期刊
JOURNAL OF PHYSIOLOGY-LONDON
卷 598, 期 3, 页码 599-610出版社
WILEY
DOI: 10.1113/JP279135
关键词
blood flow; lung disease; O-2 uptake; O-2 delivery
资金
- National Heart, Lung, and Blood Institute [HL-091830]
- Ruth L. Kirschstein National Research Service Award [1T32HL139451]
- Veterans Administration Rehabilitation Research and Development Service [E6910-R, E1697-R, E1433-P, E9275-L, E1572-P]
Key points Peak oxygen uptake, a primary determinant of prognosis, mortality and quality of life, is diminished in patients with chronic obstructive pulmonary disease (COPD), with mounting evidence supporting an important role for peripheral dysfunction, particularly within skeletal muscle. In patients with severe COPD and activity-matched controls, muscle oxygen transport and utilization were assessed at peak effort during single-leg knee-extensor exercise (KE), where ventilation is assumed to be submaximal. This strategy removes ventilation as the major constraint to exercise capacity in COPD, allowing maximal muscle function to be attained and evaluated. During maximal KE, both convective arterial oxygen delivery to the skeletal muscle microvasculature and subsequent diffusive oxygen delivery to the mitochondria were diminished in patients with COPD compared to control subjects. These findings emphasize the importance of factors, beyond the lungs, that influence exercise capacity in this patient population and may, ultimately, influence the prognosis, mortality and quality of life for patients with COPD. Peak oxygen uptake (V?O2peak), a primary determinant of prognosis, mortality and quality of life, is diminished in patients with chronic obstructive pulmonary disease (COPD). Mounting evidence supports an important role of the periphery, particularly skeletal muscle, in the diminished V?O2peak with COPD. However, the peripheral determinants of V?O2peak have not been comprehensively assessed in this cohort. Thus, the hypothesis was tested that both muscle convective and diffusive oxygen (O-2) transport, and therefore skeletal muscle peak O-2 uptake (V?MO2peak), are diminished in patients with COPD compared to matched healthy controls, even when ventilatory limitations (i.e. attainment of maximal ventilation) are minimized by using small muscle mass exercise. Muscle O-2 transport and utilization were assessed at peak exercise from femoral arterial and venous blood samples and leg blood flow (by thermodilution) in eight patients with severe COPD (forced expiratory volume in 1s (FEV1) +/- SEM = 0.9 +/- 0.1 l, 30% of predicted) and eight controls during single-leg knee-extensor exercise. Both muscle convective O-2 delivery (0.44 +/- 0.06 vs. 0.69 +/- 0.07 l min(-1), P < 0.05) and muscle diffusive O-2 conductance (6.6 +/- 0.8 vs. 10.4 +/- 0.9 ml min(-1) mmHg(-1), P < 0.05) were similar to 1/3 lower in patients with COPD than controls, resulting in an attenuated V?MO2peak in the patients (0.27 +/- 0.04 vs. 0.42 +/- 0.05 l min(-1), P < 0.05). When cardiopulmonary limitations to exercise are minimized, the convective and diffusive determinants of V?MO2peak, at the level of the skeletal muscle, are greatly attenuated in patients with COPD. These findings emphasize the importance of factors, beyond the lungs, that may ultimately influence this population's prognosis, mortality and quality of life.
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