数据表明PAP在低强度运动期间主要通过增加毛细血管募集(即DM)来促进DLCO。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Pulmonary capillary blood volume and diffusing membrane capacity during exercise in humans: role of pulmonary artery pressure.

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. Although 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 yr) completed two bouts of cycling exercise at 60 W, with (CUFF) or without (CON) bilateral thigh cuff inflation pressurized to 90 mmHg. The multiple fractions of the inspired O2-DLCO method were 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 with CON. DLCO was higher during the 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 to DM (rrm = 0.82; P = 0.024) but inversely related to 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).NEW & NOTEWORTHY Pulmonary artery pressure contributes to DLCO recruitment during exercise. However, it is unclear how pulmonary artery pressure impacts the pulmonary microcirculatory adjustments that comprise DLCO, namely Vc and DM. Using subsystolic occlusion of the locomotor muscles during exercise to induce increases in pulmonary artery pressure, without changes in cardiac output or metabolic demand, we demonstrate that pulmonary artery pressure contributes to DLCO during exercise via heightened capillary recruitment (DM).

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来源期刊
CiteScore
9.20
自引率
4.10%
发文量
146
审稿时长
2 months
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.
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